Xia Fang, George Stephen L, Ning Jing, Li Liang, Huang Xuelin
Department of Biostatistics, The University of Texas MD Anderson Cancer Center.
Department of Biostatistics and Bioinformatics, Duke University School of Medicine.
J Appl Stat. 2021;48(6):1091-1110. doi: 10.1080/02664763.2020.1757048. Epub 2020 Apr 27.
Clinical trials in the era of precision cancer medicine aim to identify and validate biomarker signatures which can guide the assignment of individually optimal treatments to patients. In this article, we propose a group sequential randomized phase II design, which updates the biomarker signature as the trial goes on, utilizes enrichment strategies for patient selection, and uses Bayesian response-adaptive randomization for treatment assignment. To evaluate the performance of the new design, in addition to the commonly considered criteria of type I error and power, we propose four new criteria measuring the benefits and losses for individuals both inside and outside of the clinical trial. Compared with designs with equal randomization, the proposed design gives trial participants a better chance to receive their personalized optimal treatments and thus results in a higher response rate on the trial. This design increases the chance to discover a successful new drug by an adaptive enrichment strategy, i.e., identification and selective enrollment of a subset of patients who are sensitive to the experimental therapies. Simulation studies demonstrate these advantages of the proposed design. It is illustrated by an example based on an actual clinical trial in non-small-cell lung cancer.
精准癌症医学时代的临床试验旨在识别和验证生物标志物特征,以指导为患者分配个体化的最佳治疗方案。在本文中,我们提出了一种成组序贯随机II期设计,该设计在试验进行过程中更新生物标志物特征,采用富集策略进行患者选择,并使用贝叶斯反应自适应随机化进行治疗分配。为了评估新设计的性能,除了常用的I型错误和检验效能标准外,我们还提出了四个新的标准,用于衡量临床试验内外个体的收益和损失。与等随机化设计相比,所提出的设计使试验参与者有更好的机会接受个性化的最佳治疗,从而在试验中获得更高的缓解率。这种设计通过自适应富集策略增加了发现成功新药的机会,即识别和选择性招募对实验性治疗敏感的患者亚组。模拟研究证明了所提出设计的这些优势。通过一个基于非小细胞肺癌实际临床试验的例子进行了说明。