Appleton, 1998, UK |
Process:
| • Overall: NR | • Standard: NHSBSP guidelines, 1991-1992 | • Inclusion: convenience sample mastectomy specimens
reports of invasive tumor, ALND issued by non-specialist
pathologists, 1992, 1994, & 1996 |
| • % reporting nature of specimenIV
| • by y: | • Data sources: pathology reports | • Exclusion: NR |
| | 1992: 60% | • Developmental period: NR | • Period: 4 y (1992-1996) |
| | 1994: 40% | • Reference standard(s) (publication date): NR | • n specimens (enrolled/evaluated): 40/30 (10 for each
y) |
| | 1996: 100% | • Data sources: NR | • Age (mean & range): NR |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % reporting type of tumorIV
| • Overall: NR | • Links to outcomes: NR | • Case characteristics: NR |
| | • by y: | • Funding source: NR | • Socioeconomic status: NR |
| | 1992: 100% | • State of use: NR | • Funding: NR |
| | 1994: 100% | • Current use: research; internal quality improvement;
quality of care reporting | |
| | 1996: 100% | • Care setting: pathology centers | |
|
| • Links: NA | • Professionals: pathologists | |
| • % reporting grade of tumorIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 90% | | |
| | 1994: 80% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting size of tumorIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 80% | | |
| | 1994: 70% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting number of involved & sampled
LNIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 100% | | |
| | 1994: 100% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting involvement of resection
marginsIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 90% | | |
| | 1994: 90% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting side of mastectomyIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 60% | | |
| | 1994: 50% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting size of specimen (macroscopic)
IV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 100% | | |
| | 1994: 90% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting of affected quandrant (gross exam)
IV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 80% | | |
| | 1994: 60% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting size of overlying skinIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 100% | | |
| | 1994: 100% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting distance of tumor from
nippleIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 50% | | |
| | 1994: 30% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting description of cut surface of
tumorIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 80% | | |
| | 1994: 80% | | |
| | 1996: 10% | | |
|
| • Links: NA | | |
| • % reporting description of skinIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 0% | | |
| | 1994: 20% | | |
| | 1996: 0% | | |
|
| • Links: NA | | |
| • % reporting description of nippleIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 50% | | |
| | 1994: 50% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting presence or absence of fascia or skeletal
muscleIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 0% | | |
| | 1994: 0% | | |
| | 1996: 10% | | |
|
| • Links: NA | | |
| • % reporting presence or absence of vascular
invasionIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 90% | | |
| | 1994: 60% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting involvement of apical LNIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 40% | | |
| | 1994: 80% | | |
| | 1996: 80% | | |
|
| • Links: NA | | |
| • % reporting distance of tumor to resection
marginsIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 100% | | |
| | 1994: 80% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting presence or absence of concurrent
DCISIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 100% | | |
| | 1994: 70% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting size of concurrent DCISIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 38% | | |
| | 1994: 33% | | |
| | 1996: 100% | | |
|
| • Links: NA | | |
| • % reporting description of background
breastIV
| • Overall: NR | | |
| | • by y: | | |
| | 1992: 90% | | |
| | 1994: 90% | | |
| | 1996: 80% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patient; enrolled = n qualified; evaluated = n analyzed; NHSBSP =
National Health Service Breast Screening Programme; LN = lymph
nodes; DCIS = ductal carcinoma in situ; state of use = last 3 y;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Bernhard, 1997,
Netherlands |
Process:
| • Overall: NR | • Standard: IBCSG form for assessing impact of adjuvant
therapy on QOL; LASA scales (physical well-being; mood;
appetite) | • Inclusion: convenience sample pre- &
postmenopausal women with operable BC |
| • Change in QOL by time & treatment arm;
postmenopausal women, node(-) BC who underwent adjuvant
therapyIa
| • Physical well-being: | • Data sources: pts self-reported status using IBCSG
form | • Exclusion: pts who completed no 1993 version QOL
forms; completed forms in multiple languages |
| | Tamoxifen: 83.4 (1 mo) | • Developmental period: NR | • Period: 2 y (1993-1995) |
| | Tmx + CM: 83.2 (1 mo) | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 345/312 |
| | Tamoxifen: 85.5 (3 mo) | • Data sources: NR | • Age (mean & range): (NR) |
| | Tmx + CMF: 78.2 (3 mo) | • Psychometric properties: NR | • Race/ethnicity: NR |
| | Tamoxifen: 86.5 (6 mo) | • Links to outcomes: NR | • Case characteristics: women with operable BC |
| | Tmx + CMF: 85.3 (6 mo) | • Funding source: NR | • Socioeconomic status: NR |
| | • Mood: | • State of use: NR | • Funding: ACS; NHMRC of Australia grants |
| | Tamoxifen: 78.8 (1 mo) | • Current use: research | |
| | Tmx + CMF: 78.2 (1mo) | • Care setting: hospitals; cancer centers; | |
| | Tamoxifen: 80.7 (3 mo) | • Professionals: oncologists | |
| | Tmx + CMF: 76.8 (3 mo) | | |
| | Tamoxifen: 81.8 (6 mo) | | |
| | Tmx +CMF: 82.0 (6 mo) | | |
| | • PACIS: | | |
| | Tamoxifen: 78.1(1 mo) | | |
| | Tmx + CMF: 71.2 (1 mo) | | |
| | Tamoxifen: 81.0 (3 mo) | | |
| | Tmx + CMF: 69.5 (3 mo) | | |
| | Tamoxifen: 80.8 (6 mo) | | |
| | Tmx + CMF: 78.7 (6 mo) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; PACIS =
Perceived Adjustment to Chronic Illness Scale; ACS = American Cancer
Society; NHMRC = National Health and Medical Research Council; state
of use = last 3 y; LASA = Linear analogue self-assessment; Higher
scores in scale = better quality of life; QOL = quality of life;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Bickell, 2000, US |
Process:
| • Overall: 59% | • Standard: Mount Sinai Health Final Guidelines for
Stage I & II BC treatment, 1994-1995 | • Inclusion: convenience sample women BC receiving
definitive surgical treatment of primary stage I or II in 4
hospitals in NY |
| • % appropriate use of BCSIV
| • by hospital: 49–69% | • Data sources: tumor registries; hospital discharge
& pathology databases from 4 teaching hospitals NY area | • Exclusion: treatment in other hospital; recurrent
cancers; males; DCIS |
|
| • Links: NA | • Developmental period: NR | • Period: 2 y (1995-1996) |
| • % appropriate use of RT after BCSIV
| • Overall: 81% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 1,258/723 |
| | • by hospital: 69–87% | • Data sources: NR | • Age (mean & range): 65 (NR) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: Black (5–12%) |
| • % appropriate use of adjuvant systemic treatment ,
stage ≥ 1BIV
| • Overall: 78% | • Links to outcomes: NR | • Case characteristics: stage I or II BC |
| | • by hospital: | • Funding source: NR | • Socioeconomic status: Medicaid 4–23% |
| | 71–86 % | • State of use: NR | • Funding: United Hospital Fund |
| | • by age: | • Current use: internal quality improvement; external
quality oversight; research | |
| | <50 y: 59–87% | • Care setting: hospitals; cancer centers; RT
centers | |
| | ≥50 y: 65–85% | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
| • Links: NA | | |
| • % appropriate use of ALNDIV
| • Overall: 87% | | |
| | • by hospital: 79–92% | | |
|
| • Links: NA | | |
| • % quality of hormone receptor assayIV
| • Overall: 85% | | |
| | • by hospital: 56–99% | | |
|
| • Links: NA | | |
|
Access:
| • Overall: 64% | | |
| • % referral to oncologistIV
| • by hospital: 50–81% | | |
|
| • Links: NA | | |
| • % evidence of surgical options
discussionIV
| • Overall: NR | | |
| | • by hospital: 65–100% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast- conserving surgery; RT =
radiotherapy; GP = general practitioner; NY = New York; DCIS =
ductal carcinoma in situ; state of use = last 3 y; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Bickell, 2003, US |
Structure:
| • Overall: 32% (14/44) | • Standard: Mount Sinai Health Final Guidelines for
Stage I–II BC treatment, 1994-1995 | • Inclusion: convenience sample women ESBC who had
under-use of treatment; RT or adjuvant therapy not recommended when
indicated |
| • % cases not receiving recommended treatment (RT after
BCS or systemic therapy) due to system failureIV
| • Links: NA | • Data sources: Interview of 13 surgeons who treated
pts | • Exclusion: NR |
| | | • Developmental period: NR | • Period: 2 y (1998-1999) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): NR/44 |
| | | • Data sources: NR | • Age (mean & range): NR |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: stage I or II BC |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Department of Health Policy, Mount Sinai
School of Medicine & the Mount Sinai NYU Health System |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; RT =
radiotherapy; GP = general practitioner; state of use = last 3 y; BC
= breast cancer; MD = medical doctor; NYU = New York University;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Bower, 2000, US |
Outcome:
| • Overall: NR | • Instrument(s): RAND 36-item Health Survey 1.0
(physical; role function-physical; body pain; social functioning;
emotional well-being; role function-emotional; energy/fatigue;
general health perceptions) | • Inclusion: convenience sample women ESBC (stage
0–II); diagnosed <5 y; completed adjuvant therapy; currently
disease-free; only treated with tamoxifen (cancer survivors) |
| • % change in QOL over timeIac
| • Energy/fatigue: 60 | • Data sources: tumor registry; medical records;
self-reported questionnaires | • Exclusion: no English-spoken |
| | • Physical functioning: 80.35 | • Developmental period: NR | • Period: 3 y (1994-1997) |
| | • Role limitation- physical: 75.80 | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): NR/1,957 |
| | • Emotional well-being: 75 | • Data sources: NR | • Age (mean & range): 55 (NR) y |
| | • Role limitation- emotional: 77 | • Psychometric properties: NR | • Race/ethnicity: White (80%); Black (12.5%) |
| | • Social functioning: 86 | • Links to outcomes: NR | • Case characteristics: BC survivors; currently
tamoxifen (47.5%) |
| | • Bodily pain: 78.60 | • Funding source: NR | • Socioeconomic status: married (70%); employed (45%);
income/ y > U$ 75,000 (36.5%) |
| | • General health: 73 | • State of use: NR | • Funding: NCI |
| | • Links: NA | • Current use: external quality oversight;
research | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; QOL =
quality of life; state of use = last 3 y; GP = general practitioner;
NCI = National Cancer Institute; ESBC = early stage breast cancer;
RT = radiotherapy; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Brenin, 1999, US | • % appropriate use of axillary lymph node
dissectionIV
| • Overall: 93.2% (n = 15,992) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: national convenience sample women BC,
stage I or II treated in US hospitals, 1994 |
| | • by age (y): | • Data sources: National Cancer Data Base | • Exclusion: not eligible; stage III or IV;
subcutaneous mastectomy; not lymph nodes examined undergoing
ALND |
| | <70: 97% | • Developmental period: NR | • Period: 1 y (1994) |
| | >70: 86% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 17,931/17,151 |
| | • by payer: | • Data sources: NR | • Age (mean & range): 61.3 (22 –103) y |
| | Private vs. Government: OR 1.4 S | • Psychometric properties: NR | • Race/ethnicity: NR |
|
| • Links: NA | • Links to outcomes: NR | • Case characteristics: women BC stage I or II; node
(+) 5.2%; |
| • % appropriate use of BCSIV
| • Overall: 44.5% | • Funding source: NR | • Socioeconomic status: NR |
|
| • Links: NA | • State of use: NR | • Funding: CCACS; ACR |
| • % appropriate use of RT on axillaIV
| • Overall: 5.2% (n = 899) | • Current use: external quality oversight; research;
decision-making | |
| | • Links: NA | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: clinicians; oncologists; RT
oncologists; surgeons | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; RT =
radiotherapy; DCIS = ductal carcinoma in situ; BC = breast cancer;
CCACS = Commission on Cancer of the American College of Surgeons;
ACR = American College of Radiology; BCS = breast-conserving
surgery; NIH = National Institute of Health; ALND = axillary lymph
node dissection; state of use = last 3 y; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Cheung, 1999, Hong
Kong |
Process:
| • Overall: 32% | • Standard: BASO guidelines, 1995 | • Inclusion: convenience sample women on whom author
operated post CPG; women operable primary BC <5 cm; for BCS
only tumor size, 3 cm |
| • % appropriate use of
BCSIV
| • Links: NA | • Data sources: medical records | • Exclusion: NR |
| • % appropriate use of mastectomyIV
| • Overall: 68% | • Developmental period: NR | • Period: NR |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 100/100 |
| • % appropriate use of CTIV
| • Overall: 30% | • Data sources: NR | • Age (mean & range): 53 (25–83) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of tamoxifenIV
| • Overall: 28% | • Links to outcomes: NR | • Case characteristics: BC Grade I–III; node (-) (57%);
invasive ductal (72%); vascular invasion (34%); ER (+) (58%) |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % (>90%) quality of FNA samples from lesions
which subsequently prove to be BC should be adequate as deemed by
the breast pathologistIV
| • Overall: 99% | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: internal quality improvement;
research | |
| • % (90%) appropriate use of cytology or needle
histology in palpable BC diagnosed pre-operatively IV
| • Overall: 82% | • Care setting: hospitals; cancer centers; RT
centers | |
|
| • Links: NA | • Professionals: GPs; oncologists; surgeons | |
| • % (<10%) quality of breast biopsy: primary
operable BC receives frozen sectionIV
| • Overall: 0% | | |
|
| • Links: NA | | |
| • % gross margins identified without incision into de
specimen; & carefully orientated for the
pathologistIV
| • Overall: 100% | | |
|
| • Links: NA | | |
| • % (90%) appropriate number of therapeutic operations
(≤2) for women having BCSIV
| • Overall: 100% | | |
|
| • Links: NA | | |
| • % quality of technique to determine histological node
status for all invasive tumors, by sampling or
clearanceIV
| • Overall: 100% | | |
|
| • Links: NA | | |
|
Access:
| • Overall: 95% | | |
| • % (>80%) urgent
referrals seen within 5 working d of referral receiptIV
| • Links: NA | | |
| • % (70%) all other new referrals seen within 15
working dIV
| • Overall: 50% | | |
|
| • Links: NA | | |
| • % appropriate use of imaging &/or cytology or
needle biopsy, if required; to be performed at the initial
visitIV
| • Overall: 0% | | |
|
| • Links: NA | | |
| • % (<10%) all new women BC should attend the
clinic/hospital on >2 occasions for diagnostic
purposesIV
| • Overall: 41% | | |
|
| • Links: NA | | |
| • % pts attending for diagnostic purposes seen at least
on 1 occasion by breast specialist surgeonIV
| • Overall: 100% | | |
|
| • Links: NA | | |
| • %(>90%) women requiring an operation for
diagnostic purposes should be admitted 14 d of investigations
leading to surgical decisionIV
| • Overall: 68% | | |
|
| • Links: NA | | |
| • %(>90%): BC pts or an abnormality requiring
diagnostic operation; told within 5 working d leading
diagnosisIV
| • Overall: 67% | | |
|
| • Links: NA | | |
| • % (100%) BC pts given opportunity to see a BC
nurseIV
| • Overall: 100% | | |
|
| • Links: NA | | |
| • % (90%) women admitted for operation within 21 d of
surgical decision to operate for therapeutic purposesIV
| • Overall: 93% | | |
|
| • Links: NA | | |
|
Outcome:
| • Overall: 0% | | |
| • % (<10%) pts developing
local recurrence after BCS within 5 yIV
| • Links: NA | | |
| • % (<10%) pts developing local recurrence after
mastectomy within 5 yIV
| • Overall: 2.6% | | |
| | • Mastectomy cases: 36% | | |
|
| • Links: NA | | |
| • % appropriate use of prophylactic RT employed in
women with high risk of flap recurrenceIV
| • Overall: 2% (36% of mastectomies 7) | | |
|
| • Links: NA | | |
| • % (<10%) regional recurrence needing further
surgery or RT; at 5 yIV
| • Overall: 0% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; CT =
chemotherapy; RT = radiotherapy; HT = hormone therapy; GP = general
practitioner; ER = estrogen receptor; PR = progesterone receptor;
CPG = clinical practice guidelines; DCIS = ductal carcinoma in situ;
BC = breast cancer; BASO = British Association of Surgical Oncology;
FNA = fine-needle aspiration; state of use = last 3 y; BCS =
breast-conserving surgery; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Chie, 1999, China |
Outcome:
| • Overall: NR | • Instrument(s): SF-36 Chinese version;
EORTC-QLQ-C30* | • Inclusion: convenience sample women diagnosed or
treated for BC in breast surgery; RT & oncology outpatients
departments; or in general surgical wards of National Taiwan
University Hospital |
| • % women with significant improvement in QOL scores in
clinical phases of BC: diagnosis; surgery; initial CT; initial RT;
follow-up; recurrence**Iac
| • Links: NA | • Data sources: self- reported questionnaires to pts
before RT (pretest); after RT (post-test) & recall of
pretest; cancer registry | • Exclusion: high-dose regimens that necessitated
hospitalization & terminal pts in palliative care unit |
| | | • Developmental period: NR | • Period: 2 mo (1997) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 115/115 |
| | | • Data sources: NR | • Age (mean & range): NR
(<40–>65) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: clinical phases: diagnosis
(35.7%); surgery (9.6%); initial CT (13%); initial RT (7%);
follow-up after treatment (27.8%); recurrence (7%) |
| | | • Funding source: NR | • Socioeconomic status: married (73.9%); employed
(50.4%%) |
| | | • State of use: NR | • Funding: NR |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; RT =
radiotherapy; CT = chemotherapy; QOL = quality of life;
EORTC-QLQ-C30 = European Organization for Research and Treatment of
Cancer Quality of Life Questionnaire - cancer 30; SF-36 = medical
outcome survey 36-item short form health surveys; state of use =
last 3 y; * Validated for BC patients; **Includes: Role functioning;
emotional functioning; cognitive functioning; global quality of
life; nausea & vomiting; loss of appetite; constipation; GP
= general practitioner; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Christensen, 2002,
Denmark |
Process:
| • Overall: 100% | • Standard: European Guidelines for Quality Assurance
in Mammography screening, 1996; Guidelines for cytology procedures
and reporting in BC screening, 1993 | • Inclusion: women with (+) mammography screening
followed by surgery |
| • % appropriate use of preoperative diagnosis by FNA
cytology, needle histology or biopsyIV
| • Links: NA | • Data sources: hospital registries of Copenhagen
(pathology & mammography screening program) | • Exclusion: data missing; lymphoma |
| | | • Developmental period: NR | • Period: 6 y (1991-1997) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 4,111/4,111 |
| | | • Data sources: NR | • Age (mean & range): 61 (50–72) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: NR |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: NR |
| | | • Current use: internal quality improvement; external
quality oversight | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists; pathologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; NCI =
National Cancer Institute; state of use = last 3 y; FNA = fine-
needle aspiration; FP = false positive; FN = false negative; BC =
breast cancer; (+) = positive; GP = general practitioner; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Cochrane, 1997, UK |
Process:
| • Overall: 60% | • Standard: NHSBSP breast referral guidelines,
1995 | • Inclusion: random sample women > 35 y with
breast problems referred to surgeon by GP in Rapid Access Breast
Clinic in Cardiff, UK |
| • % appropriate use of referrals to surgeon by GP
according to breast referral guidelinesIV
| • by age: | • Data sources: referral database | • Exclusion: screening cases; tertiary referrals;
abnormal Mx |
| | <40 y: 54% | • Developmental period: NR | • Period: 8 mo (1995) |
| | >40 y: 64% S | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 2,332/2,332 |
| | • Links: NA | • Data sources: NR | • Age (mean & range): 44 (11–90) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: women with BC symptoms: lumps
(60%); pain (32%); nipple discharge (8%); skin change (5.2%) |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Patterns of Care Study |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: surgeons; oncologists; RT oncologists;
GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; enrolled = n qualified; evaluated = n
analyzed; RT = radiotherapy; state of use = last 3 y; Mx =
mammogram; NHSBSP = NHS Breast Screening Programme; GP = general
practitioner; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Cornfeld, 2001, US |
Structure:
| • Overall: 100% | • Standard: NCCN Guidelines, 1999 | • Inclusion: convenience sample women with
nonmetastatic BC treated in private practice of 11 oncologists
surveyed |
| • % board certified MDs in
medical oncologyIV
| • Links: NA | • Data sources: survey delivered to private practice
oncologists (n = 11); medical records | • Exclusion: NR |
| • % availability of office procedure manual used for CT
administrationIV
| • Overall: 100% | • Developmental period: NR | • Period: 9 mo (1999-2000) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n participants (enrolled/evaluated): NR/220 |
| • % documentation of CME credits 2 y preceding each
auditIV
| • Overall: 100% | • Data sources: NR | • Age (mean & range): NR |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % present CT flow sheets on active treatment
chartsIV
| • Overall: 99% | • Links to outcomes: NR | • Case characteristics: NR |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
|
Process:
| • Overall: 90% | • State of use: NR | • Funding: NR |
| • % present body surface area
calculations on CT flow sheetsIV
| • Links: NA | • Current use: internal quality improvement | |
| • % appropriate use of tamoxifen BC ER (+)IV
| • Overall: 100% | • Care setting: hospitals; cancer centers | |
|
| • Links: NA | • Professionals: oncologists; surgeons | |
| • % appropriate use of guidelines for follow-up
surveillance of BCIV
| • Overall: NR | | |
| | • by practice: | | |
| | PE: 100% | | |
| | Mammography: 98% | | |
| | Gynecologic follow-up: 76% | | |
|
| • Links: NA | | |
|
Outcome:
| • Overall: 4.91* | | |
| • % participation of oncologists in pts satisfaction
surveyIV
| • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; CT =
chemotherapy; CME = continuing medical education; BC = breast
cancer; HT = hormone therapy; ER (+) = estrogen receptor positive;
SD = standard deviation; * = number of participants were 3; state of
use = last 3 y; NCCN = National Comprehensive Cancer Network; PE =
physical examination; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Craft, 2000,
Australia |
Process:
| • Overall: 98% (85/87) | • Standard: NHMRC CPG for the management of early BC,
1995 | • Inclusion: convenience sample women newly diagnosed
primary localized invasive BC treated in ACT, 1997-1998 |
| • % appropriate use of RT after
BCSIV
| • Links: NA | • Data sources: dataset of survey conducted by the
Provincial Surgeons of Australia; pathology reports; treatment
facility records | • Exclusion: males; distant metastases; in situ |
| • % appropriate use of ALND for invasive
BCIV
| • Overall: 91% (173/190) | • Developmental period: NR | • Period: 14 mo (1997-1998) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 217/191 |
| • % appropriate use of some form of adjuvant systemic
therapy in node (+) or tumor >2 cmIV
| • Overall: 96% (95/99) | • Data sources: NR | • Age (mean & range): 57 (25–88) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of adjuvant CT in <50 y;
node (+)IV
| • Overall: 100% (27/27) | • Links to outcomes: NR | • Case characteristics: women premenopausal (29%);
postmenopausal (57%); invasive BC (93%); HR (+) (81%); tumor size
1.1–2 cm (43%); node (-) (56%); tumor type (invasive ductal) grade 2
(35%) |
| | • Links: NA | • Funding source: NR | • Socioeconomic status: urban (67%) |
| | | • State of use: NR | • Funding: Commonwealth Department of Health and Aged
Care Cancer Screening Unit |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: surgeons; RT oncologists; oncologists;
pathologists; nurses | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; BCS = breast-conserving surgery; ALND
= axillary lymph node dissection; ACT = Australian capitol
territory; enrolled = n qualified; evaluated = n analyzed; NHMRC =
National Health and Medical Research Council; CPG = clinical
practice guideline; CT = chemotherapy; RT = radiotherapy; state of
use = last 3 y; HR = hormone receptor; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
DeMichele, 2003, US |
Process:
| • Overall: 74% (156/208) | • Standard: St. Gallen Consensus Conference, 1992-1995
(update)* | • Inclusion: convenience sample women BC ≥ 50 y
evaluated at UPCC 1993-1997 & eligible for adjuvant
chemotherapy |
| • % appropriate use of CT (recommended)IV
| • by age: | • Data sources: University of Pennsylvania pt
information system database | • Exclusion: missing data |
| | 50–54 y: 98% (57/58) | • Developmental period: NR | • Period: 5 y (1993-1997) |
| | 55–60 y: 85% (47/55) | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 367/208 |
| | 61–69 y: 52% (40/52) | • Data sources: NR | • Age (mean & range): 59(50–86) y |
| | 70+: 23% (10/43) | • Psychometric properties: NR | • Race/ethnicity: NR |
|
| • Links: NA | • Links to outcomes: NR | • Case characteristics: women BC node (+) (61%);
ER&PR (+) (46%); tumor size T1 (47%) |
| • % non–eligible pts receiving CT (over
treatment)IV
| • Overall: 11% (23/132) | • Funding source: NR | • Socioeconomic status: NR |
|
| • Links: NA | • State of use: NR | • Funding: NR |
| • % appropriate use of CT (received) (patient
acceptance)IV
| • Overall: 74% (154/208) | • Current use: external quality oversight | |
| | • by age: | • Care setting: cancer centers; hospitals; RT
centers | |
| | 50–59 y: 74% (72/97) | • Professionals: oncologists; surgeons; RT
oncologists | |
| | 60–69 y: 74% (36/47) | | |
| | 70–86 y: 70% (7/10) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; RT = radiotherapy; HR = hormone receptor; state of use =
last 3 y; UPCC = University of Pennsylvania Cancer Center; ER =
estrogen receptor; PR = progesterone receptor; BC = breast cancer;
*Recommendations for women <65 y; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Du, 2001, US |
Process:
| • Overall: 12.4% (708/5,697) | • Standard: NIH Consensus Conference Development,
1990 | • Inclusion: population-based sample women ≥ 65 y
diagnosed BC, 1991-1996 |
| • % appropriate use of CT within 6 mo of
diagnosisIV
| • by Stage (1996): | • Data sources: SEER registry; Medicare claim data | • Exclusion: women with no full coverage of Medicare;
members of HMO |
| | I: 3% | • Developmental period: NR | • Period: 6 y (1991-1996) |
| | II: 19.5% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 35,060/5,697 |
| | III: 43.7% | • Data sources: NR | • Age (mean & range): NR (>65) y |
| | IV: 40.9% | • Psychometric properties: NR | • Race/ethnicity: NR |
| | • by age: | • Links to outcomes: NR | • Case characteristics: women BC stage I–IV; >
65 y |
| | 65–69 y: 20.5% | • Funding source: NR | • Socioeconomic status: Medicare 100% |
| | 70–74 y: 13.9% | • State of use: NR | • Funding: Department of Defense; NCI; Sealy &
Smith Foundation |
| | 75–79 y: 8.7% | • Current use: external quality oversight | |
| | >80 y: 3.3% | • Care setting: hospitals; cancer centers | |
|
| • Links: NA | • Professionals: oncologists; surgeons; GPs | |
| • % appropriate use CT in node (+); ER (+); within 6 mo
of diagnosisIV
| • Overall: 27% (1996) | | |
|
| • Links: NA | | |
| • % appropriate use CT in node (+); ER (-); within 6 mo
of diagnosisIV
| • Overall: 61.5% (1996) | | |
|
| • Links: NA | | |
| • % appropriate use CT in node (-); ER (+); within 6 mo
of diagnosisIV
| • Overall: 2% (1996) | | |
|
| • Links: NA | | |
| • % appropriate use CT in node (-); ER (-); within 6 mo
of diagnosisIV
| • Overall: 17.9% (1996) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; state of use = last 3 y; GP = general practitioner;
NCI = National Cancer Institute; SEER = Surveillance, Epidemiology,
and End Results; CT = chemotherapy; HMO = Health Maintenance
Organization; ER = estrogen receptor; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Du, 2003, US
|
Process:
| • Overall: 28.7% | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: population-based sample women ≥20 y stage
I–IIIA BC treated & registered in New Mexico tumor registry,
1991-1997 |
| • % appropriate use of CTIV
| • by stage: | • Data sources: New Mexico tumor registry; pathology
laboratories & hospitals in New Mexico | • Exclusion: stage other than I–IIIA, <20 y |
| | I: 11.3% | • Developmental period: NR | • Period: 7 y (1991-1997) |
| | II: 47% | • Reference Standard(s) (Publication Date): NR | • n patients (enrolled/evaluated): NR/5, 101 |
| | IIIA: 68% | • Data sources: NR | • Age (mean & range): 61(20–98) y |
| | • by age: | • Psychometric properties: NR | • Race/Ethnicity: NR |
| | <45 y: 66% | • Links to outcomes: NR | • Case characteristics: NR |
| | 45–49 y: 54.9% | • Funding source: NR | • Socioeconomic status: NR |
| | 50–54 y: 44.2 % | • State of use: NR | • Funding: NCI, NIH, Smyth Foundation |
| | 55–59 y: 31% | • Current use: internal quality improvement | |
| | 60–64 y: 18.1% | • Care setting: hospitals; cancer centers | |
| | 65–69 y: 12.3% | • Professionals: oncologists | |
| | 70–74 y: 7.1% | | |
| | > 75 y: 3.4% | | |
|
| • Links: NA | | |
| • % appropriate use of CT + HT (tamoxifen)
IV
| • Overall: 9.6% | | |
| | • by age: | | |
| | <45 y: 15.8% | | |
| | 45–49 y: 17% | | |
| | 50–54 y: 18.5 % | | |
| | 55–59 y: 11.7% | | |
| | 60–64 y: 8% | | |
| | 65–69 y: 5.4% | | |
| | 70–74 y: 4.0% | | |
| | > 75 y: 0.8% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; NCI =
National Cancer Institute; NIH = National Institute of Health; CT =
chemotherapy; BC = breast cancer; CPG = clinical practice guideline;
state of use = last 3 y; HT = hormone therapy; Level Ia = pre-study
data indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Edge, 2002, US |
Process:
| • Overall: 63.4% (294/464) | • Standard: NIH Consensus Development Conference 1990;
Steering committee on CPGs for the care & treatment of BC,
CARO | • Inclusion: convenience sample women ≥67 y stage T1–T2
(N0N1) M0, newly diagnosed histologically confirmed invasive BC who
underwent BCS |
| • % appropriate use of ALND after BCSIV
| • by age: | • Data sources: pt interviews; medical records | • Exclusion: DCIS; bilateral, multicentric, locally
advanced disease; incomplete data; history of prior or secondary BC;
surgery other than BCS |
| | 67–69 y: 84% | • Developmental period: NR | • Period: 2 y (1995-1997) |
| | 70–74 y: 73% | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 1,377/464 |
| | 75–79 y: 62% | • Data sources: NR | • Age (mean & range): NR |
| | > 80 y: 33% S | • Psychometric properties: NR | • Race/ethnicity: White (91%); Black (9%) |
| | • by race/ethnicity: | • Links to outcomes: NR | • Case characteristics: stage I (84.9%); stage IIA
(9%); stage IIB (1.7%); HR (+) (69.4%) |
| | White: 64% | • Funding source: NR | • Socioeconomic status: education: < High school
(66.4%); HMO (73.2%) |
| | Black: 60 % NS | • State of use: NR | • Funding: AHRQ & Department of the Army
grants |
| | • by education: | • Current use: decision-making; external quality
oversight | |
| | < High school: 60% | • Care setting: hospitals; pathology centers | |
| | ≥ High school: 66% | • Professionals: oncologists; surgeons; RT oncologists;
GPs | |
| | • by Payer: | | |
| | HMO: 64% | | |
| | Private: 65% | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCSIV
| • Overall: 77.8% (361/464) | | |
| | • With ALND 54.7% | | |
|
| • Links: NA | | |
| • % appropriate use of adjuvant systemic therapy after
BCSIV
| • Overall: 70.7% (328/464) | | |
| | • by treatment: | | |
| | CT: 10.1% | | |
| | Tamoxifen: 89.9% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; BCS = breast-conserving surgery; ALND
= axillary lymph node dissection; NIH = National Institute of
Health; CARO = Canadian Association of Radiation Oncologists; GP =
general practitioner; MO = non-metastatic; DCIS = ductal carcinoma
in situ; RT = radiotherapy; state of use = last 3 y; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Engel, 2002, Germany |
Process:
| • Overall: NR | • Standard: NIH Consensus Development Conference, 1990;
St. Gallen's Consensus for adjuvant systemic therapy, 1995-1998
(update) | • Inclusion: convenience sample women any stage BC
residing in one of 6 regions*, Germany |
| • % appropriate use of BCSIV
| • by region: 39.3%–57.7% | • Data sources: data submitted by pathologists,
gynecologists, surgeons & radiologists, 6 regions in
Germany | • Exclusion: NR |
|
| • Links: NA | • Developmental period: NR | • Period: 3 y (1996-1998) |
| • % appropriate use of RT after BCSIV
| • Overall: NR | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 9,210/8,661 |
| | • by region: 80.6%–85.0% | • Data sources: NR | • Age (mean & range): NR
(<50–>70) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of RT after mastectomyIV
| • Overall: NR | • Links to outcomes: NR | • Case characteristics: HR (+) 80%; stage 0–IV; LN
status known |
| | • by region: 10.4%–32.2% | • Funding source: NR | • Socioeconomic status: NR |
|
| • Links: NA | • State of use: NR | • Funding: German Federal Ministry of Health |
| • % appropriate use of CT in premenopausal; node (+);
HR (+) (1995) IV
| • Overall: NR | • Current use: external quality oversight;
decision-making; quality of care reporting; research | |
| | • by region: 42.9%–84.6% | • Care setting: hospitals; cancer centers; RT
centers | |
|
| • Links: NA | • Professionals: oncologists; RT oncologists; surgeons;
GPs | |
| • % appropriate use of CT & HT in
premenopausal; node (+); HR (+) (1995-1998) IV
| • Overall: NR | | |
| | • by region: 10.3%–57.1% | | |
|
| • Links: NA | | |
| • % appropriate use of CT in premenopausal; node (+);
HR (-) (1995/1998) IV
| • Overall: NR | | |
| | • by region: 63.6%–92.3% | | |
|
| • Links: NA | | |
| • % appropriate use of tamoxifen in postmenopausal;
node (+); HR (+) (1995) IV
| • Overall: NR | | |
| | • by region: 30.1%–61.5% | | |
|
| • Links: NA | | |
| • % appropriate use of CT & HT in
postmenopausal; node (+); HR (+) (1995/1998) IV
| • Overall: NR | | |
| | • by region: 9.1%–32.2% | | |
|
| • Links: NA | | |
| • % appropriate use of CT in postmenopausal; node (+);
HR (-) (1995/1998) IV
| • Overall: NR | | |
| | • by region: 38.5%–69.6% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; HR (+) = hormone receptor positive; ER (-) = hormone
receptor negative; FI = family income; BCS = breast-conserving
surgery; RT = radiotherapy; CT = chemotherapy; HT = hormone therapy;
node (+) = lymph node positive; NIH = national health institute;
state of use = last 3 y; GP = general practitioner; *6 regions =
Aachen; Dresden; Jena; Marburg; Munich; Stuttgart; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Foroudi, 2002 Canada | • % appropriate use of RTIV
| • Overall: 56.3%–72.4%* | • Standard: North American CPG (n = 12); others | • Inclusion: population-based sample women with BC
eligible for RT from North American population |
| | • Initial: 50%–59.2%* | • Data sources: North American population- based cancer
registries (SEER & Ontario Cancer registry); National Cancer
database; single institutions; multi-institution databases | • Exclusion: NR |
| | • Later: 6.3%–13.3%* | • Developmental period: NR | • Period: NR |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): NR |
| • % appropriate use of RT; in situ; moderate risk,
prefer BCT (i) IV
| • Overall: 37.7%* | • Data sources: NR | • Age (mean & range): NR |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of RT: stage I & II (pN0),
prefer BCT ; receiving BI (i) IV
| • Overall: NR | • Links to outcomes: NR | • Case characteristics: NR |
| | • Stage I: 57%* | • Funding source: NR | • Socioeconomic status: NR |
| | • Stage II: 52.2%* | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: internal quality improvement; external
quality oversight, decision-making; research | |
| • % appropriate use of RT: stage I &II (pN0),
postmastectomy, R1 or 2, receiving RI (i) IV
| • Overall: NR | • Care setting: hospitals; cancer centers; RT
centers | |
| | • Stage I: 0.6–0.8%* | • Professionals: surgeons; oncologists; RT oncologists;
GPs | |
| | • Stage II:0. 77–0.83 | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1);
<4N(+); postmastectomy, R1 or 2, receiving RI (i)
IV
| • Overall: 0.3%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1);
<4N(+); postmastectomy, R0, receiving RI (i) IV
| • Overall: 3.9–4.2%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1);
>3N(+); postmastectomy, receiving RI (i) IV
| • Overall: 5.7–6.1%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1), prefer BCT,
receiving BI (i) IV
| • Overall: 31.1%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IIIB (pT4 or pN3),w/wo
mastectomy, receiving RI (i) IV
| • Overall: 42%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT stage IIIA, < 4N(+),
postmastectomy, R1 or 2; receiving RI (i) IV
| • Overall: 0.24–0.35%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IIIA; < 4N(+),
postmastectomy; R0, prefer BCT; receiving RI (i) IV
| • Overall: 3.5–5.1%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IIIA; >3N(+),
postmastectomy, receiving RI (i) IV
| • Overall: 5.1–7.4%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IIIA; prefer BCT,
receiving BI (i) IV
| • Overall: 27.8%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IV, brain metastases
at diagnosis, receiving PRT (i) IV
| • Overall: 1.8%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IV; symptomatic bone
metastasis at diagnosis; receiving PRT (i) IV
| • Overall: 10%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: LCIS; recur with DCIS or
invasive carcinoma; receiving BI (r) IV
| • Overall: 0.7%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: DCIS, post-BCS, recur with
DCIS or invasive carcinoma; receiving BI (r) IV
| • Overall: 1.2%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: DCIS, postmastectomy;
locoregional relapse, receiving RI (r) IV
| • Overall: 0. 02–0.1%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage I & II (pN0),
postmastectomy, receiving PRT (r) IV
| • Overall: 2.9–4.2%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage I & II (pN0),
postmastectomy, locoregional relapse; receiving RI (r) IV
| • Overall: NR | | |
| | • Stage I: 1.3–1.9%* | | |
| | • Stage II: 1.7–1.9%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1);
postmastectomy; receiving PRTIV
| • Overall: 0.5%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage II (pN1);
postmastectomy (locoregional relapse); receiving RI (r)
IV
| • Overall: 1.35%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage III; postmastectomy;
receiving PRT (r) IV
| • Overall: 0.39–0.57%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage III; postmastectomy;
locoregional relapse; receiving RI (r) IV
| • Overall: 1.2–1.7%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IV, delayed symptoms
from bone metastasis; receiving PRT (r) IV
| • Overall: 10.4–21.7%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IV, delayed brain
metastasis; receiving PRT (r) IV
| • Overall: 4.8–10%* | | |
|
| • Links: NA | | |
| • % appropriate use of RT: stage IV, delayed cord
compression; receiving PRT (r) IV
| • Overall: 0.4–0.8%* | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; LN = lymph
nodes; BCS = breast conserving surgery; RT = radiotherapy; HR =
Hormone receptor; CI = contraindication; CT = chemotherapy; HT =
hormone therapy; CPG = clinical practice guidelines; BI = breast
irradiation; BCT = breast-conserving therapy; R0 = no residual
tumor; R1 = microscopic residual tumor; R2 = macroscopic residual
tumor; RI = radiation therapy; (i) = initial treatment; PRT = any
palliative RT; LCIS = lobular carcinoma in situ; (r) = progression
or relapse; state of use = last 3 y; GP = general practitioner; *
Estimates of the rate in a decision-making tree analysis; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Frazer, 1998 US |
Outcome:
| • Overall: NS changes over time in all subscales
& overall. | • Instrument: 39-item Guttman scaled HSQ Questionnaire
form (health perception; social & physical functioning;
physical & emotional role limitations; mental health; bodily
pain; energy-fatigue) | • Inclusion: convenience sample women ESBC diagnosed,
1993, & treated by surgery & HT at MDACCO, Orlando,
Florida |
| • % change (improvement) in QOL over timeIac
| • Links: NA | • Data sources: pts self-reported status using Guttman
scaled HSQ questionnaire form | • Exclusion: non-responders |
| | | • Developmental period: NR | • Period: 3 y (1993-1996) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): NR/70 |
| | | • Data sources: NR | • Age (mean & range): 61.4 (37–80) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: ESBC women with operable BC;
treated by surgery & HT |
| | | • Funding source: NR | • Socioeconomic status: married; not employed; HMO |
| | | • State of use: NR | • Funding: NR |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: oncologists; surgeons | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; HSQ = Health Status Questionnaire; MDACCO
= M.D. Anderson Cancer Center Orlando; state of use = last 3 y; HT =
hormone therapy; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Guadagnoli 1997, US |
Process:
| • Overall: 62% | • Standard: EBCTCG meta-analysis, 1992 | • Inclusion: convenience sample postmenopausal women
newly diagnosed invasive ESBC; stage I–II at 30 hospitals,
Minnesota, 1993 |
| • % appropriate use of any adjuvant systemic therapy in
node (-)IV
| • by age: | • Data sources: medical records; interviews | • Exclusion: diagnosis of carcinoma in situ;
inflammatory cancer; bilateral synchronous carcinoma; premenopausal
women |
| | 50–59 y: 73% | • Developmental period: NR | • Period: 1 y (1993) |
| | 60–69 y: 67% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 746/632 |
| | 70–79 y: 56% | • Data sources: NR | • Age (mean & range): NR (50–>80) y |
| | >80 y: 36% S | • Psychometric properties: NR | • Race/ethnicity: NR |
|
| • Links: NA | • Links to outcomes: NR | • Case characteristics: tumor size >1 cm (67%);
node (+) (25%); LVN (9%); ER (+) (64%) |
| • % appropriate use of tamoxifen in node
(-)IV
| • Overall: 51% | • Funding source: NR | • Socioeconomic status: married (54%); income >
$30,000 (70%); HMO (37%) |
| | • by age: | • State of use: NR | • Funding: NCI |
| | 50–59 y: 52% | • Current use: external quality oversight | |
| | 60–69 y: 55% | • Care setting: hospitals | |
| | 70–79 y: 51% | • Professionals: medical oncologists; oncological
radiologists | |
| | >80 y: 34% S | | |
|
| • Links: NA | | |
| • % appropriate use any adjuvant systemic therapy in
node (+)IV
| • Overall: 92% | | |
| | • by age: | | |
| | 50–59 y: 93% | | |
| | 60–69 y: 96% | | |
| | 70–79 y: 89% | | |
| | >80 y: 85% NS | | |
|
| • Links: NA | | |
| • % appropriate use any adjuvant systemic therapy in
node (+) BCIV
| • Overall: 71% | | |
| | • by age | | |
| | 50–59 y: 61% | | |
| | 60–69 y: 70% | | |
| | 70–79 y: 81% | | |
| | >80 y: 74% S | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; NCI = National Cancer Institute; EBCTCG = early
breast cancer trialists’ collaborative group; HT = hormone therapy;
CT = chemotherapy; state of use = last 3 y; ESBC = early-stage BC;
LVN = lymphatic- vessel invasion; ER = estrogen receptor; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Guadagnoli, 1998a US, |
Process:
| • Overall: 84% (MA) 86% (MN) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: convenience sample women ESBC (stage I or
II) in 2 states of US (MA & MN), 1993-1995 |
| • % appropriate use of RT after BCSIV
| • by age (OR): | • Data sources: hospital tumor registries; medical
records; patient survey; patient income & education US
census data; physician survey | • Exclusion: DCIS; bilateral synchronous BC;
inflammatory carcinoma |
| | 50–59 y: 0.4 S (MA); 4.2 NS (MN) | • Developmental period: NR | • Period: 2 y (1993-1995) |
| | 60–69 y: 0.5 NS (MA); 2.6 NS (MN) | • Reference standard(s) (publication sate): NR | • n patients (enrolled/evaluated): 2,575/2,575 (MA =
1,514; MN = 1,061) |
| | 70–79 y: 0.3 S (MA); 0.3 NS (MN) | • Data sources: NR | • Age (mean & range): NR (<50 – >
80) y |
| | >80 y: 0.05 S (MA); 0.03 S (MN) | • Psychometric properties: NR | • Race/ethnicity: White 96% (MA); 99% (MN); Black 4%
(MA); 1% (MN) |
|
| • Links: NA | • Links to outcomes: NR | • Case characteristics: women > 60 y; stage I–II
BC |
| • % appropriate use of axillary lymph node
dissectionIV
| • Overall: 81% (MA); 94% (MN) | • Funding source: NR | • Socioeconomic status: income <$40,000 54%(MA);
67% (MN); urban 95% |
| | • by age (OR) | • State of use: NR | • Funding: NCI grants |
| | 50–59 y: 0.8 NS (MA); 5.3 NS (MN) | • Current use: external quality oversight;
research | |
| | 60–69 y: 0.3 NS (MA); 0.9 NS (MN) | • Care setting: hospitals; cancer centers; RT
centers | |
| | 70–79 y: 0.1 S (MA); 0.2 S (MN) | • Professionals: clinicians; oncologists; surgeons; RT
oncologists | |
| | >80 y: 0.03 S (MA); 0.1S (MN) | | |
|
| • Links: NA | | |
| • % appropriate use of CT*IV
| • Overall: 97% (MA); 94% (MN) | | |
|
| • Links: NA | | |
| • % appropriate use of tamoxifenIV
| • Overall: 63% (MA); 59% (MN) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; CT =
chemotherapy; RT = radiotherapy; HT = hormone therapy; ER = estrogen
receptor; PR = progesterone receptor; CPG = clinical practice
guidelines; DCIS = ductal carcinoma in situ; BC = breast cancer; NCI
= National Cancer Institute; MA = Massachusetts; MN = Minnesota; OR
= odds ratio; state of use = last 3 y; GP = general practitioner; *
premenopausal; node (+); ** postmenopausal nodes (+) & ER
(+); BCS = breast-conserving surgery; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Guadagnoli, 1998b, US |
Process:
| • Overall: 74%(MA); 48% (MN) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: convenience sample women BC stage I or II
in hospitals of 2 US states (MA & MN), 1993-1995 |
| • % appropriate use of BCSIV
| • by age (OR): | • Data sources: medical records; patient survey | • Exclusion: bilateral disease; prior BCS in same
breast; prior RT; pregnancy; central tumor; multifocal; etc |
| | 50–59 y: 0.9 NS (MA); 0.9 NS (MN) | • Developmental period: NR | • Period: 2 y (1993-1995) |
| | 60–69 y: 0.9 NS (MA); 0.7 NS (MN) | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): MA: 1,514/1,299; MN:
1,061/836 |
| | 70–79 y: 0.6 NS (MA); 0.6 S (MN) | • Data sources: NR | • Age (mean & range): NR
(<50–>80) y |
| | ≥80 y: 0.8 NS (MA); 0.4 S (MN) | • Psychometric properties: NR | • Race: White (96%); Black (4%) |
| | • by residence: | • Links to outcomes: NR | • Case characteristics: mostly women > 60 y,
stage I disease |
| | Urban: 1.5 NS (MA); 2.2 S (MN) | • Funding source: NR | • Socioeconomic status: income < U$ 40,000 (MA:
55%; MN: 67%); urban (MA: 95%; MN: 91%); comorbid disease (MA: 63%;
MN: 67%) |
| | • by income (OR): | • State of use: NR | • Funding: NCI |
| | <$40,000: 0.7 NS (MA); 1.4 NS (MN) | • Current use: external quality oversight | |
| | By HMO member: 1.4 NS (MA); 0.9 NS (MN) | • Care setting: hospitals; cancer centers; RT
centers | |
| | • by education (% High school) (OR): | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
| | 70–79: 0.9 NS (MA); 1.5 NS (MN) | | |
| | 80–89: 0.9 NS (MA); 1.4 NS (MN) | | |
| | ≥90: 1.4 NS (MA); 2.6 NS (MN) | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCSIV
| • Overall: 84% (MA); 86% (MN) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; RT =
radiotherapy; NCI = National Cancer Institute; MA = Massachusetts;
MN = Minnesota; NIH = National Institute of Health; state of use =
last 3 y; GP = general practitioner; OR = odds ratio; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Haas, 2000, US |
Process:
| • Overall: 69.1% | • Standard: Harvard Risk Management Foundation
guidelines, 1995 | • Inclusion: convenience sample women referred for at
least 1 visit to GP, 1 y prior to Mx; abnormal screening Mx or
underwent Mx for clinical breast concern (lump, thickening, breast
pain) regardless of result, Greater Boston area |
| • % appropriate use of evaluation in compliance with
guidelines (biopsy; imaging evaluation; breast exam)IV
| • by consultation: | • Data sources: medical records; baseline &
follow-up telephone surveys | • Exclusion: previously diagnosed BC; evaluated for
abnormal Mx or breast complaint within preceding y |
| | Abnormal Mx: 74% | • Developmental period: NR | • Period: 1 y (1996 -1997) |
| | Clinical breast complaint: 58.8% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 751/579 |
| | • by age: | • Data sources: NR | • Age (mean & range): NR |
| | <50 y: 63.8% | • Psychometric properties: NR | • Race/ethnicity: White (74.4%); Black (14.5%);
Hispanic (5.7%) |
| | ≥50 y: 74.5 % | • Links to outcomes: NR | • Case characteristics: NR |
| | • by race/ethnicity: | • Funding source: NR | • Socioeconomic status: ≥ high school (50%); HMO
(60%) |
| | White: 71% | • State of use: NR | • Funding: Harvard Risk Management Foundation |
| | Black: 59.5% | • Current use: internal quality improvement | |
| | Hispanic: 75.8% | • Care setting: hospitals; cancer centers | |
| | • by payer: | • Professionals: GPs; oncologists; surgeons | |
| | HMO: 73.3% | | |
| | other: 62% | | |
|
| • Links: NA | | |
|
Outcome:
| • Overall: excellent care 46.8% (baseline) | | |
| • % women reporting overall satisfaction with quality
of breast careIV
| 45.8% (follow-up survey) | | |
| | • by age: | | |
| | <50 y: 44.4% (b)- 46.6%(F) | | |
| | ≥ 50 y: 49.3% (b)- 44.9% (F) | | |
| | • by Race/ethnicity: | | |
| | White: 51.9% (b)- 49.8% (F) | | |
| | Black: 35.9% (b)- 35.6% (F) | | |
| | Hispanic: 33.3% (b)-25% (F) | | |
| | • by payer: | | |
| | HMO: 42.9% (b) - 42.4% (F) | | |
| | other: 52.8% (b) – 50.7% (F) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; Mx = mammogram; state of use = last 3 y; GP = general
practitioner; HMO = health maintenance organization; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Harlan, 2002, US |
Process:
| • Overall: 70% | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: population-based sample women stage I, II
& IIIA BC diagnosed, 1987-1991 & 1995 |
| • % appropriate use of any adjuvant systemic therapy in
node (+)IV
| • by age | • Data sources: NCI- SEER cancer registries | • Exclusion: pts who did not undergo surgery;
participation in clinical trials |
| | <51y: 82% | • Developmental period: NR | • Period: 5 y (1987-1991 & 1995) |
| | 51–64 y: 73% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 8,106/7,724 |
| | ≥65 y: 63% S | • Data sources: NR | • Age (mean & range): NR |
| | • by race/ethnicity: | • Psychometric properties: NR | • Race/ethnicity: White (83.2%); Black (9.3%); other
(7.5%) |
| | White: 72% | • Links to outcomes: NR | • Case characteristics: women stage I–IIIA BC; ER (+)
(59.2%); tumor size 1–2 cm (47.7%); node (-) (63.4%) |
| | Black: 69% | • Funding source: NR | • Socioeconomic status: NR |
| | other: 72% NS | • State of use: NR | • Funding: NCI |
|
| • Links: NA | • Current use: external quality oversight;
research | |
| • % appropriate use of any adjuvant systemic therapy in
node (-)IV
| • Overall: NR | • Care setting: hospitals; cancer centers | |
| | • by age: | • Professionals: oncologists; GPs | |
| | <51 y: 45% | | |
| | <65 y: 46% | | |
| | ≥65 y: 41% | | |
| | • by race/ethnicity: | | |
| | White: 44% | | |
| | Black: 40% | | |
| | other 45% NS | | |
|
| • Links: NA | | |
| • % appropriate decision not to provide adjuvant
systemic therapy in node(-); tumor <1cmIV
| • Overall: 52.2% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; node (+) = lymph node positive; node (-) = lymph node
negative; NIH = National Health Institute; NCI SEER = National
Cancer Institute Surveillance, Epidemiology, and End-Results; state
of use = last 3 y; GP = general practitioner; Level Ia = pre-study
data indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Hassey Dow, 2000, US |
Outcome:
| • Overall: NR; NS changes over time in QLI scales | • Instrument(s): Ferrans Quality-of-Life Index- cancer
version (QLI) 1990 | • Inclusion: convenience sample women ESBC beginning
course of RT after BCS at a major urban teaching hospital in US
Northeast. 21–45 y; newly diagnosed stage I or II BC; not undergoing
CT or HT |
| • % women reporting changes in QOL overtime (from start
of RT; during RT & 6 mo post)Ia
| • Links: NA | • Data sources: questionnaires; demographic data
form | • Exclusion: no previous diagnosis or treatment for any
cancer |
| | | • Developmental period: NR | • Period: 6 mo |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 28/23 |
| | | • Data sources: NR | • Age (mean & range): 37.8 (25–45) y |
| | | • Psychometric properties: NR | • Race/ ethnicity: White (91%); Hispanic &
Russian (4%) |
| | | • Links to outcomes: NR | • Case characteristics: women BC stage I or II; BCS
& RT; <45 y |
| | | • Funding source: NR | • Socioeconomic status: single (40%) |
| | | • State of use: NR | • Funding: ONS Foundation/Laderle Research |
| | | • Current use: external quality oversight;
research | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; RT =
radiotherapy; CT = chemotherapy; HT = hormone therapy; QOL = quality
of life; QLI = Ferrans Quality-of-Life Index - Cancer version; state
of use = last 3 y; GP = general practitioner; Level Ia = pre-study
data indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Hebert-Croteau, 1999,
Canada |
Process:
| • Overall: NR | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: random sample newly diagnosed stage I–II
BC women ≥50 y receiving treatment in 5 sanitary regions of Quebec:
Montreal, Quebec, Laval, Monteregie &
Chadiere/Appalaches |
| • % appropriate use of definitive locoregional therapy
(total mastectomy + ALND or BCS + ALND + RT) IV
| • by age: | • Data sources: Quebec tumor registry (1988-89); Quebec
hospital admission/discharge database (1993-1994) | • Exclusion: pts in long term or convalescent
hospitals; diagnostic errors; multiple primary tumors; recurrent BC;
regional or distant extension; multicentric, inflammatory, Stage
III–IV; no pathological confirmation of disease; tumor not
originated in mammary gland; phyllodes tumor or lobular
carcinoma |
| | 50–69 y: 83.5% | • Developmental period: NR | • Period: 2 y (1993-1994) |
| | ≥70 y: 48.7% S | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 1,732/1,174 |
|
| • Links: NA | • Data sources: NR | • Age (mean & range): NR (50–>70) y |
| • % appropriate use of alternative definitive therapy
(RT after BCS + ALND or adjuvant treatment)IV
| • Overall: NR | • Psychometric properties: NR | • Race/ethnicity: NR |
| | • by age: | • Links to outcomes: NR | • Case characteristics: Stage I–II BC node (-); ER (+)
(70–79%); tumor size 1–2 cm (41–48%) |
| | 50–69 y: 90.9% | • Funding source: NR | • Socioeconomic status: NR |
| | ≥70 y: 60.9% S | • State of use: NR | • Funding: Research in Health Quebec |
|
| • Links: NA | • Current use: research; external quality
oversight | |
| • % appropriate of use of BCSIV
| • Overall: NR | • Care setting: hospitals; cancer centers | |
| | • by age: | • Professionals: oncologists; GPs; RT oncologists;
surgeons | |
| | 50–69 y: 90.9% | | |
| | ≥70 y: 80.1% S | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCSIV
| • Overall: NR | | |
| | • by age: | | |
| | 50–69 y: 89.6% | | |
| | ≥70 y: 59% S | | |
|
| • Links: NA | | |
| • % appropriate use of ALNDIV
| • Overall: NR | | |
| | • by age: | | |
| | 50–69 y: 82.4% | | |
| | ≥70 y: 46.9% S | | |
|
| • Links: NA | | |
| • % appropriate use of any adjuvant systemic
therapyIV
| • Overall: NR | | |
| | • by age: | | |
| | 50–69 y: 74.2% | | |
| | ≥70 y: 72.1% NS | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; LN = lymph nodes; LND = lymph node
dissection; ALND = axillary lymph node dissection; RT =
radiotherapy; enrolled = n qualified; evaluated = n analyzed;
completed = n completing the study; GP = general practitioner; state
of use = last 3 y; BCS = breast -conserving surgery; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Hislop, 2003, Canada |
Process:
| • Overall: NR | • Standard: BCCA cancer treatment policy manual,
1995 | • Inclusion: Population-based sample women
histologically confirmed BC diagnosed, British Columbia, 1995 |
| • % appropriate use of BCSIV
| • by extent of disease: | • Data sources: British Columbia cancer registry;
medical records; interviews of MDs | • Exclusion: diagnosed out of province; at death;
previous synchronous cancer |
| | LCIS: 56% | • Developmental period: NR | • Period: 1 y (1995) |
| | DCIS: 39% | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 2,563/1,159 |
| | Metastatic: 8% | • Data sources: NR | • Age (mean & range): NR |
| | M0 invasive: 57% | • Psychometric properties: NR | • Race/ethnicity: NR |
| | Node (-): 60% | • Links to outcomes: NR | • Case characteristics: DCIS or LCIS (n = 152);
invasive non metastatic (n = 967); node (-) (n = 496); metastatic (n
= 40) |
| | • By age: | • Funding source: NR | • Socioeconomic status: NR |
| | <40 y: 42% | • State of use: NR | • Funding: British Columbia Health Research |
| | 40–49 y: 51% | • Current use: external quality oversight | |
| | 50–59 y: 58% | • Care setting: hospitals; cancer centers; RT
centers | |
| | 60–69 y: 50% | • Professionals: oncologists; surgeons; RT oncologists;
GPs | |
| | 70–79 y: 42% | | |
| | • > 80 y: 41% | | |
| | • by family income: | | |
| | <$35,000: 44% | | |
| | $35,000–44,999: 46% | | |
| | $45,000–54,999: 46% | | |
| | ≥$55,000: 55% | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCS + ALND in M0
invasive BCIV
| • Overall: 38% | | |
| | • by family income: | | |
| | <$35,000: 100% | | |
| | $35,000–44,999: 80% | | |
| | $45,000–54,999: 89% | | |
| | ≥$55,000: 82% | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCS in
DCISIV
| • Overall: 38% | | |
|
| • Links: NA | | |
| • % appropriate use of mastectomy ± RT + ALDN in M0
invasiveIV
| • Overall: 46% | | |
|
| • Links: NA | | |
| • % appropriate use of mastectomy ± RT in LCIS or
DCISIV
| • Overall: 21% | | |
|
| • Links: NA | | |
| • % no BCS or mastectomy in metastatic
diseaseIV
| • Overall: 65% | | |
|
| • Links: NA | | |
| • % appropriate use of treatment sequences according to
guidelinesIV
| • Overall: 81% | | |
| | • By extent of disease: | | |
| | LCIS: 78% | | |
| | DCIS: 71% | | |
| | Metastatic: 73% | | |
| | M0 invasive: 83% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; state of use = last 3 y; GP = general practitioner;
BCCA = British Columbia Cancer Agency; DCIS = ductal carcinoma in
situ; LCIS = lobular carcinoma in situ; BCS = breast-conserving
surgery; RT = radiotherapy; ALND = axillary lymph node dissection;
M0 = non-metastatic; MD = medical doctor; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Imperato, 2002, US |
Process:
| • Overall: 99.3% (551/555) | • Standard: CAP & ADASP guidelines 1997/2000
(update) | • Inclusion: random sample Medicare Individuals BC who
underwent total mastectomy with LND, NY State hospitals, 1999 |
| • % reporting laterality of
specimen (right or left breast)IV
| • Links: NA | • Data sources: Medicare pts, NY State acute care
hospitals, 1999 (n=1,718); medical records | • Exclusion: other type of surgery, missing data from
records, no residual cancer present in individuals with prior
lumpectomy or excisional biopsy |
| • % reporting gross observation of lesionIV
| • Overall: 60.5% (336/555) | • Developmental period: NR | • Period: 1 y (1999) |
|
| • Links: NA | • Reference standard(s) (Publication date): NR | • n patients (enrolled/ evaluated): 1718/555* |
| • % reporting dimension of tumor (largest)IV
| • Overall: 93.5% (314/336)\ | • Data sources: NR | • Age (mean & range): 73.7 (NR) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: White (80.9%); Black (8.5%) Asian
(1.1%); unknown (9.5%) |
| • % reporting identification of affected
quadrantIV
| • Overall: 30.7% (103/336) | • Links to outcomes: NR | • Case characteristics: NR |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % reporting LN (presence/absence)IV
| • Overall: 83.7% (465/555) | • State of use: NR | • Funding: Health Care Financing Administration |
|
| • Links: NA | • Current use: external quality oversight; quality of
care reporting | |
| • % reporting presence of carcinomaIV
| • Overall: 100% (555/555) | • Care setting: hospitals; pathology centers | |
|
| • Links: NA | • Professionals: pathologists; oncologists;
surgeons | |
| • % reporting histological typeIV
| • Overall: 95.9% (532/555) | | |
|
| • Links: NA | | |
| • % reporting histological gradeIV
| • Overall: 59.1% (328/555) | | |
|
| • Links: NA | | |
| • % reporting nuclear gradeIV
| • Overall: 44.3% (246/555) | | |
|
| • Links: NA | | |
| • % reporting mitotic rateIV
| • Overall: 22.5% (125/555) | | |
|
| • Links: NA | | |
| • % reporting extent of tubule formationIV
| • Overall: 19.6% (109/555) | | |
|
| • Links: NA | | |
| • % reporting verification tumor sizeIV
| • Overall: 63.0% (349/555) | | |
|
| • Links: NA | | |
| • % reporting angiolymphatic invasionIV
| • Overall: 45.6% (253/555) | | |
|
| • Links: NA | | |
| • % reporting resection margin statusIV
| • Overall: 69.4% (385/555) | | |
|
| • Links: NA | | |
| • % reporting n LN presentIV
| • Overall: 93.5% (519/555) | | |
|
| • Links: NA | | |
| • % reporting n node (+)IV
| • Overall: 98.6% (217/220) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; LN = lymph
nodes; LND = lymph node dissection; (+) = positive; CAP = College of
American Pathology; ADASP = Association of Directors of Anatomic and
Surgical Pathology; state of use = last 3 y; NY = New York; Level Ia
= pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Jackson, 1999,
Canada |
Process:
| • Overall: 82.5% (4%–95.5%) | • Standard: BCCA guidelines, 1986, update in 1989
& 1993 | • Inclusion: population-based sample women receiving
“radical” or “adjuvant” postoperative RT treatments for BC in 3
clinics in British Columbia inclusive, 1985-1996 |
| • % appropriate use of RT
post-mastectomy on chest wallIV
| • Links: NA | • Data sources: CAIS, Radiation Therapy Warehouse
Table | • Exclusion: pts receiving palliative treatment or
treatment for other disease sites; referrals to other hospitals |
| • % appropriate use of RT on regional LNIV
| • Overall: 75% (3%–92%) | • Developmental period: NR | • Period: 12 y (1985-1996) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 9,748/9,351 |
| • % quality of RT after BCSIV
| • Overall: 95% (69%–99.5%) | • Data sources: NR | • Age (mean & range): NR |
| | • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: NR |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: NR |
| | | • Current use: external quality oversight | |
| | | • Care setting: hospitals; cancer certers; RT
oncologists; | |
| | | • Professionals: RT oncologists; oncologists; surgeons;
GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; RT = radiotherapy; CAIS = Cancer Agency Information
System; LN = lymph nodes; BCS = breast-conserving surgery; state of
use = last 3 y; GP = general practitioner BCCA = British Columbia
Cancer Agency; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Jansen, 2000,
Netherlands |
Outcome:
| • Overall: QOL scale: 38% (worse); 40% (stable); 22%
(improvement) | • Instrument(s): Rotterdam Symptom Checklist (RSCL);
SF-36 | • Inclusion: convenience sample women ESBC who
underwent surgery (BCS or mastectomy) |
| • Overall changes in QOL overtime; before &
after RTIac
| • Links: NA | • Data sources: pt self-report questionnaires before RT
(pretest); after RT (post-test) & recall of pretest | • Exclusion: previous CT or RT; DCIS; no speak
Dutch |
| | | • Developmental period: NR | • Period: 2 y (1997-1999) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 76/46 |
| | | • Data sources: NR | • Age (mean & range): 55 (28–77) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: women BC stage I or II; BCS
(n=37); mastectomy (n=9) |
| | | • Funding source: NR | • Socioeconomic status: married (72%); full-time
employment (17%) |
| | | • State of use: NR | • Funding: Dutch Cancer Society |
| | | • Current use: external quality oversight;
research | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC:
early stage breast cancer; BCS: breast-conserving surgery; RT:
radiotherapy; CT: chemotherapy; QOL: Quality of life; DCIS: ductal
in situ carcinoma; state of use: last 3 y; GP = general
practitioner; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Keating, 2001, US |
Process:
| • Overall: 73.8% (MA); 48% (MN) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: convenience sample women diagnosed stage I
& II BC at 17 hospitals in MA & 30 hospitals in
MN |
| • % appropriate use of
BCSIV
| • Links: NA | • Data sources: medical records; telephone interview
with pts | • Exclusion: women BC DCIS; bilateral synchronous
carcinoma; inflammatory carcinoma; women interview non-responders
(no permission by surgeon, not located, unavailable) |
|
Outcome:
| • Overall: Very satisfied: | • Developmental period: NR | • Period: 2 y (1993-1995) |
| • % satisfaction of women with treatment choice after
discussing with oncologist or surgeonIV
| 80% (MA); 76% (MN) | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 1,498/792 (MA);
2,330/1,634 (MN) |
|
| • Links: NA | • Data sources: NR | • Age (mean & range): 56.6 y (SD 13.5) MA; 59.4
y (SD 13.6) MN |
| • % participation of women with BC in decision-making
as much as they wantedIV
| • Overall: 83% (MA); 81% (MN) | • Psychometric properties: NR | • Race/ethnicity: White 94% (MA); 98% (MN) S |
|
| • Links: NA | • Links to outcomes: NR | • Case characteristics: women BC stage I 58% MA; 60%
MN; stage II 42% MA; 40% MN |
| • % received enough information about surgery &
RTIV
| • Overall: 80% (MA); 80% (MN) appropriate | • Funding source: NR | • Socioeconomic status: income < U$20,000/y: 17%
MA; 22% MN; U$20,000–40,000/y: 29% MA; 34% MN; >U$40,000/y:
54% MA; 44% MN (p<0.05); HMO insurance 33% MA; 43% MN
(p<0.05) |
| | • Links: NA | • State of use: NR | • Funding: NCI; Doris Duke Charitable Foundation |
| | | • Current use: external quality oversight | |
| | | • Care setting: hospitals; pathology centers | |
| | | • Professionals: pathologists; oncologists;
surgeons | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; MA = Massachusetts; MN = Minnesota LN = lymph nodes; BCS =
breast-conserving surgery; RT = radiotherapy; n = number; HR =
hormone receptor; DCIS = ductal carcinoma in situ; BC = breast
cancer; NIH = National Institute of Health; state of use = last 3 y;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Khawaja, 2001, UK |
Access:
| • Overall: 100% (22/22) | • Standard: BASO breast group recommendations 1995/1998
(update) | • Inclusion: convenience sample women BC referred by GP
to specialist to diagnose: breast lump; suspicion of malignant
change; other breast symptoms |
| • % women BC to be seen by specialist within 2 wks of
referral (standard: ≥80%) for diagnostic purposesIV
| • Soon (<10 d): | • Data sources: referrals faxed to breast clinic | • Exclusion: benign disease |
| | >65 y: 18.2% (4/22) | • Developmental period: NR | • Period: 3 mo (1998) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 100/22 |
| • % urgent referrals seen within 5 working d (standard:
≥80%)IV
| • Overall: 82% | • Data sources: NR | • Age (mean & range): 50 (22–90) y |
| | • by age: | • Psychometric properties: NR | • Race/ethnicity: NR |
| | 41–65 y: 27.3% (6/22) | • Links to outcomes: NR | • Case characteristics: NR |
| | >65 y: 54.5% (12/22) | • Funding source: NR | • Socioeconomic status: NR |
| | • Links: NA | • State of use: NR | • Funding: NR |
| | | • Current use: research; internal quality improvement;
external quality oversight | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: GPs; oncologists; surgeons | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC: breast
cancer; BASO: British Association of Surgical Oncology; state of
use: last 3 y; GP = general practitioner; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Lagorreta, 2000, US |
Process:
| • Overall: 63% (474/748) | • Standard: NIH Consensus Conference recommendations,
1990 | • Inclusion: convenience sample women ≥ 21 y ESBC
detected, 1994-1996, with invasive carcinoma (any histological
subtype); DCIS; stages 0–II; primary tumor ≤ 5 cm; no evidence
multicentricity of tumor; no CI to RT; Paget's disease of breast;
eligible for BCS |
| • % appropriate use of BCS when indicatedIV
| • by stage: Stage 0 & I were 16% (OR: 1.16;
S)& 21 % (OR: 1.21; S) respectively, more likely to receive
BCS vs stage II pts | • Data sources: claims data of Health Net (~1.3 million
member); HMO of California; medical records | • Exclusion: lobular carcinoma in situ; phyllodes
tumor, or sarcoma; primary tumor > 5 cm &/or stage
III or IV |
| | • by race/ethnicity: | • Developmental period: NR | • Period: 2 y (1994-1996) |
| | Hispanic women 36% less likely to receive BCS vs White
women (OR: 0.36; S) | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 1,017/753 |
| | By Marital Status (OR): | • Data sources: NR | • Age (mean & range): NR (≤ 39– ≥ 65) y |
| | Married: 0.93 | • Psychometric properties: NR | • Race/ethnicity: White (72.6%); Hispanic (6.8%); Black
(5.2%); unknown (8.5%) |
| | Not married/widowed: 1.00 | • Links to outcomes: NR | • Case characteristics: ESBC stage 0 (8.2%); I (50.1%;
II (41.7%), tumor size 1.1–2 cm (45.3%) |
| | • Links: NA | • Funding source: NR | • Socioeconomic status: Married (61.8%) |
| | | • State of use: current | • Funding: NR |
| | | • Current use: external quality oversight | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: oncologists; surgeons; GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BCS =
breast-conserving surgery; CI = contraindication; CT = chemotherapy;
NIH =National Health Institute; ESBC = early stage breast cancer;
DCIS = ductal carcinoma in situ; RT = radiotherapy; OR = odds ratio;
HMO = Health Maintenance Organization; state of use = last 3 y; GP =
general practitioner; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Lazovich, 1997, US |
Process:
| • Overall: NR | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: national population-based sample women
ESBC stage I or II diagnosed in 13 western, Washington counties,
1983-1993 |
| • % appropriate use of BCSIV
| • by stage: | • Data sources: SEER cancer registries; medical
records | • Exclusion: locally advanced BC; distant metastases;
no measurable breast mass; data missing |
| | Stage I: 54.9% | • Developmental period: NR | • Period: 3 y (1990-1993) |
| | Stage II: 35.2% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 18,664/13,541 |
| | • by age: | • Data sources: NR | • Age (mean & range): NR |
| | <50 y: 52.1% | • Psychometric properties: NR | • Race/ethnicity: NR |
| | 50–59 y: 54.9% | • Links to outcomes: NR | • Case characteristics: women BC stage I or II;
<5 cm |
| | 60–69 y: 47.4% | • Funding source: NR | • Socioeconomic status: NR |
| | 70–79 y: 39.1% | • State of use: NR | • Funding: NCI |
| | > 80 y: 31.7% S | • Current use: external quality oversight;
research | |
| | • by payer: | • Care setting: hospitals; cancer centers; RT
centers | |
| | Private: 46.2% | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
| | HMO: 69.9% S | | |
| | • by education: | | |
| | Lowest tertile: 44.9% | | |
| | Middle tertile: 49.9% | | |
| | Highest tertile: 50.9% S | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCSIV
| • Overall: 94.1% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; RT =
radiotherapy; NIH = National Institute of Health; SEER =
Surveillance, Epidemiology and End Results; NCI = National Cancer
Institute; state of use = last 3 y; GP = general practitioner; Level
Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Lazovich, 1999, US |
Process:
| • Overall: NR | • Standard: NIH Consensus Conference recommendations,
1990 | • Inclusion: national population-based sample women
ESBC diagnosed in 9 US regions, 1983-1995 |
| • % appropriate use of BCSIV
| • by stage: | • Data sources: SEER cancer registries (9 US
regions) | • Exclusion: DCIS; Paget's disease; non measurable
tumor; tumor > 5 cm; stages III or IV; data missing |
| | Stage I: 53.4%(29,234/55,984) | • Developmental period: NR | • Period: 5 y (1990-1995) |
| | Stage II: 32.7%(22,746/53,896) | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 110,235/109,880 |
| | • by age: | • Data sources: NR | • Age (mean & range): NR |
| | <50 y: 48% | • Psychometric properties: NR | • Race/ethnicity: White, non-white |
| | 50–59 y: 49% | • Links to outcomes: NR | • Case characteristics: women BC stage I or II;
<5 cm |
| | 60–69 y: 44.6% | • Funding source: NR | • Socioeconomic status: NR |
| | 70–79 y: 39.2% | • State of use: NR | • Funding: NIH |
| | ≥ 80 y: 34.7% | • Current use: external quality oversight;
research | |
| | • by Race/ethnicity: | • Care setting: hospitals; cancer centers; RT
centers | |
| | White: 44.5% | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
| | Non-White: 43.1% | | |
| | • Per Registry: | | |
| | lowa; 26.7% | | |
| | Atlanta:42.1% | | |
| | Utah: 35% | | |
| | New Mexico: 40.1% | | |
| | Hawaii: 46.9% | | |
| | Detroit: 41.2% | | |
| | Connecticut: 55.6% | | |
| | SanFranscisco/Oakland: 50.8% | | |
| | Seattle/Puget Sound: 50% | | | |
|
| • Links: NA | | |
| • % appropriate use RT after BCSIV
| • Overall: 81.5% (23,042/37,196) | | |
| | • by Stage: | | |
| | Stage I: 83.5% | | |
| | Stage II: 77.4% S | | |
| | • by Age: | | |
| | <50 y: 82.4% | | |
| | 50–59 y: 86.1% | | |
| | 60–69 y: 86.6% | | |
| | 70–79 y: 80.2% | | |
| | ≥80 y: 48.5% S | | |
| | • by Race/ethnicity: | | |
| | White: 81.7% | | |
| | Non-White: 80.7% NS | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BCS =
breast-conserving surgery; RT = radiotherapy; NIH = National
Institute of Health; SEER = surveillance, epidemiology and end
results; state of use = last 3 y; GP = general practitioner; Level
Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Mandelblatt, 2001,
US, |
Process: | • Overall: 35.5% | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: national random sample, Medicare
beneficiaries, ≥ 67 y, newly diagnosed ESBC, 1992-1994; surgeons
treating above mentioned group of pts |
| • % appropriate use of BCSIV
| • by surgeon profile: | • Data sources: claims data from FFS Medicare sector;
surveys sent to treating surgeons; telephone surveys with
surgeons | • Exclusion: women ≥ 67 y Stage I, IIA, or IIB BC;
bilateral BC; multicentricity of cancer |
| | surgeons with BCS propensity: 44.4% | • Developmental period: NR | • Period: 6 y (1992-1998) |
| | surgeons with mastectomy propensity: 26.8% S | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 3,851/3,851 |
|
| • Links: NA | • Data sources: NR | • n surgeons (enrolled/evaluated): 1,531/1,000 |
| • % appropriate use of RT after BCSIV
| • Overall: 72.1% | • Psychometric properties: NR | • Age (mean & range): NR |
| | By surgeon profile: | • Links to outcomes: NR | • Race/ethnicity: NR |
| | surgeons with BCS+ RT propensity: 75.1% | • Funding source: NR | • Case characteristics: NR |
| | surgeons with no RT propensity: 63.2% S | • State of use: NR | • Socioeconomic status: NR |
| | • Links: NA | • Current use: research | • Funding: grants: AHRQ & Department of the
Army grants |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: surgeons; oncologists; RT oncologists;
GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; NIH = National Institute of Health; FFS =
fee-for-service; BCS = breast-conserving surgery; RT = radiotherapy;
AHRQ = Agency for Healthcare Research and Quality; state of use =
last 3 y; GP = general practitioner; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Mandelblatt, 2002,
US |
Process:
| • Overall: 33% (599/1,833) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: national random sample, fee-for service
Medicare beneficiary women ≥67 y newly diagnosed primary,
unilateral, histologically confirmed stage I–II BC treated,
1994 |
| • % apropriate use of BCSIV
| • by race/ethnicity: | • Data sources: Medicare data; surgeon contacts;
surviving women contacts; 1990 Census File; 1993 & 1995 data
from Area Resource File | • Exclusion: previous BC; DCIS without invasive
disease; metastatic or multicentric BC; bilateral breast procedures;
women BC without surgical procedure; breast surgery not
1st procedure; BC not primary diagnosis; missing
data |
| | Black: 31% (300/984) | • Developmental period: NR | • Period: 1 y (1994) |
| | White: 35% (299/849) NS | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 6,998/1,833 |
|
| • Links: NA | • Data sources: NR | • Age (mean & range): 74.4 (68.1–80.7) y |
| • % appropriate use of RT after BCSIV
| • Overall: 66.6% (399/599) | • Psychometric properties: NR | • Race/ethnicity: Black (53.7%); White (46.3%) |
| | • by race/ethnicity: | • Links to outcomes: NR | • Case characteristics: stage I: Black (53%); White
(60%); stage IIA: Black (35%); White (33%); stage IIB: Black (12%);
White (7%) |
| | Black: 61% (183/300) | • Funding source: NR | • Socioeconomic status: women < poverty level:
Black (15.2±7.3%); White (11.8±5.8%); monthly income
<U$1,000: Black (54%); White (24%); ≥U$1,000: Black (27%);
White (56%); ≤ High school: Black (76%); White (64%); married: Black
(32%); White (46%); Medicaid: Black (25%); White (6%); private
insurance: Black (43%); White (84%) |
| | White: 72.2% (216/299) S | • State of use: NR | • Funding: AHRQ; FCCBC; Department of the Army;
& NCI grants |
|
| • Links: NA | • Current use: external quality oversight | |
| • % appropriate use of ALND after BCS or
mastectomyIV
| • Overall: 86% (1,579/1,833) | • Care setting: hospitals; cancer centers; RT
centers | |
| | • by race/ethnicity: | • Professionals: oncologists; RT oncologists; surgeons;
GPs | |
| | Black: 88% (867/984) | | |
| | White: 84% (712/849) S | | |
|
| • Links: NA | | |
| • % appropriate use of CTIV
| • Overall: 9% (172/1,833) | | |
| | • by race/ethnicity: | | |
| | Black: 11% (112/984) S | | |
| | White: 7% (60/849) | | |
|
| • Links: NA | | |
| • % appropriate use of tamoxifenIV
| • Overall: 62% | | |
| | • by race/ethnicity: | | |
| | Black: 58% (193/331) S | | |
| | White: 66% (263/401) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; DCIS = ductal carcinoma in situ; BCS =
breast-conserving surgery; RT = radiotherapy; ALND = axillary lymph
node dissection; NIH = National Institute of Health; NCI = National
Cancer Institute; AHRQ = Agency for Healthcare Research and Quality;
FCCBC = Federal Coordinating Committee on Breast Cancer; state of
use = last 3 y; GP = general practitioner; CT = chemotherapy; Level
Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
McCarthy, 1997, UK |
Access:
| • Overall: 45.5% (5/11) | • Standard: quality assurance guidelines (NHSBSP),
1994 | • Inclusion: convenience sample women operable BC
<70 y treated at Nottingham City Hospital's, 1994
Professional Unit of Surgery |
| • %(>90%) of women
requiring operation for diagnostic purposes should be admitted
within 14 d of surgical decisionIV
| • Links: NA | • Data sources: Professional Unit of Surgery's database
of Primary Breast Cancers; the Helen Garrod Breast Screening Unit's
computerized database; pathology department's computerized histology
database; individual hospital case notes | • Exclusion: NR |
| • % (90%) of women admitted for operation within 21 d
of surgical decision to operate for therapeutic
purposesIV
| • Overall: 90.4% (75/83) | • Developmental period: NR | • Period: 1 y (1994) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 251/251 |
|
Process:
| • Overall: 42.7% (32/75) | • Data sources: NR | • Age (mean & range): NR |
| • % (>90%) women BC
detected by screening should attend assessment center within 3 wks
of mammographyIV
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % (>70%) appropriate use of pre-operative
diagnosis of cancer by cytology or needle histologyIV
| • Overall: 86.7% (72/83) | • Links to outcomes: NR | • Case characteristics: NR |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % (>95%) appropriate use of first localization
biopsy operation to correctly identify impalpable
lesionsIV
| • Overall: 100% (11/11) | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: external quality oversight; research;
internal quality improvement | |
| • % (90%) appropriate use of operations carried out
with proven pre-operative diagnosis of cancer (in situ or invasive)
should not require a further operation for incomplete
excisionIV
| • Overall: 80.3% (49/61) | • Care setting: hospitals; cancer centers | |
| | • Links: NA | • Professionals: oncologists; GPs; surgeons | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; BCS = breast-conserving surgery; n =
number of participants; enrolled = n qualified; evaluated = n
analyzed; NHSBSP = national coordination group for surgeons working
in breast cancer screening; state of use = last 3 y; GP = general
practitioner; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
McGlynn, 2003, US |
Process:
| • Overall: 89.1% (n = 77) | • Standard: from observational studies and expert
opinion, to randomized controlled trials | • Inclusion: random sample women living in 12 US
metropolitan areas |
| • % (Appropriate use): If a
palpable breast mass has been detected, at least one of the
following procedures should be completed within 3 months:
fine-needle aspiration, mammography, ultrasound, biopsy and/or a
followup visitIV
| • Links: NA | • Data sources: telephone survey; medical records | • Exclusion: leaving the area; refusal to be
interviewed |
|
Process:
| • Overall: 81.6% (n = 13) | • Developmental period: NR | • Period: 2 y (1998-2000) |
| • % (Appropriate use): If a
breast mass has been detected on two separate occasions, then either
a biopsy, fine-needle aspiration or ultrasound should be performed
within 3 months of the second visitIV
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 192/192 |
|
Process:
| • Overall: 50.2% (n = 33) | • Data sources: NR | • Age (mean & range): NR |
| • % (Appropriate use): A biopsy
or fine-needle aspiration should be performed within 6 weeks either
when the mammography suggests malignancy or the persistent palpable
mass is not cystic on ultrasoundIV
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
|
Process:
| • Overall: 100% (n = 2) | • Links to outcomes: NR | • Case characteristics: NR |
| • % (Appropriate use): A biopsy
should be performed within 6 weeks if fine needle aspiration cannot
rule out malignancyIV
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
|
Process:
| • Overall: 50.2% (n = 13) | • State of use: NR | • Funding: Robert Wood Johnson Foundation |
| • % (Appropriate use): Women with
stage I or stage II breast cancer should be offered a choice of
modified radical mastectomy or breast-conserving surgery, unless
contraindications to breast-conserving surgery are
presentIV
| • Links: NA | • Current use: external quality oversight | |
|
Process:
| • Overall: 45.3% (n = 10) | • Care setting: hospitals; pathology centers | |
| • % (Appropriate use): Women
treated with breast-conserving surgery should begin radiation
therapy within 6 weeks of completing either of the following: the
last surgical procedure on the breast (including reconstructive
surgery that occurs within 6 wks of primary resection) or
chemotherapy, if patient receives adjuvant chemotherapy, unless
wound complications prevent the initiation of treatmentIV
| • Links: NA | • Professionals: oncologists; surgeons GPs; RT
oncologists | |
|
Process:
| • Overall: 85.1% (n = 13) | | |
| • % (Appropriate use): Women with
invasive breast cancer that is node-positive, or node-negative and
primary tumor ≥ 1 cm, should be treated with adjuvant systemic
therapy to include combination chemotherapy (and/or tamoxifen,
20mg/d) IV
| • Links: NA | | |
|
Process:
| • Overall: 84.6% (n = 99) | | |
| • % (Appropriate use): Women with
a history of breast cancer should have a yearly
mammographyIV
| • Links: NA | | |
|
Process:
| • Overall: 82.6% (n = 4) | | |
| • % (Appropriate use): Women with metastatic breast
cancer should be offered hormonal therapy, chemotherapy, and/or
enrollment in a clinical trial with documentation of informed
consent within 6 wks of the identification of
metastasesIV
| • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; QI = quality indicator; CI =
confidence interval; state of use = last 3 y; RT = radiotherapy; GP
= general practitioner; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Molenaar, 2001,
Netherlands |
Outcome: | • Overall: positive effect (CDROM) 0, 3 & 9 mo;
no data | • Standard: IKA/IKST: Working group on Mamma Carcinoma;
treatment guidelines; the Netherlands; Comprehensive Cancer Center,
1995 | • Inclusion: convenience sample women, newly diagnosed
stage I & II BC eligible for BCS or mastectomy |
| • % satisfaction of women BC with
treatment choiceIac
| • Links: NA | • Instrument(s): MOS20; EORTC QLQ-BR23 | • Exclusion: no Dutch spoken |
| • % change in QOL over time; generic QOL scales (higher
scores = better QOL; except for pain scores)]Iac
| • Overall: positive effect (CDROM) 0, 3 & 9 mo;
no data | • Data sources: pt self-reported questionnaires; 3
hospitals, Netherlands | • Period: 2 y (1996-1998) |
|
| • Links: NA | • Developmental period: NR | • n patients (enrolled/evaluated): 180/167 |
| • % change in QOL over time; BC- specific QOL scales
(higher scores = better functioning; except for symptoms
scales)Iac
| • Overall: positive effect (CDROM) 0, 3 & 9 mo;
no data | • Reference standard(s) (Publication Date): NR | • Age (mean & range): 55.4 (44.6–66.2) y (CDROM
group); 54.6 (44–65.2) y (standard care) |
| | • Links: NA | • Data sources: NR | • Race/ethnicity: NR |
| | | • Psychometric properties: NR | • Case characteristics: ESBC node (-) (52–57%) |
| | | • Links to outcomes: NR | • Socioeconomic status: married (53–66%); employed
(45–52%) |
| | | • Funding source: NR | • Funding: Dutch Cancer Society |
| | | • State of use: NR | |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: oncologists; surgeons; GPs; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; ESBC =
early stage breast cancer; BCS = breast-conserving surgery; QOL =
quality of life; MOS20 = medical outcomes study 20 (general health;
physical functioning; pain; role functioning; social &
psychosocial functioning); EORTC QLQ-BR23: European Organization for
Research and Treatment of Cancer Quality of Life-specific for BC pts
(body image; sexual functioning; arm symptoms; breast symptoms;
systemic therapy symptoms; & future perspective); state of
use = last 3 y; GP = general practitioner; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Mor, 1994, US
|
Outcome:
| • Overall: NR | • Instrument(s): MHI-5 | • Inclusion: convenience sample women BC from 2
research samples |
| • %change in QOL over timeIa
| • by age: | • Data sources: medical records; telephone interview
with pts | • Exclusion: NR |
| | 24–54 y: 67.6% | • Developmental period: NR | • Period: NR |
| | >55 y: 71% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 262/262 |
| | • Links: NA | • Data sources: NR | • Age (mean & range): NR (24–>55) y |
| | | • Psychometric properties: NR | • Race/ethnicity: White 92.4% |
| | | • Links to outcomes: NR | • Case characteristics: women BC; local/regional
disease; CT (80%) |
| | | • Funding source: NR | • Socioeconomic status: employed (14.3–51.8%); married
(52.9–67.7%); family income > U$ 30,000 (17.6–49.7%) |
| | | • State of use: NR | • Funding: NCI |
| | | • Current use: decision-making; research | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: oncologists; surgeons; GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; QOL = quality of life; BC = breast cancer; state of use =
last 3 y; NCI = National Cancer Institute; CT = chemotherapy; MHI-5
= Mental Health inventory (5-item scale for medically ill
population); GP = general practitioner; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Mor, 2000, US |
Process:
| • Overall: 64.1% | • Standard: NCI Consensus Conference for surgeons,
1993 | • Inclusion: random sample women > 60 y BC stage
I or II diagnosed at 6 hospitals, Providence, RI, Nov 1992 &
Feb 1997 |
| • % appropriate use of
BCSIV
| • Links: NA | • Data sources: hospital cancer registry (6 hospitals
in Rhode Island, US); pathology reports; medical records; pt
interviews | • Exclusion: women with BC <60 y; not eligible
patients for intervention (low-volume surgeons) |
| • % appropriate use of RT after BCSIV
| • Overall: 70.4 % | • Developmental period: NR | • Period: 5 y (1992-1997) |
| | • by age: | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 1,144/350 |
| | 60–69 y: 94% | • Data sources: NR | • Age (mean & range): NR (60–>80 y) |
| | 70–79 y: 83% | • Psychometric properties: NR | • Race/ethnicity: NR |
| | > 80 y: 34% S | • Links to outcomes: NR | • Case characteristics: women BC stage I, II or DCIS;
>1cm (74.9%); ER/PR known (94.7%); node (-) (38.6%), node (+)
(13.1%) |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % appropriate use of any adjuvant systemic therapy
(CT &/or HT); tumor ≥ 1 cmIV
| • Overall: 81.9% | • State of use: NR | • Funding: NCI |
| | • by age: | • Current use: internal quality improvement; external
quality oversight, research | |
| | 60–69 y: 88% | • Care setting: hospitals; cancer centers | |
| | 70–79 y: 82% | • Professionals: surgeons; oncologists | |
| | >80 y: 77% S | | |
|
| • Links: NA | | |
| • % appropriate use of treatment sequences recommended
or received (if tumor <1 cm, then mastectomy or BCS + RT. If
tumor ≥ 1 cm then mastectomy or BCS + RT & CT &/or
HT) IV
| • Overall: 72.9% | | |
| | • by age: | | |
| | 60–69 y: 89% | | |
| | >80 y: 50% S | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BCS =
breast -conserving surgery; CT = chemotherapy; RT = radiotherapy; HT
= hormone therapy; ER = estrogen receptor; PR = progesterone
receptor; CPG = clinical practice guidelines; NCI = National Cancer
Institute; state of use = last 3 y; DCIS = ductal carcinoma in situ;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Morrow, 2001, US |
Process:
| • Overall: 42.6% (7,097/16,643) | • Standard: ACOS, ACR, CAP, SSO guidelines, 1992 | • Inclusion: population-based sample women stage I–II
BC receiving diagnosis & initial course of treatment at
participating institution, 1994 |
| • % appropriate use of BCSIV
| • by age: | • Data sources: Medicare patients, NY State acute care
hospitals, 1999 (n=1,718); medical records | • Exclusion: staging not performed or incomplete; pT3
tumours; surgery other than BCS or mastectomy |
| | 21–49 y: 48.2% | • Developmental period: NR | • Period: 1 y (1994) |
| | 50–69 y: 45% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 17,931/16,643 |
| | > 70 y: 34% S | • Data sources: NR | • Age (mean & range): 60.8 (21–>70)
y |
| | • by race/ethnicity: | • Psychometric properties: NR | • Race/ethnicity: White (85.9%); Black (7.8%); Hispanic
(2.9%) |
| | White: 42.5% | • Links to outcomes: NR | • Case characteristics: clinical stage I (41.5%); stage
II (20.8%); pT1 (68%); pT2 (32%); pN0 (75.5%); pN1 (24.5%); ER (+)
(65.6%); PR (+) (56.7%); infiltrating ductal, lobular (92.6%);
postmenopausal (70.9%) |
| | Black -H: 43.7% | • Funding source: NR | • Socioeconomic status: Medicare (42.1%) |
| | • by payer: | • State of use: current | • Funding: Patterns of Care Study |
| | Government: 36.9% | • Current use: external quality oversight | |
| | Private: 48.4% S | • Care setting: hospitals; cancer centers; RT
centers | |
|
| • Links: NA | • Professionals: surgeons; RT oncologists;
oncologists | |
| • % appropriate use of RT after BCSIV
| • Overall: 86% (6,099/7,097) | | |
| | • by age: | | |
| | <70 y: 88.4% | | |
| | ≥70 y: 78.9% | | |
| | • by race/ethnicity: | | |
| | White: 86.3% | | |
| | Black -H: 83.2% | | |
| | other: 81.9% | | |
| | • by payer: | | |
| | Government: 83.3% | | |
| | Private: 88.5% S | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; enrolled = n qualified; evaluated = n
analyzed; ACOS = American College of Surgeons; ACR = American
College of Radiology; CAP = College of American Pathologists; SSO =
Society of Surgical Oncology; BCS = breast-conserving surgery; pT =
pathologic tumour size; pN = pathologic nodal status; RT =
radiotherapy; state of use = last 3 y; *BCT = tumor excision;
axillary dissection & breast irradiation for stage I
& II BC; NY = New York; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Nattinger, 2000, US |
Process:
| • Overall: 78% (1995) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: national population-based sample women
aged ≥30 y at time of first diagnosis of invasive local or regional
unilateral BC, 1983-1995 |
| • % appropriate use of definitive
locoregional therapy (total mastectomy + ALND, or BCS + ALND +
RT)IV
| • Links: NA | • Data sources: NCI SEER registry; federal ARF
information | • Exclusion: no primary BCS or mastectomy, or type of
surgery unknown; date of diagnosis unknown; delivery of RT
unknown |
| • % appropriate use of mastectomy with
ALNDIV
| • Overall: 97.3% | • Developmental period: NR | • Period: 13 y (1983-1995) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 147,432/144,759 |
| • % appropriate use of BCS with ALND &
RTIV
| • Overall: 65% | • Data sources: NR | • Age (mean & range): NR (30–>80) y |
| | • Links: NA | • Psychometric properties: NR | • Race/ethnicity: White (87.3%); Black (7.1%) |
| | | • Links to outcomes: NR | • Case characteristics: BC local (65%); regional
(35%) |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Department of Defence |
| | | • Current use: external quality oversight | |
| | | • Care setting: hospitals; cancer centers; RT
centers | |
| | | • Professionals: surgeons; oncologists; RT oncologists;
GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; enrolled = n qualified; evaluated = n
analyzed; NCI = National Cancer Institute; SEER = Surveillance,
Epidemiology, and End Results; ALDN = axillary lymph node
dissection; BCS = breast-conserving surgery; RT = radiotherapy;
state of use = last 3 y; GP = general practitioner; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Northouse, 1999, US |
Outcome:
| • Overall: QOL (FACT-B): | • Standard: BC specific version of 37-item scale
FACT-B, 1993 (physical & family well-being; relationship
with MD; emotional & functional well-being) | • Inclusion: convenience sample of black women
confirmed diagnosis of BC at least 1 mo post-diagnosis, Southeastern
region, Michigan |
| • % change in QOL after diagnosis of BC*Iac
| Mean: 116.5 (SD 20.7); (range 44–145) | • Data sources: medical oncology offices, Southeastern
region, Michigan, pts self-reported status using Questionnaire
forms | • Exclusion: pts refusal to participate in study |
| | In average: fairly high QOL scale | • Developmental period: NR | • Period: NR |
| | • by variables: | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 140/98 |
| | Node (+): lower QOL (mean: 110.8) than node (-) (mean:
120.7) | • Data sources: NR | • Age (mean & range): 55 (29–81) y |
| | Recurrence of cancer: lower QOL (mean: 107.1) vs no
recurrence (mean: 118.2) | • Psychometric properties: NR | • Race/ethnicity: Black (100%) |
| | • Links: NA | • Links to outcomes: NR | • Case characteristics: BC radical mastectomy (70%);
node (-) (57.4%) |
| | | • Funding source: NR | • Socioeconomic status: working (54.2%); retired
(38.6%); unemployed (7.2%); Income < U$15,000 29.7%); married
(41%) |
| | | • State of use: NR | • Funding: Dean's discretionary fund grant; Wayne State
University |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; | |
| | | • Professionals: oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; enrolled = n qualified; evaluated = n
analyzed; QOL = quality of life; FACT-B = functional assessment of
cancer therapy scale (version 3); state of use = last 3 y; *Higher
scores = better QOL; MD = medical doctor; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Osoba, 1999, Canada
& US |
Outcome:
| • Overall: NR | • Instrument: self-administered EORTC core QOLQ- C30
(30 items) (global score; physical; social; role functions &
fatigue in phase II & III of clinical trial) scale
0–100* | • Inclusion: convenience sample women progressive
HER-2- overexpressing metastatic BC previously treated with CT
(phase II), or who had not had previous cytotoxic CT (phase III)
received trastuzumab |
| • change in QOL in women with metastatic BC treated
with trastuzumab assessed by self-administered EORTC core QOLQ - C30
baseline & wks 12; 24; 36Ia
| By phase of study: | • Data sources: pts self-reported status using EORTC
QOL questionnaire C30 | • Exclusion: NR |
| | Phase II: no apparent worsening of scores | • Developmental period: NR | • Period: 32 wks |
| | Phase III: NS changes | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 207/154 |
| | • Links: NA | • Data sources: NR | • Age (mean & range): NR |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: women with metastatic BC with
or without previous CT |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Genentech, Inc. |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers; | |
| | | • Professionals: oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; EORTC =
European Organization for Research and Treatment of Cancer; QOL =
quality of life; QOLQ = quality of life questionnaire; state of use
= last 3 y; * Higher scores = better QOL (except in fatigue); Level
Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Ottevanger, 2002,
Netherlands |
Process:
| • Overall: 55.5% (141/254) | • Standard: Regional Guidelines (CCCE) (year: NR) | • Inclusion: population-based sample premenopausal
women, node (+) BC stages II–IIIA treated in 9 hospitals using the
guidelines, 1988-1992 |
| • % appropriate use of BCSIV
| • Links: 5-y OS | • Data sources: Regional Cancer Registry &
PALGA (Dutch National Pathology Registration System) | • Exclusion: 1 hospital opposed to CT treatment of the
CPG |
| | BCS 77% vs. mastectomy 77 % NS | • Developmental period: NR | • Period: 5 y (1993-1998) |
|
| 5-y DFS: BCS 59% vs. mastectomy
65% NS | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 254/254 |
| • % appropriate use of mastectomy in large or
multifocal tumors, tumor fixed to pectoral muscle or fascia or
skinIV
| • Overall: 44.5% (113/254) | • Data sources: NR | • Age (mean & range): NR |
| | • Links: 5-y OS | • Psychometric properties: NR | • Race/ethnicity: NR |
| | BCS 77% vs. mastectomy 77% NS | • Links to outcomes: NR | • Case characteristics: premenopausal women, node (+)
BC stages II–IIIA |
|
| 5-y DFS: BCS 59% vs. mastectomy
65% NS | • Funding source: NR | • Socioeconomic status: NR |
| • % appropriate use of RT after BCSIV
| • Overall: 100% (141/141) | • State of use: NR | • Funding: Comprehensive Cancer Centre East (CCCE) |
|
| • Links: NA | • Current use: external quality oversight; quality of
care reporting; research | |
| • % appropriate use of RT in axilla for extracapsular
extension of ALN metastasesIV
| • Overall: 84.7% (72/85) | • Care setting: hospitals; pathology centers | |
| | • Links: locoregional relapse rate: 9.4% (received) vs.
14.3% (not) NS | • Professionals: pathologists; oncologists;
surgeons | |
|
| 5-y OS: 76% (received) vs. 77%
(not) NS | | |
| • % appropriate use of parasternal RT for tumors
located medial part of breastIV
| • Overall: 49.1% (56/114) | | |
|
| • Links: NA | | |
| • % quality of CT: proper doses administered (≥85% DI
& RDI) of CMFIV
| • Overall: 78.9% (DI); 58.7% (RDI) | | |
| | • Links: 5-y OS | | |
| | <65% DI: 50% vs. >85%: 77% S | | |
|
| 5-y DFS: <65% DI: 44% vs.
>85%: 61% S | | |
| • % reporting n axillary LN investigatedIV
| • Overall: | | |
| | • by n nodes: | | |
| | ≥10: 59.2% (138/233) | | |
| | <10: 40.8% (95/233) | | |
| | • Links: 5-y OS: <10 nodes 72% vs. ≥10 nodes 81%
NS | | |
| | 5-y DFS: <10 nodes 59% vs. ≥10 nodes 64%
NS | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; LN = lymph nodes; BCS = breast -conserving surgery; RT =
radiotherapy; CPG = clinical practice guideline; ER = estrogen
receptor; PR = progesterone receptor; BC = breast cancer; ALN =
axillary lymph nodes; CMF=
cyclophosphamide/methotrexate/5-fluorouracil; CT = chemotherapy;
state of use = last 3 y; CCCE = Comprehensive Cancer Center East;
DFS = disease-free survival; OS = overall survival; Level Ia =
pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Palazzi, 2002, Italy |
Process:
| • Overall: 69% (59/85) | • Standard: SGCC, 1995 | • Inclusion: convenience sample women with prescription
of RT to breast after BCS for infiltrating carcinoma & known
ALN status |
| • % appropriate decision not to
provide adjuvant systemic therapy for women node (-), low risk
BCIV
| • Links: NA | • Data sources: database of 12 centers
participating | • Exclusion: previous or synchronous surgery for cancer
in contralateral breast |
| • % appropriate use of tamoxifen in premenopausal women
BC; node (-); intermediate riskIV
| • Overall: 33% | • Developmental period: NR | • Period: 1 y (1997) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 1,610/ 1,547 |
| • % appropriate use of tamoxifen postmenopausal women
BC; node (-); intermediate riskIV
| • Overall: 59% | • Data sources: NR | • Age (mean & range): 55 (25–82) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of CT premenopausal women BC; node
(-); high risk; ER (+)IV
| • Overall: 55% | • Links to outcomes: NR | • Case characteristics: women ESBC; premenopausal
(31%); T1 stage (81%); ER (+) (65%); node (+) (31%) |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % appropriate use of tamoxifen postmenopausal women
BC; node (-); high risk; ER (+)IV
| • Overall: 59% | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: external quality oversight;
research | |
| • % appropriate use of CT women BC node (-); high risk;
ER (-)IV
| • Overall: 59% | • Care setting: RT centers | |
|
| • Links: NA | • Professionals: RT oncologists; oncologists; surgeons;
clinicians | |
| • % appropriate use of CT premenopausal women BC node
(+); ER (-)IV
| • Overall: 90% | | |
|
| • Links: NA | | |
| • % appropriate use of CT &/or OA premenopausal
women BC node (+); ER (+)IV
| • Overall: NR | | |
| | • by treatment: | | |
| | CT: 73% | | |
| | CT+ OA: 18% | | |
| | OA: 4% | | |
|
| • Links: NA | | |
| • % appropriate use of CT postmenopausal women BC node
(+); ER (-)IV
| • Overall: 81% | | |
|
| • Links: NA | | |
| • % appropriate use of tamoxifen postmenopausal women
BC node (+);ER (+)IV
| • Overall: 40% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; SGCC = St Gallen consensus conference; RT = radiotherapy;
ESBC = early stage breast cancer; BCS = breast-conserving surgery;
ER = estrogen receptor; CT = chemotherapy, OA = ovarian ablation;
(+) = positive; (-) = negative; state of use = last 3 y; ALN =
axillary lymph node; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Perez, 2001, New Zealand
UK |
Outcome:
| • Overall: NR | • Instrument: HRQOL scale: Spitzer QLI &
uniscale questionnaire (scale 0–100); TTO | • Inclusion: Convenience sample women presenting at
Dunedin Hospital, NZ, with metastatic symptoms BC |
| • % change in QOL & TTO scales during 1 y in
metastatic disease*Iac
| • Links: NA | • Data Sources: pts self-reported status
(questionnaires) | • Exclusion: refused to complete TTO scale |
| | | • Developmental period: NR | • Period: 1 y (NR) |
| | | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 64/38 |
| | | • Data sources: NR | • Age (mean & range): 58.7 (30–80) y |
| | | • Psychometric properties: NR | • Race/ethnicity: NR |
| | | • Links to outcomes: NR | • Case characteristics: women advanced metastatic
symptomatic BC |
| | | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Cancer Society of NZ |
| | | • Current use: internal quality improvement | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; QLI =
quality of life index; BC = breast cancer; state of use = last 3 y;
HRQOL = health related quality of life; QOL = quality of life; *
Higher scores = better QOL; NZ = New Zealand; TTO = time trade-off;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Ray-Coquard, 1997,
France | • % appropriate use of treatment sequences according to
guidelines (including all medical decisions on surgery; RT; CT; HT;
initial examination & follow-up) IV
| • Overall: 54% (53/99) | • Standard: regional CPG, 1993; implemented, 1994 | • Inclusion: random sample women newly diagnosed
localized BC (DCIS to nonmetastatic invasive carcinoma) in cancer
center, Rhone Alpes area, France |
|
| • Links: NA | • Data sources: medical records | • Exclusion: concomitant health care (e.g. genetic
counselling; pain treatment; plastic surgery); early death; missing
data in records; tumor size not recorded |
| • % appropriate use of initial examinationIV
| • Overall: 86% (61/71) | • Developmental period: NR | • Period: 1 y (1995) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 701/99 |
| • % appropriate use of surgeryIV
| • Overall: 92% (91/99) | • Data sources: NR | • Age (mean & range): 51 (26–90) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of CTIV
| • Overall: 85% (84/99) | • Links to outcomes: NR | • Case characteristics: localized ESBC; node (-) 66%;
ER (+) 57%, DCIS 18% |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % appropriate use of RTIV
| • Overall: 93% (92/99) | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: internal quality improvement; external
quality oversight, decision-making; research | |
| • % appropriate use of HT (tamoxifen) IV
| • Overall: 94% (93/99) | • Care setting: hospitals; cancer centers; RT
centers | |
|
| • Links: NA | • Professionals: surgeons; oncologists; RT
oncologists | |
| • % appropriate use of follow-upIV
| • Overall: 80% (68/85) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; CT =
chemotherapy; RT = radiotherapy; HT = hormone therapy; ER = estrogen
receptor; PR = progesterone receptor; CPG = clinical practice
guidelines; DCIS = ductal carcinoma in situ; BC = breast cancer;
state of use = last 3 y; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Ray-Coquard, 2002,
France |
Process:
| • Overall: 36% | • Standard: Regional (ONCORA) CPG, 1995 | • Inclusion: random sample women newly referred
localized BC (in situ or invasive) treated in cancer network,
Rhone-Alpes Area, France, 1996 |
| • % appropriate use of treatment sequences according to
CPG (including surgery; RT; CT; HT; initial examination; follow-up)
IV
| • by intervention: | • Data sources: institutional records | • Exclusion: record with data missing (surgical
biopsy), metastases, patients refused surgery, no axillary
dissection, treatment CI |
| | Initial examination: 86% | • Developmental period: NR | • Period: 1 y (1996) |
| | Surgery: 94% | • Reference standard(s) (Publication Date): NR | • n patients (enrolled/ evaluated): 367/ 346 |
| | CT: 78% | • Data sources: NR | • Age (mean & range): 60 (30–91) y |
| | RT: 77% | • Psychometric properties: NR | • Race/ethnicity: NR |
| | HT: 79% | • Links to outcomes: NR | • Case characteristics: women localized BC, T1–T3 or In
situ, 17 mm, HR (+) 61% |
| | Follow-up: 81% | • Funding source: NR | • Socioeconomic status: NR |
| | • Links: NA | • State of use: NR | • Funding: Ministry of Health (France) |
| | | • Current use: external quality oversight | |
| | | • Care setting: hospitals; cancer centers | |
| | | • Professionals: oncologists; surgeons; GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; LN = lymph
nodes; BCS = breast-conserving surgery; RT = radiotherapy; HR =
Hormone receptor; CI = contraindication; CT = chemotherapy; HT =
hormone therapy; CPG = clinical practice guidelines; state of use =
last 3 y; GP = general practitioner; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Sauven, 2003, UK |
Process:
| • Overall: NR | • Standard: NHSBSP surgical standards, 1992 | • Inclusion: population-based sample BC women detected
by screening UK, Wales, Scotland & Northern Ireland,
1996-2001 |
| • % appropriate use of preoperative diagnosis by FNA
cytology, needle histology or biopsy (minimum: ≥70%; target
standard: ≥90%)IV
| • by y: | • Data sources: regional boundaries; KC62 Korner
returns; breast screening unit records | • Exclusion: NR |
| | 1996/97: 63% | • Developmental period: NR | • Period: 5 y (1996-2001) |
| | 1997/98: 71% | • Reference standard(s) (publication date): NR | • n patients (enrolled/ evaluated): 43,500/43,500 |
| | 1998/99: 81% | • Data sources: NR | • n surgeons (enrolled/ evaluated): 1,531/1,000 |
| | 1999/2000: 85% | • Psychometric properties: NR | • Age (mean & range): NR |
| | 2000/01: 87% | • Links to outcomes: NR | • Race/ethnicity: NR |
|
| • Links: NA | • Funding source: NR | • Case characteristics: NR |
| • % quality of technique to determine histological node
status obtained for all invasive tumors by sampling or
clearanceIV
| • Overall: NR | • State of use: NR | • Socioeconomic status: NR |
| | • by y: | • Current use: external quality oversight | • Funding: NHSBSP |
| | 1996/97: 81% | • Care setting: hospitals; cancer centers; RT
centers | |
| | 1997/98: 87% | • Professionals: surgeons; oncologists;
pathologists | |
| | 1998/99: 90% | | |
| | 1999/2000: 93% | | |
| | 2000/01: 93% | | |
|
| • Links: NA | | |
| • % quality of sampling for invasive cancer: to include
≥ 4 nodesIV
| • Overall: NR | | |
| | • by y: | | |
| | 1996/97: 89% | | |
| | 1997/98: 91% | | |
| | 1998/99: 93% | | |
| | 1999/2000: 94% | | |
| | 2000/01: 95% | | |
|
| • Links: NA | | |
|
Structure:
| • Overall: NR | | |
| • % management of cases coming to surgery from
screening program carried out by surgeons who have acquired
necessary specialist knowledgeIV
| • by y & case load: | | |
| | > 30 pts/y, high*: | | |
| | 1996/97: 63% | | |
| | 1997/98: 67% | | |
| | 1998/99: 66% | | |
| | 1999/2000: 71% | | |
| | 2000/01: 72% | | |
| | < 10 pts/y, low: | | |
| | 1996/97: 8% | | |
| | 1997/98: 7% | | |
| | 1998/99: 7% | | |
| | 1999/2000: 6% | | |
| | 2000/01: 5% | | |
|
| • Links: NA | | |
|
Access:
| • Overall: NR | | |
| • % (≥90%) women requiring an operation for diagnostic
purposes should be admitted within 14 d of surgical decision
IV
| • by y: | | |
| | 1996/97: 60% | | |
| | 1997/98: 52% | | |
| | 1998/99: 52% | | |
| | 1999/2000: 60% | | |
|
| • Links: NA | | |
| • % (≥90%) women admitted for operation within 21 d of
surgical decision to operate for therapeutic purposesIV
| • Overall: NR | | |
| | • by y: | | |
| | 1996/97: 82% | | |
| | 1997/98: 81% | | |
| | 1998/99: 80% | | |
| | 1999/2000: 77% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; NHSBSP = national health service breast screening
program; FNA = fine-needle aspiration; state of use = last 3 y;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Sawka, 1997, Canada |
Process: | • Overall: 84.9% | • Standard: Guidelines of British Columbia, 1991 | • Inclusion: population-based sample women BC node (-)
diagnosed, British Columbia, 1991 |
| • % appropriate decision not to
provide adjuvant systemic therapy in <50 y; low
riskIV
| • Links: NA | • Data Sources: Provincial Cancer Registry; medical
records; other databases (e.g. drug data) | • Exclusion: age> 90 y; diagnosis by death
certificate; death within 30 days of diagnosis; stage III or IV; in
situ disease; non-epithelial malignancies & any previous
invasive cancer or history of DCIS; node (+) or unknown nodal
status |
| • % appropriate use of CT in <50 y; high risk;
presence of LVN invasion; or tumor > 2 cm; if ER
(-)IV
| • Overall: 78.6% | • Developmental period: NR | • Period: 5 y (1993-1998) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 2,317/932 |
| • % appropriate decision not to provide adjuvant
systemic therapy in 50–65 y low riskIV
| • Overall: 90.3% | • Data sources: NR | • Age (mean & range): NR
(<50–>65) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of tamoxifen & CT or
tamoxifen in 50–65 y; high risk; ER (+)IV
| • Overall: 6.6% (tamoxifen & CT) 62.3%
(tamoxifen) | • Links to outcomes: NR | • Case characteristics: women BC node (-); tumor
<2 cm (62.1%); LVN invasion (68.8%); ER (+) (60.4%); PR (+)
(38.9%) |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: income >U$ 50,000/ y
(26.1%); rural residence (15.4%) |
| • % appropriate use of CT in 50–65 y; high risk; ER
(-)IV
| • Overall: 19.1% | • State of use: NR | • Funding: NCI of Canada (Canadian Cancer Society)
& National Health Scholar Award from Health Canada |
|
| • Links: NA | • Current use: external quality oversight | |
| • % appropriate use of adjuvant systemic therapy in
>65 y; low riskIV
| • Overall: 85.9% | • Care setting: hospitals; oncology centers; RT
centers | |
|
| • Links: NA | • Professionals: oncologists; surgeons; RT
oncologists | |
| • % appropriate use of tamoxifen in >65 y; high
risk; ER (+)IV
| • Overall: 56.5% | | |
|
| • Links: NA | | |
| • % appropriate decision not to provide adjuvant
systemic therapy in > 65 y; high risk; ER (-)IV
| • Overall: 82.1% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; LN = lymph
nodes; LVN = lymph, vessels or nerves invasion; RT= radiotherapy; ER
= estrogen receptor; PR = progesterone receptor; BC = breast cancer;
CT = chemotherapy; NCI = National Cancer Institute; DCIS = ductal
carcinoma in situ; state of use = last 3 y; Level Ia = pre-study
data indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Shank, 2000, US |
Structure:
| • Overall: 99.7% (725/727) | • Standard: ACR, ACS, CAP & SSO standards for
breast conservation treatment, 1992 | • Inclusion: random sample women stage I–II invasive BC
treated, 1993-1994 |
| • % pathology reports on
chartIV
| • Links: NA | • Data sources: survey; medical records | • Exclusion: pts not treated 1993-1994; males; purely
non-invasive carcinoma; not stage I–II BC; gross multicentric
disease; bilateral lesion; prior or concurrent malignancies;
mastectomy as primary treatment |
|
Process:
| • Overall: 91.5% (665/727) | • Developmental period: NR | • Period: 2 y (1995-1996) |
| • % appropriate use of
preoperative mammographic evaluation (performed ≤3 mo) IV
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 993/727 |
| • % reporting identification of affected
quadrantIV
| • Overall: 97.8% (711/727) | • Data sources: NR | • Age (mean & range): NR (20–>80) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: White (84.2%); Black (7.3%); Hispanic
(4.4%); Asian (2.8%) |
| • % reporting clinical size of primary
tumorIV
| • Overall: 45.9% (334/727) | • Links to outcomes: NR | • Case characteristics: age >50 y (70%); stage I
or II invasive BC; postmenopausal (68.6%) |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % reporting final gross surgical marginsIV
| • Overall: 96.8% (704/727) | • State of use: NR | • Funding: NCI |
|
| • Links: NA | • Current use: quality of care reporting; internal
quality improvement | |
| • % reporting final microscopic surgical
marginsIV
| • Overall: 95.6% (695/727) | • Care setting: hospitals; cancer centers; pathology
centers | |
|
| • Links: NA | • Professionals: RT oncologists, surgeons;
pathologists; oncologists | |
| • % reporting histopathological type | • Overall: 99.7% (725/727) | | |
|
| • Links: NA | | |
| • % reporting intraductal carcinoma
quantificationIV
| • Overall: 8.5% (62/727) | | |
|
| • Links: NA | | |
| • % reporting of extent of primary tumorIV
| • Overall: 99.3% (722/727) | | |
|
| • Links: NA | | |
| • % reporting size of invasive componentIV
| • Overall: 8.5% (62/727) | | |
|
| • Links: NA | | |
| • % reporting total pathological tumour
sizeIV
| • Overall: 95.3% (693/727) | | |
|
| • Links: NA | | |
| • % reporting ER statusIV
| • Overall: 89% (647/727) | | |
|
| • Links: NA | | |
| • % reporting PR statusIV
| • Overall: 86.4% (628/727) | | |
|
| • Links: NA | | |
| • % reporting performing flow cytometry IV
| • Overall: 95.3% (693/727) | | |
|
| • Links: NA | | |
| • % reporting cytometry ploidityIV
| • Overall: 98.9% (719/727) | | |
|
| • Links: NA | | |
| • reporting pathological note statusIV
| • Overall: 92% (670/727) | | |
|
| • Links: NA | | |
| • % quality of RT: wedges on tangent breast
fieldsIV
| • Overall: 92.8% (671/723) | | |
|
| • Links: NA | | |
| • % quality of RT: both tangent fields treated daily
IV
| • Overall: 99.9% (724/725) | | |
|
| • Links: NA | | |
| • % quality of RT: 4,500–5,000 cGy total breast dose
given to 180–200 cGy fractionsIV
| • Overall: 99% (723/725) | | |
|
| • Links: NA | | |
| • % quality of RT: electron beam breast radiation
usedIV
| • Overall: 94% (681/725) | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BC = breast cancer; enrolled = n qualified; evaluated = n
analyzed; ACR = American College of Radiology; ACS = American
College of Surgeons; CAP= College of American Pathologists; SSO =
Society of Surgical Oncology; ER = estrogen receptor; PR =
progesterone receptor; state of use = last 3 y; RT = radiotherapy;
Level Ia = pre-study data indicating consistently sound psychometric
properties; Iac = pre- and on-study data indicating
consistently sound psychometric properties; IV = no pre-
or on-study psychometric data |
Silliman, 1999, US |
Process:
| • Overall: 77.2% (234/303) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: convenience sample women ≥55 y newly
diagnosed stage I or II BC treated in 1/5 academic centers,
Boston |
| • % appropriate use of definitive locoregional therapy
(total mastectomy + ALND or BCS with ALND + RT) IV
| • by surgery type: | • Data sources: medical records; 35-minute
computer-assisted telephone interview with pts; Physicians Profiles
database of the Board of Registration in Medicine of the
Commonwealth of MA | • Exclusion: NR |
| | BCS + RT: 56% | • Developmental period: NR | • Period: NR |
| | Mastectomy: 22% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 303/303 |
| | • by income: | • Data sources: NR | • Age (mean & range): 67.7 (55–97) y |
| | ≤U$14,999: 55% | • Psychometric properties: NR | • Race: White (93%) |
| | $15,000–29, 999: 85% | • Links to outcomes: NR | • Case characteristics: stage I (64%) |
| | $30,000–49,999: 91% | • Funding source: NR | • Socioeconomic status: income: |
| | ≥$50,000: 87% | • State of use: NR | ≤ U$14,999 (17.5%); |
| | • by education: | • Current use: external quality oversight | $15,000–$29,999 (19.8%); |
| | <High school: 55% | • Care setting: hospitals; cancer centers; RT
centers | $30,000–$49,999 (21.1%); |
| | High school: 75% | • Professionals: oncologists; RT oncologists; GPs | >$50,000 (17.5%); married (48.8%); ≥ High school
(83%) |
| | Some College: 83% | | • Funding: NCI, NHI; US ARDALC |
| | College: 82% | | |
|
| • Links: NA | | |
| • % appropriate use of any adjuvant systemic therapy
(CT &/or HT) IV
| • Overall: 67.3% (204/303) | | |
| | • by adjuvant therapy: | | |
| | HT alone: 76% | | |
| | CT alone: 13% | | |
| | HT + CT: 11% | | |
| | • by income: | | |
| | ≤U$14,999: 64% | | |
| | $15,000–29,999: 60% | | |
| | $30,000–49,999: 77% | | |
| | ≥$50,000: 73% | | |
| | • by education: | | |
| | < High school: 60% | | |
| | High school: 68% | | |
| | Some College: 64% | | |
| | College: 72% | | |
|
| • Links: NA | | |
| • % appropriate use of alternative definitive therapy
(both tumor therapy & adjuvant systemic therapy)
IV
| • Overall: 51.8% (157/303) | | |
| | By age: | | |
| | 55–64 y: 50% (78/157) | | |
| | 65–74 y: 41% (65/157) | | |
| | 75–84 y: 9% | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; NCI = National Cancer Centre; NIH = National Health
Institute; ARDALC = Army Research, Development, Acquisition and
Logistic Command; MA = Massachusetts; state of use = last 3 y; GP =
general practitioner RT = radiotherapy; CT = chemotherapy; HT =
hormone therapy; BCS = breast-conserving surgery; ALND = axillary
lymph node dissection; Level Ia = pre-study data indicating
consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
Solin, 1999, US |
Process:
| • Overall: 65% (62/95) | • Standard: NIH Consensus Development Conference,
1990 | • Inclusion: convenience sample women ≥ 65 y, newly
diagnosed stage 0–II BC <5cm in diameter |
| • % appropriate use of
BCSIV
| • Links: NA | • Data sources: HMO claim database; medical
records | • Exclusion: LCIS; bilateral carcinoma |
| • % appropriate use of RT after BCSIV
| • Overall: 89% (55/62) | • Developmental period: NR | • Period: 2 y (1993-1994) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 130/130 |
| • % appropriate use of definite breast irradiation in
DCISIV
| • Overall: 60% (3/5) | • Data sources: NR | • Age (mean & range): 72 (65–91) y |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: White (83%); Black (5%) |
| • % appropriate use of definite breast irradiation in
stage I–II IV
| • Overall: 91% (52/57) | • Links to outcomes: NR | • Case characteristics: DCIS (6%); invasive BC (94%);
tumor size (<1cm 23%; 1.1–2 cm 26%; 2.1–3 cm 12%); stages
0–IV; node (-) (73%) |
| | • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: NR |
| | | • Current use: external quality oversight;
research | |
| | | • Care setting: hospitals; pathology centers; RT
centers; cancer centers | |
| | | • Professionals: pathologists; oncologists; surgeons;
GPs | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; BCS = breast-conserving surgery; RT = radiotherapy; DCIS =
ductal carcinoma in situ; BC = breast cancer; NIH = National
Institute of Health; state of use = last 3 y; GP = general
practitioner; HMO = health maintenance organization; LCIS = lobular
carcinoma in situ; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric
data |
Tyldesley, 2003,
Canada |
Process: | • Overall: 63% | • Standard: systematic review; evidence based
recommendations for BCS in North America (US & Canada); CPG
(n = 12); 1991-2001 | • Inclusion: population-based samples women ESBC
eligible for BCS in North American population |
| • % appropriate use of BCS in
DCIS; eligible & preferred*IV
| • Links: NA | • Data sources: several databases (SEER; OCR) | • Exclusion: NR |
| • % appropriate use of BCS in stage; eligible &
preferred**IV
| • Overall: 57% | • Developmental period: NR | • Period: NR |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): NR |
| • % appropriate use of BCS in stage II; eligible
& preferred**IV
| • Overall: 52% | • Data sources: NR | • Age (mean & range): NR |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % appropriate use of BCS in stage IIIA; eligible
& preferred***IV
| • Overall: 27% | • Links to outcomes: NR | • Case characteristics: ESBC including DCIS; stage
I–IIIA |
| | • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| | | • State of use: NR | • Funding: Cancer Care Ontario; NCI of Canada |
| | | • Current use: external quality oversight;
research | |
| | | • Care setting: cancer centers; hospitals; RT
centers | |
| | | • Professionals: oncologists; surgeons; RT
oncologists | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; RT = radiotherapy; CT = chemotherapy; HR = hormone
receptor; state of use = last 3; ER = estrogen receptor; PR =
progesterone receptor; BC = breast cancer; NCI = National Cancer
Institute; SEER = surveillance epidemiology end results; OCR =
Ontario cancer registry; BCS = breast-conserving surgery; DCIS =
ductal carcinoma in situ; SLE = systemic lupus erithematous; SS =
systemic sclerosis; *DCIS: low/moderate risk; not pregnant; no prior
RT; no SLE/SS; **Stage I: not pregnant; no prior RT; solitary
primary; no SLE/SS; negative margins; low tumor/breast size rate;
*** Stage IIIA: not pregnant; no prior RT; solitary primary tumor;
no SLE/SS; CR/PR (complete or partial response to neo-adjuvant CT
that eliminates the need for mastectomy; Level Ia = pre-study data
indicating consistently sound psychometric properties; Iac = pre-
and on-study data indicating consistently sound
psychometric properties; IV = no pre- or on-study
psychometric data |
White, 2003, US |
Process:
| • Overall: 88% | • Standard: ACOS; ACR; CAP; SSO standards for BCT,
1992 | • Inclusion: convenience sample women BC Stage I–II
diagnosed, 1994 |
| • % appropriate use of preoperative mammographic
evaluationIV
| • by age: | • Data sources: cancer registries of 842 US
hospitals | • Exclusion: incomplete pathologic reporting; not
appropriate candidates for BCT based on standards; stage III–IV |
| | <70 y: 88.5% | • Developmental period: NR | • Period: 1 y (1994) |
| | ≥70 y: 86.2% | • Reference standard(s) (publication date): NR | • n patients (enrolled/evaluated): 17,931/16,643 |
| | • by race/ethnicity: | • Data sources: NR | • Age (mean & range): 62 (21–>70) y |
| | White: 88.4% | • Psychometric properties: NR | • Race/ethnicity: White (85.9%), Black (7.8%), Hispanic
(2.9%), Asian (2%), other (1.3%) |
| | Black-H: 86.5% | • Links to outcomes: NR | • Case characteristics: NR |
| | other: 87.5% | • Funding source: NR | • Socioeconomic status: private insurance (34.5%); HMO
(14.7%); Medicare (42.1%); Medicaid (7%) |
| | • by payer: | • State of use: NR | • Funding: NCI |
| | Government: 87.7% | • Current use: quality of care reporting; external
quality oversight; research | |
| | Private: 88.7% | • Care setting: hospitals; RT centers; cancer
centers | |
|
| • Links: NA | • Professionals: RT oncologists; oncologists; surgeons;
GPs | |
| • % reporting size of mammographic abnormality
IV
| • Overall: 47% | | |
| | • by age: | | |
| | <70 y: 45.9% | | |
| | ≥70 y: 50.7% | | |
| | • by race/ethnicity: | | |
| | White: 47.5% | | |
| | Black-H: 46.3% | | |
| | other: 39.6% | | |
| | • by payer: | | |
| | Government: 50.3% | | |
| | Private: 44.8% S | | |
|
| • Links: NA | | |
| • % appropriate use of BCSIV
| • Overall: 42.6% | | |
| | • by age: | | |
| | <70 y: 46% | | |
| | ≥70 y: 34% | | |
| | • by race/ethnicity: | | |
| | White: 43% | | |
| | Black-H: 44% | | |
| | other: 36% | | |
| | • by payer: | | |
| | Government: 37% | | |
| | Private: 48% S | | |
|
| • Links: NA | | |
| • % reporting laterality of surgical
specimenIV
| • Overall: 98.3% | | |
| | • by age: | | |
| | <70 y: 98.2% | | |
| | ≥70 y: 98.6% | | |
| | • by race/ethnicity: | | |
| | White: 98.2% | | |
| | Black-H: 98.5% | | |
| | other: 99.3% | | |
| | • by payer: | | |
| | Government: 98.4% | | |
| | Private: 98.3% | | |
|
| • Links: NA | | |
| • % reporting identification of affected
quadrantIV
| • Overall: 21.1% | | |
| | • by age: | | |
| | <70 y: 21.1% | | |
| | ≥70 y: 21.3% | | |
| | • by race/ethnicity: | | |
| | White: 20.5% | | |
| | Black-H: 26.3% | | |
| | other: 21.5% | | |
| | • by payer: | | |
| | Government: 22% | | |
| | Private: 20.4% | | |
|
| • Links: NA | | |
| • % reporting pathological specimen
orientedIV
| • Overall: 67.1% | | |
| | • by age: | | |
| | <70 y: 68% | | |
| | ≥70 y: 64.9% | | |
| | • by race/ethnicity: | | |
| | White: 67.6% | | |
| | Black-H: 64.2% | | |
| | other: 71.5% | | |
| | • by payer: | | |
| | Government: 67.5% | | |
| | Private: 67.1% | | |
|
| • Links: NA | | |
| • % reporting carcinoma microscopically
confirmedIV
| • Overall: 97.8% | | |
| | • by age: | | |
| | <70 y: 97.7% | | |
| | ≥70 y: 97.9% | | |
| | • by race/ethnicity: | | |
| | White: 97.9% | | |
| | Black -H: 96.7% | | |
| | other: 99.3% | | |
| | • by payer: | | |
| | Government: 98.1% | | |
| | Private: 97.7% | | |
|
| • Links: NA | | |
| • % reporting histological typeIV
| • Overall: 98.8% | | |
| | • by age: | | |
| | <70 y: 98.8% | | |
| | ≥70 y: 98.7% | | |
| | • by race/ethnicity: | | |
| | White: 98.8% | | |
| | Black -H: 99% | | |
| | other: 99.3% | | |
| | • by payer: | | |
| | Government: 99% | | |
| | Private: 98.7% | | |
|
| • Links: NA | | |
| • % reporting histological gradeIV
| • Overall: 80.6% | | |
| | • by age: | | |
| | <70 y: 81.1% | | |
| | ≥70 y: 79.3% | | |
| | • by race/ethnicity: | | |
| | White: 80.5% | | |
| | Black -H: 79.7% | | |
| | other: 88.9% | | |
| | • by payer: | | |
| | Government: 80.1% | | |
| | Private: 81.2% | | |
|
| • Links: NA | | |
| • % reporting LV invasionIV
| • Overall: 53.5% | | |
| | • by age: | | |
| | <70 y: 54.3% | | |
| | ≥70 y: 51.5% | | |
| | • by race/ethnicity: | | |
| | White: 52.9% | | |
| | Black -H: 54.4% | | |
| | other: 70.8% | | |
| | • by payer: | | |
| | Government: 51.3% | | |
| | Private: 54.9% S: | | |
|
| • Links: NA | | |
| • % reporting size invasive carcinoma IV
| • Overall: 91.8% | | |
| | • by age: | | |
| | <70 y: 91.6% | | |
| | ≥70 y: 91.9% | | |
| | • by race/ethnicity: | | |
| | White: 91.7% | | |
| | Black -H: 91.2% | | |
| | other: 96.5% | | |
| | • by payer: | | |
| | Government: 91.6% | | |
| | Private: 92% | | |
|
| • Links: NA | | |
| • % reporting macroscopic margins of carcinoma
measuredIV
| • Overall: 72.4% | | |
| | • by age: | | |
| | <70 y: 72.5% | | |
| | ≥70 y: 72.1% | | |
| | • by race/ethnicity: | | |
| | White: 72.5% | | |
| | Black -H: 73.5% | | |
| | other: 61.8% | | |
| | • by payer: | | |
| | Government: 73.1% | | |
| | Private: 72.3% | | |
|
| • Links: NA | | |
| • % reporting microscopic margins
assessmentIV
| • Overall: 89.5% | | |
| | • by age: | | |
| | <70 y: 90% | | |
| | ≥70 y: 88.7% | | |
| | • by race/ethnicity: | | |
| | White: 89.7% | | |
| | Black -H: 86.8% | | |
| | other: 95.8% | | |
| | • by payer: | | |
| | Government: 89% | | |
| | Private: 90.2% | | |
|
| • Links: NA | | |
| • % reporting DCIS present/absentIV
| • Overall: 43.2% | | |
| | • by age: | | |
| | <70 y: 44.8% | | |
| | ≥70 y: 38.6% | | |
| | • by race/ethnicity: | | |
| | White: 43.3% | | |
| | Black -H: 40.8% | | |
| | other: 49.3% | | |
| | • by payer: | | |
| | Government: 40.2% | | |
| | Private: 45.7% S | | |
|
| • Links: NA | | |
| • % reporting ER statusIV
| • Overall: 91.7% | | |
| | • by age: | | |
| | <70 y: 91.9% | | |
| | ≥70 y: 91.2% | | |
| | • by race/ethnicity: | | |
| | White: 91.8% | | |
| | Black -H: 90.4% | | |
| | other: 96.5% | | |
| | • by payer: | | |
| | Government: 91.4% | | |
| | Private: 92.3% | | |
|
| • Links: NA | | |
| • % reporting PR statusIV
| • Overall: 90.6% | | |
| | • by age: | | |
| | <70 y: 90.9% | | |
| | ≥70 y: 89.7% | | |
| | • by race/ethnicity: | | |
| | White: 90.7% | | |
| | Black -H: 89.6% | | |
| | other: 95.1% | | |
| | • by payer: | | |
| | Government: 90.1% | | |
| | Private: 91.4% | | |
|
| • Links: NA | | |
| • % appropriate use of RT after BCSIV
| • Overall: 85.9% | | |
| | • by age: | | |
| | <70 y: 88.4% | | |
| | ≥70 y: 78.9% | | |
| | • by race/ethnicity: | | |
| | White: 86.3% | | |
| | Black -H: 83.2% | | |
| | other: 81.9% | | |
| | • by payer: | | |
| | Government: 83.3% | | |
| | Private: 88.6% S | | |
|
| • Links: NA | | |
| • % quality of RT: planning on a dedicated
simulatorIV
| • Overall: 88.9% | | |
| | • by age: | | |
| | <70 y: 89% | | |
| | ≥70 y: 88.8% | | |
| | • by race/ethnicity: | | |
| | White: 89% | | |
| | Black -H: 87.7% | | |
| | other: 87.3% | | |
| | • by payer: | | |
| | Government: 89.1% | | |
| | Private: 88.8% | | |
|
| • Links: NA | | |
| • % quality of RT: homogenous dose
distributionIV
| • Overall: 96.6% | | |
| | • by age: | | |
| | <70 y: 96.6% | | |
| | ≥70 y: 96.8% | | |
| | • by race/ethnicity: | | |
| | White: 96.6% | | |
| | Black -H: 96.5% | | |
| | other: 97.5% | | |
| | • by payer: | | |
| | Government: 96.7% | | |
| | Private: 96.7% | | |
|
| • Links: NA | | |
| • % quality of RT: done 5 d/wkIV
| • Overall: 97.4% | | |
| | • by age: | | |
| | <70 y: 97.4% | | |
| | ≥70 y: 97.4% | | |
| | • by race/ethnicity: | | |
| | White: 97.5% | | |
| | Black -H: 97.5% | | |
| | • by payer: | | |
| | Government: 97.1% | | |
| | Private: 97.1% | | |
|
| • Links: NA | | |
| • % quality of RT: use of wedges on tangent breast
fieldsIV
| • Overall: 93.4% | | |
| | • by age: | | |
| | <70 y: 93.3% | | |
| | ≥70 y: 93.8% | | |
| | • by race/ethnicity: | | |
| | White: 93.5% | | |
| | Black -H: 92.1% | | |
| | other: 97.5% | | |
| | • by payer: | | |
| | Government: 93% | | |
| | Private: 93.8% | | |
|
| • Links: NA | | |
| • % appropriate use of adjuvant systemic therapy in
node (+) after BCTIV
| • Overall: 84.1% | | |
| | • by age: | | |
| | <70 y: 84.9–88.7% | | |
| | ≥70 y: 72% | | |
| | • by race/ethnicity: | | |
| | White: 85.3% | | |
| | Black -H: 78.7% | | |
| | other: 78.3% | | |
| | • by payer: | | |
| | Government: 78.9% | | |
| | Private: 87.6% S | | |
| | • Links: NA | | |
|
NR = not reported; NA
= not assessed; S = significant difference/trend; NS =
nonsignificant difference/trend; n = number of patients; pts =
patients; enrolled = n qualified; evaluated = n analyzed; BC =
breast cancer; LV = Lymphatic/Vascular; ER = estrogen receptor; PR =
progesterone receptor; RT = radiotherapy; BCS = breast-conserving
surgery; ACOS = American Collage of Surgeons; node (+) = lymph node
positive; state of use = last 3 y; GP = general practitioner; NCI =
National Cancer Institute; CAP = Collage of American pathologists;
SSO = Society of Surgical Oncology; ACR = American Collage of
radiology; BCT = breast-conservation therapy; Level Ia = pre-study
data indicating consistently sound psychometric properties; Iac =
pre- and on-study data indicating consistently
sound psychometric properties; IV = no pre- or
on-study psychometric data |
Wilkinson, 2003, US |
Process:
| • Overall: 91% | • Standard: CAP guideline, 1998 | • Inclusion: convenience sample women stage I–II breast
infiltrative carcinoma referred to RPCI after excisional biopsy,
1998-1999 |
| • % reporting of size specimen in
3 dimensionsIV
| • Links: NA | • Data sources: cancer database of Department of
Surgery at Roswell Park Cancer Institute | • Exclusion: simultaneous axillary staging or
mastectomy performed; preceding FNA or CNB performed; carcinoma in
situ |
| • % reporting tumor sizeIV
| • Overall: 40% | • Developmental period: NR | • Period: 2 y (1998-1999) |
|
| • Links: NA | • Reference standard(s) (publication date): NR | • n patients: (enrolled/evaluated): 100/83 |
| • % reporting orientation of specimen (for margin
analysis) IV
| • Overall: 25% | • Data sources: NR | • Age (mean & range): NR |
|
| • Links: NA | • Psychometric properties: NR | • Race/ethnicity: NR |
| • % reporting microscopic margin statusIV
| • Overall: 94% | • Links to outcomes: NR | • Case characteristics: infiltrating carcinoma; stage
I–II |
|
| • Links: NA | • Funding source: NR | • Socioeconomic status: NR |
| • % reporting distance to closest marginIV
| • Overall: 69% | • State of use: NR | • Funding: NR |
|
| • Links: NA | • Current use: internal quality improvement; quality of
care reporting | |
| • % reporting specimen inkedIV
| • Overall: 77% | • Care setting: hospitals; cancer centers; pathology
centers | |
|
| • Links: NA | • Professionals: oncologists; pathologists;
surgeons | |
| • % reporting histology typeIV
| • Overall: 100% | | |
|
| • Links: NA | | |
| • % reporting histology gradeIV
| • Overall: 90% | | |
|
| • Links: NA | | |
| • % reporting tumor size (microscopic) IV
| • Overall: 90% | | |
|
| • Links: NA | | |
| • % reporting lymphovascular invasion
(presence/absence) IV
| • Overall: 47% | | |
|
| • Links: NA | | |
| • % reporting presence of in situ
componentIV
| • Overall: 71% | | |
|
| • Links: NA | | |
| • % reporting BSR scale (tumor grade) IV
| • Overall: 6% | | |
|
| • Links: NA | | |
| • % reporting TNM stagingIV
| • Overall: 9% | | |
| | • Links: NA | | |
|
NR = not reported; NA = not assessed; S =
significant difference/trend; NS = nonsignificant difference/trend;
n = number of patients; pts = patients; enrolled = n qualified;
evaluated = n analyzed; BC = breast cancer; RPCI = Roswell Park
Cancer Institute; FNA = fine-needle aspiration; CNB = core-needle
biopsy; CAP = College of American Pathologists; CPG = clinical
practice guideline; state of use = last 3 y; BSR = Bloom Scarf
Richardson Scale; Level Ia = pre-study data indicating consistently
sound psychometric properties; Iac = pre- and
on-study data indicating consistently sound psychometric properties;
IV = no pre- or on-study psychometric data |