Chen Ming-Hui, Ibrahim Joseph G, Lam Peter, Yu Alan, Zhang Yuanye
Department of Statistics, University of Connecticut, 215 Glenbrook Road, Storrs, Connecticut 06269, USA.
Biometrics. 2011 Sep;67(3):1163-70. doi: 10.1111/j.1541-0420.2011.01561.x. Epub 2011 Mar 1.
We develop a new Bayesian approach of sample size determination (SSD) for the design of noninferiority clinical trials. We extend the fitting and sampling priors of Wang and Gelfand (2002, Statistical Science 17, 193-208) to Bayesian SSD with a focus on controlling the type I error and power. Historical data are incorporated via a hierarchical modeling approach as well as the power prior approach of Ibrahim and Chen (2000, Statistical Science 15, 46-60). Various properties of the proposed Bayesian SSD methodology are examined and a simulation-based computational algorithm is developed. The proposed methodology is applied to the design of a noninferiority medical device clinical trial with historical data from previous trials.
我们开发了一种用于非劣效性临床试验设计的新的贝叶斯样本量确定(SSD)方法。我们将Wang和Gelfand(2002年,《统计科学》17卷,193 - 208页)的拟合和抽样先验方法扩展到贝叶斯SSD,重点是控制I型错误和检验效能。通过分层建模方法以及Ibrahim和Chen(2000年,《统计科学》15卷,46 - 60页)的效能先验方法纳入历史数据。研究了所提出的贝叶斯SSD方法的各种性质,并开发了一种基于模拟的计算算法。所提出的方法应用于一个具有先前试验历史数据的非劣效性医疗器械临床试验的设计。