Biostatistics and Bioinformatics Shared Resource Facility, Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA.
Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Pharm Stat. 2021 Nov;20(6):1235-1248. doi: 10.1002/pst.2143. Epub 2021 Jun 4.
For the cancer clinical trials with immunotherapy and molecularly targeted therapy, time-to-event endpoint is often a desired endpoint. In this paper, we present an event-driven approach for Bayesian one-stage and two-stage single-arm phase II trial designs. Two versions of Bayesian one-stage designs were proposed with executable algorithms and meanwhile, we also develop theoretical relationships between the frequentist and Bayesian designs. These findings help investigators who want to design a trial using Bayesian approach have an explicit understanding of how the frequentist properties can be achieved. Moreover, the proposed Bayesian designs using the exact posterior distributions accommodate the single-arm phase II trials with small sample sizes. We also proposed an optimal two-stage approach, which can be regarded as an extension of Simon's two-stage design with the time-to-event endpoint. Comprehensive simulations were conducted to explore the frequentist properties of the proposed Bayesian designs and an R package BayesDesign can be assessed via R CRAN for convenient use of the proposed methods.
对于包含免疫疗法和分子靶向治疗的癌症临床试验,事件时间终点通常是理想的终点。在本文中,我们提出了一种基于事件驱动的贝叶斯单阶段和两阶段单臂二期临床试验设计方法。提出了两种版本的贝叶斯单阶段设计,并提供了可执行的算法,同时还建立了贝叶斯和频率设计之间的理论关系。这些发现有助于那些希望使用贝叶斯方法设计试验的研究人员清楚地了解如何实现频率设计的性质。此外,使用精确后验分布的建议贝叶斯设计适用于样本量较小的单臂二期试验。我们还提出了一种最优的两阶段方法,它可以被视为具有事件时间终点的 Simon 两阶段设计的扩展。通过综合模拟研究,探索了所提出的贝叶斯设计的频率性质,并可以通过 R CRAN 评估 R 包 BayesDesign,以便方便地使用所提出的方法。