Subgroup identification in dose-finding trials via model-based recursive partitioning

被引:14
|
作者
Thomas, Marius [1 ]
Bornkamp, Bjoern [1 ]
Seibold, Heidi [2 ]
机构
[1] Novartis Pharma AG, CH-4002 Basel, Switzerland
[2] Univ Zurich, Hirschengraben 84, CH-8001 Zurich, Switzerland
关键词
dose estimation; nonlinear models; personalized medicine; regression trees; CLINICAL-TRIALS;
D O I
10.1002/sim.7594
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
An important task in early-phase drug development is to identify patients, which respond better or worse to an experimental treatment. While a variety of different subgroup identification methods have been developed for the situation of randomized clinical trials that study an experimental treatment and control, much less work has been done in the situation when patients are randomized to different dose groups. In this article, we propose new strategies to perform subgroup analyses in dose-finding trials and discuss the challenges, which arise in this new setting. We consider model-based recursive partitioning, which has recently been applied to subgroup identification in 2-arm trials, as a promising method to tackle these challenges and assess its viability using a real trial example and simulations. Our results show that model-based recursive partitioning can be used to identify subgroups of patients with different dose-response curves and improves estimation of treatment effects and minimum effective doses compared to models ignoring possible subgroups, when heterogeneity among patients is present.
引用
收藏
页码:1608 / 1624
页数:17
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