首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Bayesian monitoring of clinical trials with failure-time endpoints
Authors:Rosner Gary L
Institution:Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, The University of Texas, 1515 Holcombe Boulevard, Unit 447, Houston, Texas 77030, USA. glr@odin.mdacc.tmc.edu
Abstract:This article presents an aid for monitoring clinical trials with failure-time endpoints based on the Bayesian nonparametric analyses of the data. The posterior distribution is a mixture of Dirichlet processes in the presence of censoring if one assumes a Dirichlet process prior for the survival distribution. Using Gibbs sampling, one can generate random samples from the posterior distribution. With samples from the posterior distributions of treatment-specific survival curves, one can evaluate the current evidence in favor of stopping or continuing the trial based on summary statistics of these survival curves. Because the method is nonparametric, it can easily be used, for example, in situations where hazards cross or are suspected to cross and where relevant clinical decisions might be based on estimating when the integral between the curves might be expected to become positive and in favor of the new but toxic therapy. An example based on an actual trial illustrates the method.
Keywords:Clinical trials  Dirichlet process  Gibbs sampling  Survival analysis
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号