Gu Xuemin, Chen Nan, Wei Caimiao, Liu Suyu, Papadimitrakopoulou Vassiliki A, Herbst Roy S, Lee J Jack
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Department of Thoracic, Head & Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Stat Biosci. 2016 Jun;8(1):99-128. doi: 10.1007/s12561-014-9124-2. Epub 2014 Dec 4.
We propose a Bayesian two-stage biomarker-based adaptive randomization (AR) design for the development of targeted agents. The design has three main goals: (1) to test the treatment efficacy, (2) to identify prognostic and predictive markers for the targeted agents, and (3) to provide better treatment for patients enrolled in the trial. To treat patients better, both stages are guided by the Bayesian AR based on the individual patient's biomarker profiles. The AR in the first stage is based on a known marker. A Go/No-Go decision can be made in the first stage by testing the overall treatment effects. If a Go decision is made at the end of the first stage, a two-step Bayesian lasso strategy will be implemented to select additional prognostic or predictive biomarkers to refine the AR in the second stage. We use simulations to demonstrate the good operating characteristics of the design, including the control of per-comparison type I and type II errors, high probability in selecting important markers, and treating more patients with more effective treatments. Bayesian adaptive designs allow for continuous learning. The designs are particularly suitable for the development of multiple targeted agents in the quest of personalized medicine. By estimating treatment effects and identifying relevant biomarkers, the information acquired from the interim data can be used to guide the choice of treatment for each individual patient enrolled in the trial in real time to achieve a better outcome. The design is being implemented in the BATTLE-2 trial in lung cancer at the MD Anderson Cancer Center.
我们提出了一种基于贝叶斯两阶段生物标志物的适应性随机化(AR)设计,用于靶向药物的研发。该设计有三个主要目标:(1)测试治疗效果;(2)识别靶向药物的预后和预测标志物;(3)为参与试验的患者提供更好的治疗。为了更好地治疗患者,两个阶段均由基于个体患者生物标志物特征的贝叶斯AR引导。第一阶段的AR基于已知标志物。通过测试总体治疗效果,可以在第一阶段做出继续/停止的决策。如果在第一阶段结束时做出继续的决策,将实施两步贝叶斯套索策略,以选择额外的预后或预测生物标志物,从而在第二阶段优化AR。我们通过模拟来证明该设计良好的操作特性,包括控制每次比较的I型和II型错误、选择重要标志物的高概率,以及用更有效的治疗方法治疗更多患者。贝叶斯适应性设计允许持续学习。这些设计特别适合于在追求个性化医疗的过程中开发多种靶向药物。通过估计治疗效果并识别相关生物标志物,从期中数据获得的信息可用于实时指导参与试验的每个个体患者的治疗选择,以实现更好的结果。该设计正在MD安德森癌症中心的肺癌BATTLE-2试验中实施。