Wathen J Kyle, Thall Peter F
Department of Biostatistics, University of Texas, M.D. Anderson Cancer Center, Box 447, 1515 Holcombe Boulevard, Houston, TX 77030, U.S.A.
Stat Med. 2008 Nov 29;27(27):5586-604. doi: 10.1002/sim.3381.
This article presents a new approach to the problem of deriving an optimal design for a randomized group sequential clinical trial based on right-censored event times. We are motivated by the fact that, if the proportional hazards assumption is not met, then a conventional design's actual power can differ substantially from its nominal value. We combine Bayesian decision theory, Bayesian model selection and forward simulation (FS) to obtain a group sequential procedure that maintains targeted false-positive rate and power, under a wide range of true event time distributions. At each interim analysis, the method adaptively chooses the most likely model and then applies the decision bounds that are optimal under the chosen model. A simulation study comparing this design with three conventional designs shows that, over a wide range of distributions, our proposed method performs at least as well as each conventional design, and in many cases it provides a much smaller trial.
本文提出了一种基于右删失事件时间推导随机分组序贯临床试验最优设计问题的新方法。我们的动机源于这样一个事实,即如果不满足比例风险假设,那么传统设计的实际功效可能与其名义值有很大差异。我们结合贝叶斯决策理论、贝叶斯模型选择和前向模拟(FS)来获得一种分组序贯程序,该程序在广泛的真实事件时间分布下保持目标假阳性率和功效。在每次期中分析时,该方法自适应地选择最可能的模型,然后应用在所选模型下最优的决策边界。一项将此设计与三种传统设计进行比较的模拟研究表明,在广泛的分布范围内,我们提出的方法至少与每种传统设计表现相当,并且在许多情况下它能提供规模小得多的试验。