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.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Muhammad Waleed, Jianghua He, Milind A Phadnis
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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.

使用具有未知形状参数的 Weibull 分布,对具有时间到事件终点的单臂临床试验进行样本量再估计和贝叶斯预测概率。
本手稿包括两个主题。首先,我们探讨了内部试验研究(IPS)方法的实用性,当在研究计划阶段无法获得用于生存数据建模的 Weibull 分布的滋扰形状参数的可靠估计值时,可以在中期阶段重新估计样本量。虽然 IPS 方法可以帮助挽救研究功率,但我们注意到调整后的样本量可能是最初计划样本量的两倍,这可能会对继续研究造成很大的实际限制。其次,我们讨论了进行中期分析的贝叶斯预测概率,以获得实验治疗的疗效或无效的初步证据,从而提前终止临床试验。在单臂临床试验中,事件终点的时间服从于 Weibull 分布,当 Weibull 分布的形状参数未知时,我们将介绍贝叶斯预测概率的计算方法。根据中期积累的数据,我们提出了依赖于形状参数的后验模式或整个后验分布的两种方法。为了考虑形状参数的不确定性,我们建议将其整个后验分布纳入计算。
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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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