Zang Yong, Guo Beibei
1 Department of Mathematical Sciences, Florida Atlantic University, Boca Raton, FL, USA.
2 Department of Experimental Statistics, Louisiana State University, Baton Rouge, LA, USA.
Stat Methods Med Res. 2018 Jan;27(1):35-47. doi: 10.1177/0962280215618429. Epub 2015 Nov 26.
The enrichment design is an important clinical trial design to detect the treatment effect of the molecularly targeted agent (MTA) in personalized medicine. Under this design, patients are stratified into marker-positive and marker-negative subgroups based on their biomarker statuses and only the marker-positive patients are enrolled into the trial and randomized to receive either the MTA or a standard treatment. As the biomarker plays a key role in determining the enrollment of the trial, a misclassification of the biomarker can induce substantial bias, undermine the integrity of the trial, and seriously affect the treatment evaluation. In this paper, we propose a two-stage optimal enrichment design that utilizes the surrogate marker to correct for the biomarker misclassification. The proposed design is optimal in the sense that it maximizes the probability of correctly classifying each patient's biomarker status based on the surrogate marker information. In addition, after analytically deriving the bias caused by the biomarker misclassification, we develop a likelihood ratio test based on the EM algorithm to correct for such bias. We conduct comprehensive simulation studies to investigate the operating characteristics of the optimal design and the results confirm the desirable performance of the proposed design.
富集设计是个性化医疗中检测分子靶向药物(MTA)治疗效果的重要临床试验设计。在此设计下,患者根据其生物标志物状态被分层为标志物阳性和标志物阴性亚组,只有标志物阳性患者被纳入试验并随机接受MTA或标准治疗。由于生物标志物在确定试验入组方面起着关键作用,生物标志物的错误分类会导致严重偏差,破坏试验的完整性,并严重影响治疗评估。在本文中,我们提出了一种两阶段最优富集设计,该设计利用替代标志物来纠正生物标志物的错误分类。所提出的设计是最优的,因为它基于替代标志物信息最大化正确分类每个患者生物标志物状态的概率。此外,在分析得出生物标志物错误分类所导致的偏差后,我们基于期望最大化(EM)算法开发了一种似然比检验来纠正这种偏差。我们进行了全面的模拟研究以调查最优设计的操作特性,结果证实了所提出设计的理想性能。