Stepwise two-stage sample size adaptation

被引:3
作者
Wan, Hong [1 ]
Ellenberg, Susan S. [2 ]
Anderson, Keaven M. [3 ]
机构
[1] Shire, Wayne, PA 19087 USA
[2] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[3] Merck Res Labs, Clin Biostat & Res Decis Sci, N Wales, PA 19454 USA
关键词
sample size reestimation; adaptive design; optimal design; CLINICAL-TRIAL DESIGNS;
D O I
10.1002/sim.6311
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several adaptive design methods have been proposed to reestimate sample size using the observed treatment effect after an initial stage of a clinical trial while preserving the overall type I error at the time of the final analysis. One unfortunate property of the algorithms used in some methods is that they can be inverted to reveal the exact treatment effect at the interim analysis. We propose using a step function with an inverted U-shape of observed treatment difference for sample size reestimation to lessen the information on treatment effect revealed. This will be referred to as stepwise two-stage sample size adaptation. This method applies calculation methods used for group sequential designs. We minimize expected sample size among a class of these designs and compare efficiency with the fully optimized two-stage design, optimal two-stage group sequential design, and designs based on promising conditional power. The trade-off between efficiency versus the improved blinding of the interim treatment effect will be discussed. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 18 条
[1]   Optimal spending functions for asymmetric group sequential designs [J].
Anderson, Keaven M. .
BIOMETRICAL JOURNAL, 2007, 49 (03) :337-345
[2]  
Andersons KM, 2004, OPTIMAL ADAPTIVE VS
[3]   Optimal asymmetric one-sided group sequential tests [J].
Barber, S ;
Jennison, C .
BIOMETRIKA, 2002, 89 (01) :49-60
[4]   Increasing the sample size when the unblinded interim result is promising [J].
Chen, YHJ ;
DeMets, DL ;
Lan, KKG .
STATISTICS IN MEDICINE, 2004, 23 (07) :1023-1038
[5]   Sample size reestimation: A review and recommendations [J].
Chuang-Stein, Christy ;
Anderson, Keaven ;
Gallo, Paul ;
Collins, Sylva .
DRUG INFORMATION JOURNAL, 2006, 40 (04) :475-484
[6]   Modification of sample size in group sequential clinical trials [J].
Cui, L ;
Hung, HMJ ;
Wang, SJ .
BIOMETRICS, 1999, 55 (03) :853-857
[7]   Papers from the 2004 Harvard-MIT Division of Health Science and Technology Workshop, "Adaptive Clinical Trial Designs: Ready for Prime Time?" - Preface [J].
Ellenberg, Susan S. ;
Golub, Howard ;
Metha, Cyrus ;
D'Agostino, Ralph .
STATISTICS IN MEDICINE, 2006, 25 (19) :3229-3230
[8]   Sample Size Re-Estimation for Adaptive Sequential Design in Clinical Trials [J].
Gao, Ping ;
Ware, James H. ;
Mehta, Cyrus .
JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2008, 18 (06) :1184-1196
[9]   Mid-course sample size modification in clinical trials based on the observed treatment effect [J].
Jennison, C ;
Turnbull, BW .
STATISTICS IN MEDICINE, 2003, 22 (06) :971-993
[10]  
Jennisons C, 2000, GROUP SEQUENTIAL MET