Confirmatory adaptive designs with Bayesian decision tools for a targeted therapy in oncology

被引:131
作者
Brannath, Werner [2 ]
Zuber, Emmanuel [1 ]
Branson, Michael
Bretz, Frank [3 ]
Gallo, Paul [4 ]
Posch, Martin [2 ]
Racine-Poon, Amy
机构
[1] Novartis Pharma AG, Biostat & Stat Reporting Oncol, CH-4002 Basel, Switzerland
[2] Med Univ Vienna, Vienna, Austria
[3] Hannover Med Sch, Dept Biometry, D-30623 Hannover, Germany
[4] Novartis Pharmaceut, E Hanover, NJ USA
基金
奥地利科学基金会;
关键词
flexible design; sub-population selection; time to event data; predictive power; posterior probability; closure principle; group sequential design; biomarker; combination test; GROUP SEQUENTIAL DESIGNS; II/III CLINICAL-TRIALS; SAMPLE-SIZE; INTERIM; HYPOTHESES; INFERENCE; SELECTION;
D O I
10.1002/sim.3559
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to select a sensitive patient population may be crucial for the development of a targeted therapy. Identifying such a population with an acceptable level of confidence may lead to an inflation in development time and cost. We present all approach that allows to decrease these costs and to increase the reliability of the population selection. It is based on an actual adaptive phase II/III design and uses Bayesian decision tools to select the population of interest at an interim analysis. The primary endpoint is assumed to be the time to some event like e.g. progression. It is shown that the use of appropriately stratified logrank tests in the adaptive test procedture guarantees overall type I error control also when using information on patients that are censored at the adaptive interim analysis. The use of Bayesian decision tools for the population selection decision making is discussed. Simulations are presented to illustrate the operating characteristics of the study design relative to a more traditional development approach. Estimation of treatment effects is considered as well. Copyright (C) 2009 John Wiley & Sons. Ltd.
引用
收藏
页码:1445 / 1463
页数:19
相关论文
共 37 条
[31]   Sequential designs for phase III clinical trials incorporating treatment selection [J].
Stallard, N ;
Todd, S .
STATISTICS IN MEDICINE, 2003, 22 (05) :689-703
[32]   2-STAGE SELECTION AND TESTING DESIGNS FOR COMPARATIVE CLINICAL-TRIALS [J].
THALL, PF ;
SIMON, R ;
ELLENBERG, SS .
BIOMETRIKA, 1988, 75 (02) :303-310
[33]   A 2-STAGE DESIGN FOR CHOOSING AMONG SEVERAL EXPERIMENTAL TREATMENTS AND A CONTROL IN CLINICAL-TRIALS [J].
THALL, PF ;
SIMON, R ;
ELLENBERG, SS .
BIOMETRICS, 1989, 45 (02) :537-547
[34]   Biomarker as a classifier in pharmacogenomics clinical trials: a tribute to 30th anniversary of PSI [J].
Wang, Sue-Jane .
PHARMACEUTICAL STATISTICS, 2007, 6 (04) :283-296
[35]  
WASSMER G, 1999, STAT TESTVERFAHREN G
[36]   Planning and analyzing adaptive group sequential survival trials [J].
Wassmer, Gernot .
BIOMETRICAL JOURNAL, 2006, 48 (04) :714-729
[37]  
ZUBER E, 200605 U VIENNA DEP