Admissible two-stage designs for phase II cancer clinical trials

被引:132
作者
Jung, SH
Lee, T
Kim, K
George, SL
机构
[1] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC 27710 USA
[2] SAS Inst Inc, Cary, NC USA
[3] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53706 USA
关键词
Bayes design; compromise design; minimax design; optimal design; sequential design;
D O I
10.1002/sim.1600
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In a typical two-stage design for a phase 11 cancer clinical trial for efficacy screening of cytotoxic agents, a fixed number of patients are initially enrolled and treated. The trial may be terminated for lack of efficacy if the observed number of tumour responses after the first stage is too small, thus avoiding treatment of patient with inefficacious regimen. Otherwise, an additional fixed number of patients are enrolled and treated to accumulate additional information on efficacy as well as safety. The minimax and the so-called 'optimal' designs by Simon have been widely used, and other designs have largely been ignored in the past for such two-stage cancer clinical trials. Recently Jung et al. proposed a graphical method to search for compromise designs with features more favourable than either the minimax or the optimal design. In this paper, we develop a family of two-stage designs that are admissible according to a Bayesian decision-theoretic criterion based on an ethically justifiable loss function. We show that the admissible designs include as special cases the Simon's minimax and the optimal designs as well as the compromise designs introduced by Jung et al. We also present a Java program to search for admissible designs that are compromises between the minimax and the optimal designs. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:561 / 569
页数:9
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