The role of biological therapy in metastatic colorectal cancer after first-line treatment: a meta-analysis of randomised trials

被引:29
|
作者
Segelov, E. [1 ]
Chan, D. [2 ]
Shapiro, J. [3 ]
Price, T. J. [4 ]
Karapetis, C. S. [5 ]
Tebbutt, N. C. [6 ]
Pavlakis, N. [2 ]
机构
[1] Univ New S Wales, St Vincents Clin Sch, Sydney, NSW 2052, Australia
[2] Royal N Shore Hosp, Sydney, NSW 2065, Australia
[3] Monash Univ, Cabrini Hosp, Melbourne, Vic 3800, Australia
[4] Univ Adelaide, Queen Elizabeth Hosp, Woodville, SA 5011, Australia
[5] Flinders Univ S Australia, Flinders Med Ctr, Flinders Ctr Innovat Canc, Bedford Pk, SA 5042, Australia
[6] Austin Hlth, Heidelberg, Vic 3084, Australia
关键词
colorectal; biological; meta-analysis; PHASE-III; WILD-TYPE; 2ND-LINE TREATMENT; RAS MUTATIONS; FLUOROURACIL; LEUCOVORIN; IRINOTECAN; CETUXIMAB; PLACEBO; KRAS;
D O I
10.1038/bjc.2014.404
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Biologic agents have achieved variable results in relapsed metastatic colorectal cancer (mCRC). Systematic meta-analysis was undertaken to determine the efficacy of biological therapy. Methods: Major databases were searched for randomised studies of mCRC after first-line treatment comparing (1) standard treatment plus biologic agent with standard treatment or (2) standard treatment with biologic agent with the same treatment with different biologic agent(s). Data were extracted on study design, participants, interventions and outcomes. Study quality was assessed using the MERGE criteria. Comparable data were pooled for meta-analysis. Results: Twenty eligible studies with 8225 patients were identified. The use of any biologic therapy improved overall survival with hazard ratio (HR) 0.87 (95% confidence interval (CI) 0.82-0.91, P<0.00001), progression-free survival (PFS) with HR 0.71 (95% CI 0.67-0.74, P<0.0001) and overall response rate (ORR) with odds ratio (OR) 2.38 (95% CI 2.03-2.78, P<0.00001). Grade 3/4 toxicity was increased with OR 2.34. Considering by subgroups, EGFR inhibitors (EGFR-I) in the second-line setting and anti-angiogenic therapies (both in second-line and third-line and beyond settings) all improved overall survival, PFS and ORR. EGFR-I in third-line settings improved PFS and ORR but not OS. Conclusions: The use of biologic agents in mCRC after first-line treatment is associated with improved outcomes but increased toxicity.
引用
收藏
页码:1122 / 1131
页数:10
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