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用于随机临床试验替代终点的荟萃分析评估的统一程序。

A unified procedure for meta-analytic evaluation of surrogate end points in randomized clinical trials.

机构信息

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

Biostatistics. 2012 Sep;13(4):609-24. doi: 10.1093/biostatistics/kxs003. Epub 2012 Mar 6.

Abstract

The meta-analytic approach to evaluating surrogate end points assesses the predictiveness of treatment effect on the surrogate toward treatment effect on the clinical end point based on multiple clinical trials. Definition and estimation of the correlation of treatment effects were developed in linear mixed models and later extended to binary or failure time outcomes on a case-by-case basis. In a general regression setting that covers nonnormal outcomes, we discuss in this paper several metrics that are useful in the meta-analytic evaluation of surrogacy. We propose a unified 3-step procedure to assess these metrics in settings with binary end points, time-to-event outcomes, or repeated measures. First, the joint distribution of estimated treatment effects is ascertained by an estimating equation approach; second, the restricted maximum likelihood method is used to estimate the means and the variance components of the random treatment effects; finally, confidence intervals are constructed by a parametric bootstrap procedure. The proposed method is evaluated by simulations and applications to 2 clinical trials.

摘要

采用荟萃分析方法评估替代终点的评估效果,是基于多项临床试验,评估治疗效果对替代终点的预测性,以及治疗效果对临床终点的预测性。在线性混合模型中,对治疗效果的相关性进行了定义和估计,后来根据具体情况扩展到二项或失效时间结局。在涵盖非正态结果的一般回归环境中,本文讨论了在替代终点评估中有用的几种指标。我们提出了一个统一的 3 步程序,用于评估在二项终点、生存时间结局或重复测量的环境中的这些指标。首先,通过估计方程方法确定估计的治疗效果的联合分布;其次,使用受限最大似然法估计随机治疗效果的均值和方差分量;最后,通过参数自举程序构建置信区间。该方法通过模拟和对 2 项临床试验的应用进行了评估。

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