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使用未知形状参数的 Weibull 分布对具有时间事件终点的单臂临床试验进行样本量重估和贝叶斯预测概率。

Sample size reestimation and Bayesian predictive probability for single-arm clinical trials with a time-to-event endpoint using Weibull distribution with unknown shape parameter.

机构信息

Biostatistics and Research Decision Sciences, Merck & Co, Inc, North Wales, Pennsylvania, United States.

Department of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States.

出版信息

J Biopharm Stat. 2024 Jul 3;34(4):469-487. doi: 10.1080/10543406.2023.2234998. Epub 2023 Aug 6.

Abstract

This manuscript consists of two topics. Firstly, we explore the utility of internal pilot study (IPS) approach for reestimating sample size at an interim stage when a reliable estimate of the nuisance shape parameter of the Weibull distribution for modeling survival data is unavailable during the planning phase of a study. Although IPS approach can help rescue the study power, it is noted that the adjusted sample size can be as much as twice the initially planned sample size, which may put substantial practical constraints to continue the study. Secondly, we discuss Bayesian predictive probability for conducting interim analyses to obtain preliminary evidence of efficacy or futility of an experimental treatment warranting early termination of a clinical trial. In the context of single-arm clinical trials with time-to-event endpoints following Weibull distribution, we present the calculation of the Bayesian predictive probability when the shape parameter of the Weibull distribution is unknown. Based on the data accumulated at the interim, we propose two approaches which rely on the posterior mode or the entire posterior distribution of the shape parameter. To account for uncertainty in the shape parameter, it is recommended to incorporate its entire posterior distribution in our calculation.

摘要

本文稿由两个主题组成。首先,我们探索了内部试点研究(IPS)方法的实用性,即在研究规划阶段无法获得 Weibull 分布形状参数的可靠估计值时,在中期重新估计生存数据模型的样本量。虽然 IPS 方法可以帮助挽救研究的效力,但需要注意的是,调整后的样本量可能会达到最初计划样本量的两倍,这可能会对继续研究造成实质性的实际限制。其次,我们讨论了贝叶斯预测概率在进行中期分析中的应用,以获得早期试验治疗效果或无效的初步证据,从而有理由提前终止临床试验。在针对 Weibull 分布的时间相关终点的单臂临床试验中,我们介绍了当 Weibull 分布的形状参数未知时贝叶斯预测概率的计算方法。基于中期积累的数据,我们提出了两种依赖于形状参数后验模式或整个后验分布的方法。为了考虑形状参数的不确定性,建议在我们的计算中纳入其整个后验分布。

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