Sample size calculation for randomized selection trials with a time-to-event endpoint and a margin of practical equivalence

被引:2
|
作者
Dehbi, Hakim-Moulay [1 ]
Embleton-Thirsk, Andrew [1 ]
McCaw, Zachary Ryan [2 ]
机构
[1] UCL, Comprehens Clin Trials Unit, 90 High Holborn 2nd Floor, London WC1V 6LJ, England
[2] Insitro, South San Francisco, CA USA
关键词
early phase trials; randomization; sample size calculation; selection trials; PHASE-II; CHEMORADIATION; SURVIVAL;
D O I
10.1002/sim.9490
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Selection trials are used to compare potentially active experimental treatments without a control arm. While sample size calculation methods exist for binary endpoints, no such methods are available for time-to-event endpoints, even though these are ubiquitous in clinical trials. Recent selection trials have begun using progression-free survival as their primary endpoint, but have dichotomized it at a specific time point for sample size calculation and analysis. This changes the clinical question and may reduce power to detect a difference between the arms. In this article, we develop the theory for sample size calculation in selection trials where the time-to-event endpoint is assumed to follow an exponential or Weilbull distribution. We provide a free web application for sample size calculation, as well as an R package, that researchers can use in the design of their studies.
引用
收藏
页码:4022 / 4033
页数:12
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