Comment: Inference after covariate-adaptive randomisation: aspects of methodology and theory

IF 0.7 Q3 STATISTICS & PROBABILITY
Bingkai Wang, Ryoko Susukida, R. Mojtabai, M. Amin-Esmaeili, Michael Rosenblum
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引用次数: 0

Abstract

We thank the editor for the opportunity to write this commentary on the paper by Jun Shao. The author’s paper gives an excellent review of methods developed for statistical inference when considering covariateadaptive, randomised trial designs. We would like to mention how the results from our paper (Wang et al., 2020) fit into those described by Jun Shao. Our paper focused on stratified permuted block randomisation (Zelen, 1974) and also biased coin randomisation (Efron, 1971), which are categorised as Type 1 randomisation schemes in the author’s paper. According to a survey by Lin et al. (2015) on 224 randomised clinical trials published in leading medical journals in 2014, stratified permuted block randomization was used by 70% of trials. Our goal is to improve precision of statistical inference by combining covariate-adaptive design and covariate adjustment, while providing robustness to model misspecification. In Section 6 of the author’s paper, the same goal was discussed and a linear model of potential outcomes given covariates was considered. Our results generalise those given for linearmodel-based estimators to all M-estimators (under regularity conditions), which covers many estimators used to analyse data from randomised clinical trials. Examples of M-estimators include estimators based on logistic regression (Moore & van der Laan, 2009), inverse probability weighting (Robins et al., 1994), the doubly-robust weighted-least-squares estimator (Robins et al., 2007), the augmented inverse probability weighted estimator (Robins et al., 1994; Scharfstein et al., 1999), and targeted maximum likelihood estimators (TMLE) that converge in 1-step (van der Laan&Gruber, 2012). Our results are able to handle covariate adjustment, various outcome types, repeated measures outcomes and missing outcome data under the missing at random assumption. Using data from three completed trials of substance use disorder treatments, we estimated that the precision gained due to stratified permuted block randomisation and covariate adjustment ranged from 1% to 36%. Another contribution of our paper is to prove the consistency and asymptotic normality of the KaplanMeier estimator under stratified randomization. Its asymptotic variance was also derived. We conjecture that this result can be generalised to cover covariate-adjusted estimators for the survival function, such as estimators by Lu and Tsiatis (2011); Zhang (2015).
评论:协变量自适应随机化后的推理:方法论和理论方面
我们感谢编辑给邵军的这篇评论文章的机会。作者的论文对在考虑协变量自适应随机试验设计时为统计推断开发的方法进行了极好的综述。我们想提及的是,我们的论文(Wang et al.,2020)的结果如何与邵军描述的结果相吻合。我们的论文集中于分层排列块随机化(Zelen,1974)和有偏硬币随机化(Efron,1971),在作者的论文中被归类为1型随机化方案。根据Lin等人(2015)对2014年发表在主流医学期刊上的224项随机临床试验的调查,70%的试验使用了分层排列块随机化。我们的目标是通过将协变量自适应设计和协变量调整相结合来提高统计推断的精度,同时提供对模型错误指定的鲁棒性。在作者论文的第6节中,讨论了相同的目标,并考虑了给定协变量的潜在结果的线性模型。我们的结果将基于线性模型的估计量推广到所有M-估计量(在正则性条件下),其中包括用于分析随机临床试验数据的许多估计量。M-估计量的例子包括基于逻辑回归的估计量(Moore&van der Laan,2009)、逆概率加权(Robins等人,1994)、双稳健加权最小二乘估计量(Robins et al.,2007)、增强逆概率加权估计量(Robins等人,1994;Scharfstein等人,1999),以及在1步中收敛的目标最大似然估计量(TMLE)(van der Laan&Gruber,2012)。我们的结果能够处理随机缺失假设下的协变量调整、各种结果类型、重复测量结果和缺失结果数据。使用三项已完成的药物使用障碍治疗试验的数据,我们估计,由于分层排列块随机化和协变量调整而获得的精度在1%至36%之间。本文的另一个贡献是证明了KaplanMeier估计量在分层随机化下的一致性和渐近正态性。推导了它的渐近方差。我们猜想这个结果可以推广到覆盖生存函数的协变量调整估计量,例如Lu和Tsiatis(2011)的估计量;张(2015)。
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
CiteScore
0.90
自引率
20.00%
发文量
21
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