首页> 外文OA文献 >Individual Patient Data Analysis of Progression-Free Survival Versus Overall Survival As a First-Line End Point for Metastatic Colorectal Cancer in Modern Randomized Trials: Findings From the Analysis and Research in Cancers of the Digestive System Database
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Individual Patient Data Analysis of Progression-Free Survival Versus Overall Survival As a First-Line End Point for Metastatic Colorectal Cancer in Modern Randomized Trials: Findings From the Analysis and Research in Cancers of the Digestive System Database

机译:无进展生存期与总体生存期的个体患者数据分析,作为现代随机试验中转移性结直肠癌的一线终点:来自消化系统数据库癌症分析和研究的结果

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摘要

Purpose Progression-free survival (PFS) has previously been established as a surrogate for overall survival (OS) for first-line metastatic colorectal cancer (mCRC). Because mCRC treatment has advanced in the last decade with extended OS, this surrogacy requires re-examination. Methods Individual patient data from 16,762 patients were available from 22 first-line mCRC studies conducted from 1997 to 2006; 12 of those studies tested antiangiogenic and/or anti-epidermal growth factor receptor agents. The relationship between PFS (first event of progression or death) and OS was evaluated by using R-2 statistics (the closer the value is to 1, the stronger the correlation) from weighted least squares regression of trial-specific hazard ratios estimated by using Cox and Copula models. Results Forty-four percent of patients received a regimen that included biologic agents. Median first-line PFS was 8.3 months, and median OS was 18.2 months. The correlation between PFS and OS was modest (R-2, 0.45 to 0.69). Analyses limited to trials that tested treatments with biologic agents, nonstrategy trials, or superiority trials did not improve surrogacy. Conclusion In modern mCRC trials, in which survival after the first progression exceeds time to first progression, a positive but modest correlation was observed between OS and PFS at both the patient and trial levels. This finding demonstrates the substantial variability in OS introduced by the number of lines of therapy and types of effective subsequent treatments and the associated challenge to the use of OS as an end point to assess the benefit attributable to a single line of therapy. PFS remains an appropriate primary end point for first-line mCRC trials to detect the direct treatment effect of new agents. (C) 2014 by American Society of Clinical Oncology
机译:目的先前已建立无进展生存期(PFS)作为一线转移性结直肠癌(mCRC)总体生存期(OS)的替代物。由于近十年来随着mOS的延长OS对mCRC的治疗不断发展,因此这种代孕需要重新检查。方法从1997年至2006年进行的22项一线mCRC研究中,获得了16762名患者的个人患者数据。这些研究中的12个测试了抗血管生成和/或抗表皮生长因子受体药物。 PFS(进展或死亡的首发事件)与OS之间的关系是通过使用R-2统计量(值越接近1,相关性越强)对RFS统计量进行评估的,R-2统计量是通过使用Cox和Copula模型。结果44%的患者接受了包括生物制剂的治疗方案。一线PFS中位数为8.3个月,OS中位数为18.2个月。 PFS和OS之间的相关性中等(R-2,0.45至0.69)。分析仅限于使用生物制剂进行治疗的试验,非策略试验或优势试验不能改善代孕。结论在现代mCRC试验中,首次进展后的生存时间超过首次进展的时间,在患者和试验水平上,OS和PFS之间均呈正相关但适度的相关性。这一发现表明,由治疗路线的数量和有效的后续治疗类型引起的OS的实质性差异,以及使用OS作为评估单一治疗方案的获益终点的相关挑战。对于一线mCRC试验,PFS仍然是合适的主要终点,以检测新药的直接治疗效果。 (C)2014年美国临床肿瘤学会

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