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肿瘤学中评估总体生存替代终点的荟萃分析评价综述。

Review of meta-analyses evaluating surrogate endpoints for overall survival in oncology.

机构信息

RTI Health Solutions, Biometrics, Research Triangle Park, NC, USA.

出版信息

Onco Targets Ther. 2012;5:287-96. doi: 10.2147/OTT.S36683. Epub 2012 Oct 23.

Abstract

Overall survival (OS) is the gold standard in measuring the treatment effect of new drug therapies for cancer. However, practical factors may preclude the collection of unconfounded OS data, and surrogate endpoints are often used instead. Meta-analyses have been widely used for the validation of surrogate endpoints, specifically in oncology. This research reviewed published meta-analyses on the types of surrogate measures used in oncology studies and examined the extent of correlation between surrogate endpoints and OS for different cancer types. A search was conducted in October 2010 to compile available published evidence in the English language for the validation of disease progression-related endpoints as surrogates of OS, based on meta-analyses. We summarize published meta-analyses that quantified the correlation between progression-based endpoints and OS for multiple advanced solid-tumor types. We also discuss issues that affect the interpretation of these findings. Progression-free survival is the most commonly used surrogate measure in studies of advanced solid tumors, and correlation with OS is reported for a limited number of cancer types. Given the increased use of crossover in trials and the availability of second-/third-line treatment options available to patients after progression, it will become increasingly more difficult to establish correlation between effects on progression-free survival and OS in additional tumor types.

摘要

总生存期(OS)是衡量癌症新药治疗效果的金标准。然而,实际因素可能会妨碍无偏 OS 数据的收集,因此通常会使用替代终点。荟萃分析已广泛用于替代终点的验证,特别是在肿瘤学领域。本研究回顾了已发表的关于肿瘤学研究中使用的替代指标类型的荟萃分析,并考察了不同癌症类型的替代终点与 OS 之间的相关性程度。2010 年 10 月进行了检索,以根据荟萃分析汇总英文文献中关于将疾病进展相关终点作为 OS 替代终点的验证的现有证据。我们总结了已发表的荟萃分析,这些分析量化了多种晚期实体瘤类型中基于进展的终点与 OS 之间的相关性。我们还讨论了影响这些发现解释的问题。无进展生存期是晚期实体瘤研究中最常用的替代指标,并且仅针对少数几种癌症类型报告了与 OS 的相关性。鉴于试验中交叉的使用增加以及进展后患者可获得二线/三线治疗选择,在其他肿瘤类型中建立无进展生存期和 OS 之间的相关性将变得越来越困难。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6ec/3481854/2496b8b2f10c/ott-5-287f1.jpg

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