Optimal planning of adaptive two-stage designs

被引:9
|
作者
Pilz, Maximilian [1 ]
Kunzmann, Kevin [2 ]
Herrmann, Carolin [3 ,4 ,5 ]
Rauch, Geraldine [3 ,4 ,5 ]
Kieser, Meinhard [1 ]
机构
[1] Heidelberg Univ, Univ Med Ctr, Inst Med Biometry & Informat, Neuenheimer Feld 130-3, D-69120 Heidelberg, Germany
[2] Univ Cambridge, Cambridge Inst Publ Hlth, MRC Biostat Unit, Cambridge, England
[3] Charite Univ Med Berlin, Berlin, Germany
[4] Free Univ Berlin, Berlin, Germany
[5] Humboldt Univ, Inst Biometry & Clin Epidemiol, Berlin, Germany
关键词
adaptive design; clinical trial; optimal design; sample size calculation; SAMPLE-SIZE; CLINICAL-TRIALS;
D O I
10.1002/sim.8953
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adaptive designs are playing an increasingly important role in the planning of clinical trials. While there exists various research on the optimal determination of a two-stage design, non-optimal versions still are frequently applied in clinical research. In this article, we strive to motivate the application of optimal adaptive designs and give guidance on how to determine them. It is demonstrated that optimizing a trial design with respect to particular objective criteria can have a substantial benefit over the application of conventional adaptive sample size recalculation rules. Furthermore, we show that in many practical situations, optimal group-sequential designs show an almost negligible performance loss compared to optimal adaptive designs. Finally, we illustrate how optimal designs can be tailored to specific operational requirements by customizing the underlying optimization problem.
引用
收藏
页码:3196 / 3213
页数:18
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