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Meta-analysis for the evaluation of surrogate endpoints in cancer clinical trials

机译:荟萃分析评估癌症临床试验中的替代终点

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The identification and validation of putative surrogate endpoints in oncology is a great challenge to medical investigators, statisticians, and regulators. A putative surrogate endpoint must be validated at both individual-level and trial-level before it can be used to replace the clinical endpoint in a future clinical trial. Recently, meta-analytic methods for evaluating potential surrogates have become widely accepted in cancer clinical trials. In this review, after addressing multiple complications and general issues surrounding surrogate endpoints, we review various proposed and adopted meta-analytic methodologies pertaining to the application of these methods to oncology clinical trials with different tumor types. In oncology, several applications have successfully identified useful surrogates. For example, disease-free survival and progression-free survival have been validated through meta-analyses as acceptable surrogates for overall survival in adjuvant colon cancer and advanced colorectal cancer, respectively. We also discuss several limitations of surrogate endpoints, including the critical issues that the extrapolation of the validity of a surrogate is always context-dependent and that such extrapolation should be exercised with caution.
机译:肿瘤学中假定的替代终点的识别和验证对医学研究人员,统计学家和监管机构构成巨大挑战。推定的替代终点必须在个人水平和试验水平上均经过验证,然后才能在以后的临床试验中用于替代临床终点。近来,用于评估潜在替代物的荟萃分析方法已在癌症临床试验中被广泛接受。在这篇综述中,在解决了替代终点周围的多种并发症和一般性问题之后,我们回顾了与这些方法在不同肿瘤类型的肿瘤临床试验中的应用有关的各种拟议和采用的荟萃分析方法。在肿瘤学中,几种应用已成功地鉴定出有用的替代物。例如,无病生存率和无进展生存率已通过荟萃分析被确认为分别是佐剂结肠癌和晚期结直肠癌总体生存率的可接受替代指标。我们还将讨论代理端点的一些局限性,包括以下关键问题:代理有效性的外推始终取决于上下文,并且应谨慎进行此类外推。

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