Randomization-based covariance analysis for hypothesis testing of treatment comparisons based on restricted mean survival time with categorized time-to-event data.

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Taylor J Krajewski, Gary G Koch
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Abstract

This paper introduces randomization-based analysis of covariance (RB-ANCOVA) for hypothesis testing of restricted mean survival time (RMST) differences between two randomized treatments in trials with categorized time-to-event data. RMST treatment differences over a prespecified time period are clinically meaningful and avoid assumptions like proportional hazards. The proposed method tests the strong null hypothesis that each participant's time-to-event would remain unchanged regardless of treatment assignment. Covariate adjustment is achieved by constraining baseline covariate means to be equal across arms, which reduces variance. The follow-up period is partitioned into mutually exclusive intervals, and RMST is approximated as the area under the survival curve. Under the strong null hypothesis, the joint asymptotic covariance structure of RMST and covariate means is known and used to construct a chi-squared test statistic for the covariate-adjusted RMST difference. The method accommodates stratified trial designs and supports hypothesis testing over single or several time intervals, enabling testing within internal intervals. The difference in RMSTs over an interval can be divided by its length to yield an average survival rate difference. Additionally, the approach allows the computation of essentially exact p-values via re-randomization. We illustrate the method with data from a randomized, placebo-controlled trial evaluating a test treatment for amyotrophic lateral sclerosis. This method provides a hypothesis testing approach for RMST treatment differences that leverages RB-ANCOVA to adjust for their correlations with baseline covariate differences. Under the strong null hypothesis, it enables hypothesis testing with clear control of Type I error and reduced variance without relying on model-based assumptions.

基于限制平均生存时间和分类事件时间数据的治疗比较的随机化协方差分析的假设检验。
本文引入基于随机化的协方差分析(RB-ANCOVA),对两种随机治疗的限制性平均生存时间(RMST)差异进行假设检验。在预先规定的时间段内,RMST治疗差异具有临床意义,并避免了比例风险等假设。所提出的方法检验了强零假设,即无论治疗分配如何,每个参与者到事件的时间将保持不变。协变量调整是通过约束基线协变量均值在各臂之间相等来实现的,这样可以减少方差。随访期被划分为相互排斥的间隔,RMST近似为生存曲线下的面积。在强零假设下,已知RMST与协变量均值的联合渐近协方差结构,并用于构建协变量调整后RMST差的卡方检验统计量。该方法适用于分层试验设计,并支持在单个或多个时间间隔内进行假设检验,从而可以在内部时间间隔内进行检验。rmst在一段时间内的差异可以除以其长度,从而得到平均存活率差异。此外,该方法允许通过重新随机化计算本质上精确的p值。我们用一项随机、安慰剂对照试验的数据来说明这种方法,该试验评估了肌萎缩性侧索硬化症的试验治疗。该方法为RMST治疗差异提供了一种假设检验方法,该方法利用RB-ANCOVA来调整其与基线协变量差异的相关性。在强零假设下,假设检验可以明确控制I型误差,减少方差,而不依赖于基于模型的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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