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Belinson S, Chopra R, Yang Y, et al. Local Hepatic Therapies for Metastases to the Liver From Unresectable Colorectal Cancer [Internet]. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Dec. (Comparative Effectiveness Reviews, No. 93.)
This publication is provided for historical reference only and the information may be out of date.
Local Hepatic Therapies for Metastases to the Liver From Unresectable Colorectal Cancer [Internet].
Show detailsIn this chapter, we present the results of our systematic review of the literature and synthesis of the extracted data on outcomes on the effectiveness and comparative effectiveness of local hepatic therapy for unresectable CRC metastases to the liver. The Key Questions (KQs) for this review are: KQ1 (effectiveness) and KQ2 (harms) of local hepatic therapy for unresectable CRC metastases to the liver in patients whose disease is refractory to systemic chemotherapy and who have no or minimal extrahepatic disease; and KQ3 (effectiveness) and KQ4 (harms) of local hepatic therapy for unresectable CRC metastases to the liver in patients who are also receiving systemic chemotherapy and have no extrahepatic disease.
We first describe the results of our literature searches and then present the results for KQ1 and KQ2, which include a list of key points, an overview of the included literature, and a detailed synthesis of the data. This is followed by the same for KQ3 and KQ4. We identified 937 nonduplicate titles or abstracts with potential relevance, and of these, 189 proceeded to full-text review (Figure 3). Thirty-one articles were included in the review, including one hand-searched article and five articles from gray literature identified through other sources (the American Society of Clinical Oncology, American Society of Clinical Oncology Gastrointestinal Cancers, Surgical Society of Oncology, and Radiosurgical Society). The 31 arms represent 30 distinct studies: 1 RCT, 12 prospective case series, and 17 retrospective case series. Twenty-three studies pertain to KQ1, 23 studies to KQ2, 7 studies to KQ3, and 7 studies to KQ4.
Results of Literature Searches
Of the 937 records identified through the literature search, we excluded 913 at various stages of screening and included 24 records.63–86 We included one hand-searched article,87 two published studies from scientific information packets,88,89 and three articles from conference abstracts.90–92 A total of 30 articles were included in this report: 29 case-series and one RCT87 for which a single arm was abstracted as a case series. This RCT compared RFA with systemic chemotherapy to systemic chemotherapy alone. The scope of the review was liver-directed therapy versus liver-directed therapy. Systemic chemotherapy alone was not a relevant intervention or comparator for this review. Only the RFA combined with systemic chemotherapy arm was abstracted and included in this report as it is relevant for KQ3 and KQ4.
The PRISMA diagram (Figure 3) depicts the flow of search screening and study selection.53 A list of full-text studies with reason for exclusion is presented in Appendix F.
Our searches of various gray literature sources yielded five published studies that we added to the articles identified in the search of publications databases and that were included in the analyses presented in this evidence review.88–92
We evaluated the results of the gray literature search as follows:
- Regulatory information: The search yielded six results, but no new studies were identified from this source.
- Clinical trial registries (ClinicalTrials.gov): The search yielded 259 clinical trials; we excluded 219 trials during the title and abstract screen. Twenty-five of the remaining 40 trials were excluded. Among the 15 trials remaining, 2 contained too little information to make a conclusion about their relevance to the KQs of this report. Of the remaining 13 studies, three had been terminated, seven were ongoing or recruiting, and three had been completed. We found no publications for the three completed trials. All terminated studies cited low recruitment as the reason for study termination.
- Abstracts and conference papers: The search yielded 174 citations, and we excluded 132 during the title and abstract screen. Of the remaining 42 items, two were duplicates and 37 did not meet inclusion criteria after full-text review. The three remaining references met all inclusion criteria and were included in this report.90–92
- Manufacturer database: Scientific information packets were received from Accuray (manufacturers of the CyberKnife® SBRT system) and SIRTEX (manufacturers of the Yttrium-90–infused SIR-Spheres microspheres). The submissions consisted of 55 published references, listings of clinical trials, or conference abstracts. Of the 55 references, we excluded 53 during the abstract and title screen. The remaining two references met the inclusion criterion and were included in this report.88,89
Overview of the Literature
Thirty-one arms within 30 studies met our inclusion criteria and addressed local hepatic therapy for unresectable CRC metastases to the liver. Nine studies were conducted in the United States, four in Italy, four in Germany, three in Australia, three in Japan, two in the United Kingdom, two in Korea, and one study each in France, the Netherlands, and Turkey (Table 4). The number of patients in each study ranged from 6 to 140.
All 30 studies had clearly defined questions and well-described interventions, used validated outcome measures, and had conclusions that were supported by the data. Studies varied on how well they described the study population, how well they described their results, and acknowledgement of sponsorship and funding. Fifteen studies did not have well-described patient populations,63,65,67,70,74,78,79,81,83–86,88,89,91 and three studies lacked well-described results.67,70,74
Fifteen studies were rated as good quality,64,66,68,69,71–73,75–77,80,82,87,90,92 12 studies as fair quality,57,63,65,78,79,81,84–86,88,89,91 and three as poor quality.67,70,74
Key Questions 1 and 2. Effectiveness and Harms of Therapies in Patients Refractory to Systemic Chemotherapy
KQs 1 and 2 focus on the comparative effectiveness (KQ1) and harms (KQ2) of the various local hepatic therapies in patients with unresectable colorectal cancer (CRC) metastases to the liver and who have minimal evidence of extrahepatic disease and whose disease is refractory to systemic therapy (i.e., are not eligible to receive systemic chemotherapy).
Key Points
- The evidence is insufficient to draw conclusions about overall survival, quality of life, or adverse events. Due to the absence of comparative data, we are limited in drawing conclusions regarding the efficacy and effectiveness of these interventions. Risk of bias is a primary concern in observational studies. Intended effects are likely to be biased by preferential prescribing of the intervention based on the patients’ prognosis.
- The assessment of applicability of the study findings to clinical practice is limited by the poor characterization of the patient populations (e.g., number and size of metastases, performance status) and variability in the delivery of the interventions (e.g., surgical approach, dose and drugs delivered).
Description of Included Studies
Twenty-three case series63,65–71,73–78,82–84,86,88–92 met inclusion criteria to address KQ1 and KQ2. Of the 23 case series, nine were prospective66,67,70,73–76,78,88 and 14 were retrospective.63,65,68,69,71,77,82–84,86,89–92 The total number of patients for whom data were abstracted from the 23 studies was 932. Three studies included patients treated with TACE with DEB;67,75,90 and two articles reported on TACE alone;63,68 three on SBRT;71,82,88 thirteen on RE;65,66,68,70,73,76–78,84,86,89,91,93 two on HAI,83,92 and one on RFA.69 All studies initiated treatment in patients after January 1, 2000, except for the study by Albert and colleagues21 on TACE. We included this study because it reported on relatively large numbers of patients treated, and analyses showed no differences in outcomes before and after 2000. Table 5 shows the summary of the study and patient characteristics, including number of patients enrolled, study design, intervention period, and intervention, and patient demographics.
Patients ranged in age from 30 to 91 years, but they were generally in their late 50s or early 60s. Thirteen studies reported rates of previous resection that ranged from 2.6 to 83.5 percent.63,64,66,68–70,75,82,84,88,89,91,92 Five studies reported median ECOG scores of 0–1, with a range of 0–3.66,67,73,75,77 In all but two studies,72,81 patients had been treated with prior lines of systemic chemotherapy, and 11 studies reported patient experience with prior local hepatic therapy.63,68–70, 75,78,82,84,88,89,91 Lines of previous systemic chemotherapy are presented in Appendix D.
The included evidence is clinically diverse with respect to the number of patients undergoing previous resection and local hepatic therapy. Variations are also present in the treatments—in terms of the drugs or dosage—within a given intervention.
Data on tumor characteristics were inconsistently reported across studies and are detailed in Table 6. Synchronous or metachronous disease status was reported in eight studies and synchronous disease ranged from 17 to 73 percent.66,68,71,75,83,91,92,94 Bilobar or unilobar disease was reported in six studies and bilobar disease ranged from 66.7 to 95.1 percent.65,66,68,73,76,86 Eight studies reported liver involvement, but used nonuniform measurements.65,67,70,73,75–77,90 Four studies reported mean or median number of hepatic lesions.69,71,75,82 Six studies reported the mean size of hepatic lesions, which ranged from 2.9 to 12cm.66,68,69,82,90,94 Presence of extrahepatic metastases were reported by five studies and ranged from 33 to 81 percent of patients.63,66,68,91,92 Although extrahepatic disease was reported by these studies, the patients were all described as having liver-dominant disease (i.e., majority of the disease is confined to the liver).
Detailed Synthesis
Table 7 displays the outcomes reported. All studies reported overall survival. All studies reported on adverse events, but four studies aggregated these events by multiple primary cancer sites, which did not permit us to extract CRC-specific adverse events.69,70,77,78 Eight studies also reported progression-free survival.63,65,66,71,75,90,92,93 Three studies reported on both liver-specific progression-free survival and overall progression-free survival;63, 75, 92 no studies reported on liver-specific progression-free survival alone; and the remaining five studies reported overall progression-free survival alone.65,66,71,74,90 Jakobs et al. (2006)69 attempted to calculate the time to recurrence statistic but were unable to do so because of the low rate of recurrence (18%). Two studies reported on length of stay,63,67 and two studies reported on quality of life.66,67 We report data on individual outcomes, except for results on overall progression-free survival and liver-specific progression-free survival, which are located in Appendix D.
Overall Survival
All studies reported on outcomes related to overall survival (Table 8, which is organized by intervention). One RFA study by Jakobs et al. (2006)69 did not report mean or median survival measures, but did report 1-, 2-, and 3-year survival rates of 96 percent, 71 percent, and 68 percent, respectively, from the time of study treatment. Three studies in our report used TACE with DEB. Median survival was reported by two75,90 studies and ranged from 19 to 25 months from study treatment. Florentini et al. (2007) reported only a 1-year survival rate of 61 percent.67 Two studies reported on TACE alone.63,68 Both studies reported median survival from time of diagnosis of liver metastases, which ranged from 26.3 to 27 months. Thirteen studies of RE with Yttrium-90 were included in this review.65,66,68,70,73,74,76–78,84,86,89,91 One of these studies involved systemic chemotherapy in addition to RE and is therefore not presented in this summary of results.30 Eight studies reported survival from study treatment; median survival ranged from 4 to 15.2 months.70,73,77,78,84,86,89,91 One of these studies84 did not reach median survival at a follow up of 3 years. Three studies reported survival starting from diagnosis of liver metastases, which ranged from 31 to 34.6 months.66,68,76 Two studies did not indicate the time point from which survival was measured.65,74 HAI was used in two studies in our review,83,92 and reported median survival from the start of study treatment as 6.7 and 9.7 months.83,92 Three studies reported SBRT in this review and all defined survival from time of study treatment.71,82,88 Median survival values reported in two studies were 17 and 25 months.71,88 The third SBRT study only reported 1- and 2-year survival rates of 95 percent and 58 percent, respectively.82
Direct comparisons of overall survival cannot be made from the published data because there are no comparative studies and the studies measured survival from different starting points (i.e., time of diagnosis or time of treatment).
Quality of Life
Two studies reported on quality of life.66,67 Cosimelli and colleagues used a battery of questionnaires to assess both cancer and disease-specific quality of life (The European Organization for Research and Treatment of Cancer [EORTC] Quality of Life Questionnaire [QLQ] C30, EORTC QLQ C38, and EORTC QLQ LMC-21).66 They also assessed anxiety and depression (Hamilton Rating Scale for Depression [HAM-D]) and patient satisfaction (EORTC QLQ SAT-32). They reported quality of life measures on 14 of 50 enrolled subjects. The study authors provided no insight as to why only 14 of the participants had available data on quality of life. Six weeks after treatment, the quality of life of 14 patients treated with RE was not adversely affected, and patients’ anxiety levels were significantly reduced from pretreatment levels. No significant difference was observed in depression score pre- and post-treatment. In a study of chemoembolization with irinotecan-eluting beads, Fiorentini and colleagues stated that 18 of 20 patients reported improvement in quality of life post-treatment.41 They used the Edmonton Symptom Assessment System in this study, but only reported qualitatively that these patients had improved without providing any metrics.
Length of Stay
Mean length of stay was reported by two studies63,67 of TACE and ranged from 1.3 to 3 days. No direct comparisons can be made based on the published studies.
Time to Progression
Time to progression was not reported in any of the included studies.
Local Recurrence
Outcomes related to local recurrence are summarized in Table 9. In this report, local recurrence is defined as recurrence of the liver metastases in the area previously treated. This constitutes a treatment failure or failure to treat the entire lesion and is considered an adverse event. One RFA study reported a local recurrence rate of 18 percent.69 Local recurrence was also reported in two studies of SBRT, both of which reported a rate of 33.3 percent.71,88
Adverse Events
Twenty-four studies reported on adverse events with varying levels of detail and are presented in Table 9 by intervention. One TACE study reported a patient who developed a hepatic abscess.67 Liver failure was reported in three studies, two on RE65,66 and one75 on TACE with DEB intervention. Two studies—one on TACE63 and one on RE76—reported elevated alkaline phosphatase levels. Elevated bilirubin was reported in five studies, one on TACE with DEB90, one on TACE63, two on RE76,91, and one on HAI92. Elevated transaminase levels were reported in one RE article,76 which also reported elevated bilirubin and alkaline phosphatase. Although these results from liver function tests could point to disease progression, in the time period following a local hepatic therapy they are more likely to reflect an adverse effect of the treatment. Only Aliberti et al. reported liver function test results immediately after treatment.90 Other liver function tests were evaluated as acute or late toxicity76,91 or were not reported63,92 at the time adverse events were evaluated. Two authors indicated that liver function toxicity was likely a result of progressive disease or biliary obstruction.76,91 One TACE with DEB study reported one death from myocardial infarction75 and one TACE study reported a 30-day morality rate of 3.6 percent.63 A description of rare adverse events is included in Table 9. No study reported on injury to adjacent organs, hepatic hemorrhage, or steatohepatitis.
Multivariate Analyses
Univariate or multivariate analyses of prognostic factors for overall survival including, but not limited to, ECOG score, presence of extrahepatic disease, and treatment response, were variously reported in six case series63,73,76,78,91,92 of local hepatic therapies. All analyses reported on overall survival as the dependent variable.
Among the patient or tumor characteristics found to be associated with improved overall survival were the following: ECOG status (0 vs. ≥1 and in another study 0 or 1 vs. ≥2), performance status (0 or 1 vs. ≥ 2), number of extrahepatic metastases sites (0 or 1 vs. ≥2), number of lines of previous chemotherapy (0–1 vs. ≥ 2), performance status (0 or 1 vs. ≥ 2), carcinoembryonic antigen response (Yes, No), and Response Evaluation Criteria in Solid Tumors (RECIST).
Key Questions 3 and 4
Key Questions 3 and 4 focus on the comparative effectiveness (KQ3) and harms (KQ4) of the various local hepatic therapies in patients who are receiving local hepatic therapy as an adjunct to systemic therapy for unresectable CRC metastases to the liver and who have no evidence of extrahepatic disease.
Key Points
- No conclusions on overall survival, quality of life, length of stay, time to recurrence, local recurrence, or adverse events can be drawn from the body of evidence comparing local hepatic therapies for unresectable CRC metastases to the liver. No comparative studies met the inclusion criteria for this review.
- The assessment of applicability of the study findings to clinical practice is limited by the poor characterization of the patient populations (e.g., number and size of metastases, performance status) and variability in the delivery of the interventions (e.g., surgical approach, dose and drugs delivered)
Description of Included Studies
Table 10, Table 11, and Table 12 show the study, patient, and tumor characteristics, including study design, intervention period, intervention, number of patients enrolled, and patient demographics for studies of local hepatic therapies for patients with unresectable CRC metastases to the liver who are receiving local hepatic therapy as an adjunct to systemic therapy. Table 13 through Table 15 present data on study outcomes. Seven studies were included, 64,72,79–81,85,87 six of which were case series. One RCT87 was included in the review but was abstracted as a case-series study because the comparator, systemic chemotherapy, was an intervention outside the scope of this review. Of the six case series, three were prospective64,80,81 and three were retrospective.72,79,85 The total number of patients for which data were abstracted from the five studies was 296. Two studies included patients treated with RE with concurrent systemic chemotherapy;64,72 three articles reported on RFA with chemotherapy;80,85,87 and two reported on patients treated with HAI and systemic chemotherapy.79,81 All studies treated patients after January 1, 2000.
Patients ranged in age from 31 to 84 years, but were generally in their 60s. One study reported the ECOG score, with a median value of 0 and a range of 0 to 2.64 Two studies reported rates of resection for previous CRC liver metastases of 15 and 27 percent,64,87 and three studies64,72,80 reported the proportion of patients who had received prior systemic chemotherapy, which ranged from 0 to 94 percent. One study64 reported patient experience with prior local hepatic therapy, with 66 percent of patients having prior RE and 6 percent having had prior ablation.
Tumor characteristics were inconsistently reported across studies, with synchronous or metachronous disease status reported in three studies72,85,87; bilobar or unilobar disease reported in two studies;64,85 degree of liver involvement reported in three studies;64,72,79 number of hepatic lesions reported by two studies;80,87 and lesion size reported in two studies.80,85 The details of these characteristics are presented in Table 12.
Detailed Synthesis
Table 13 displays the outcomes reported by study for KQ3 and KQ4. All studies reported overall survival and adverse events. Four studies reported on overall progression-free survival.72, 79, 80, 87 Local recurrence was reported in three studies.64, 85, 87 One study reported on quality of life.87 We report data on individual outcomes, except for results on overall progression-free survival and liver-specific progression-free survival, which are located in Appendix D. No study reported on median time to recurrence, length of stay, or liver progression-free survival.
Overall Survival
Outcomes related to overall survival are summarized in Table 14, which is organized by intervention. All studies reported median overall survival. No direct comparisons can be made from the published data.
RFA was performed in three studies as an adjunct to systemic chemotherapy for unresectable CRC liver metastases.80,85,87 Ruers et al. (2012) reported a median survival of 45.3 months from time of randomization; Lee et al. (2012) reported a median survival of 24 months and Sgouros et al. (2011) reported a median survival of 24 months from study enrollment. Radioembolization was given as an adjunct to systemic chemotherapy in two studies, both of which reported survival from time of study treatment with a range of 9 to 37.8 months.64,72 HAI as an adjunct to systemic chemotherapy was reported in two studies. In both studies, the authors did not report the time point from which survival was measured.79,81 Survival ranged from 22 to 30.1 months.
Quality of Life
One study by Ruers and colleagues87 reported on the outcome of quality of life for patients treated with RFA and concurrent systemic chemotherapy. Quality of life was assessed by the EORTC QLQ-C30 questionnaire at baseline, every 6 weeks during study treatment, and during study followup. A 20-point difference is considered a significant change. Of the 60 patients enrolled, it is unclear how many of them were included in the analysis of quality of life. For those with available data, health-related quality of life declined 27 points following RFA. At 4 to 8 weeks post-RFA, prior to the start of systemic chemotherapy, the scores had risen to approximately 10 points below baseline. No other studies reported on quality of life and no direct comparisons can be made based on the published evidence.
Length of Stay
Mean length of stay was not reported by any studies.
Time to Recurrence
Time to recurrence was not reported in any of the included studies.
Local Recurrence
Outcomes related to local recurrence are summarized in Table 15. In this report, local recurrence is defined as recurrence of the liver metastases in the area previously treated. This constitutes a treatment failure or failure to treat the entire lesion and is considered an adverse event. Three RFA studies reported local recurrence rates between 45 and 81.3 percent.64,85,87
Adverse Events
Outcomes related to adverse events are summarized in Table 15, which is organized by intervention. One study of RE and one study of RFA reported injury to adjacent organs and liver failure.72,80 Elevated bilirubin was reported in two studies72,87 and elevated alkaline phosphatase and transaminases were reported in one study.72 Kosmider et al.72 reported elevated liver function test results within 60 days post-treatment that were not related to progressive disease and normalized shortly thereafter; Ruers et al.87 did not report when the patients had hepatic dysfunction related to elevated bilirubin. Lee et al. reported one patient (3.6 percent) who suffered from a 10-cm subcapsular hematoma.85 Local recurrence was reported by three studies.64,85,87 A single postoperative death was reported in two RFA studies.80,87 No direct comparisons can be made based on the published evidence.
Multivariate Analyses
Relevant univariate or multivariate analyses of prognostic factors for overall survival including, but not limited to, ECOG score, presence of extra hepatic disease, and treatment response, were reported in one case-series study52 of RE for unresectable CRC metastasis to the liver among patients who are candidates for local hepatic therapy as an adjunct to systemic therapy (Appendix D). These analyses reported on overall survival as the dependent variable; none evaluated factors associated with frequency of adverse events. Among the patient or tumor characteristics found to be associated with overall survival were extrahepatic disease (no vs. yes) and treatment response (complete vs. partial). Although these analyses may be hypothesis generating, they do not address the comparative benefit of radiotherapy techniques.
Overall Conclusions for Key Questions 1–4
- The body of evidence is insufficient to assess effectiveness or comparative effectiveness based on overall survival, quality of life, length of stay, time to progression, local recurrence, and adverse events for local hepatic therapy for the treatment of unresectable CRC metastases to the liver among patients whose disease is refractory to systemic therapy.
- The body of evidence is insufficient to assess effectiveness or comparative effectiveness based on overall survival, quality of life, length of stay, time to recurrence, local recurrence and adverse events for local hepatic therapy as an adjunct to systemic therapy for the treatment of unresectable CRC metastases to the liver.
- The assessment of applicability of the study findings to clinical practice is limited by the poor characterization of the patient populations (e.g., number and size of metastases, performance status) and variability in the delivery of the interventions (e.g., surgical approach, dose and drugs delivered).
For all Key Questions, we could only find case-series evidence that met inclusion criteria. There were no comparative studies, which limits our ability to draw conclusions for all key questions.
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