伊立替康
西妥昔单抗
医学
克拉斯
内科学
肿瘤科
奥沙利铂
结直肠癌
荟萃分析
化疗
置信区间
癌症
作者
Sandro Barni,Mara Ghilardi,Karen Borgonovo,Mary Cabiddu,Alberto Zaniboni,Fausto Petrelli
出处
期刊:Reviews on Recent Clinical Trials
[Bentham Science]
日期:2013-10-01
卷期号:8 (2): 101-109
被引量:8
标识
DOI:10.2174/15748871113089990042
摘要
Cetuximab and irinotecan are effective agents in advanced colorectal cancer (CRC) after either irinotecanor oxaliplatin-based first-line chemotherapy. Here, the efficacy of this combination in patients with the KRAS wild-type gene as second- or further-line therapy is reviewed and data are collected in a pooled analysis.Studies that enrolled pretreated CRC patients for second-line therapy or beyond were identified using electronic databases (PubMed and EMBASE). A systematic analysis was conducted using Comprehensive Meta Analysis (version 2.2.064) to calculate the event rate of response and the 95% confidence interval. The weighted median overall survival (OS) and progression-free survival (PFS) were also calculated with NCSS 2007 software. We tested for significant heterogeneity using Cochran's chi-square test and the I(2) index.Twenty-five studies published between 2007 and 2012 were eligible for this analysis, with a total of 1,712 KRAS wild-type patients enrolled. The overall response rate was 31.9% with similar response rates of 28. 7% for second-line treatment and 31.1% for third or further lines. The overall weighted median OS and PFS were 12.5 and 6 months with a weighted OS of 11.56 and 12.2 months for second- and further-line CRC settings, respectively.In metastatic KRAS wild-type CRC patients pretreated with one or more lines of therapy, cetuximab plus irinotecan-based chemotherapy is an active treatment. Response rates and survival outcomes appear similar in second-line therapy or beyond.
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