首页 | 本学科首页   官方微博 | 高级检索  
     


Evaluation of biomarkers for treatment selection using individual participant data from multiple clinical trials
Authors:Chaeryon Kang,Holly Janes,Parvin Tajik,Henk Groen,Ben Mol,Corine Koopmans,Kim Broekhuijsen,Eva Zwertbroek,Maria van   Pampus,Maureen Franssen
Affiliation:1. Department of Biostatistics, University of Pittsburgh, Pittsburgh, U.S.A;2. Vaccine and Infectious Disease Division and Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, U.S.A.;3. Department of Clinical Epidemiology & Biostatistics, University of Amsterdam, Amsterdam, The Netherlands;4. Department of Pathology, Academic Medical Center, Amsterdam, Netherlands;5. Department of Epidemiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands;6. Department of Obstetrics and Gynaecology, School of Medicine, Monash University, Melbourne, Australia;7. Department of Obstetrics and Gynecology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands;8. Department of Obstetrics and Gynecology, Onze Lieve Vrouwe Gasthuis, Amsterdam, Netherlands
Abstract:Biomarkers that predict treatment effects may be used to guide treatment decisions, thus improving patient outcomes. A meta‐analysis of individual participant data (IPD) is potentially more powerful than a single‐study data analysis in evaluating markers for treatment selection. Our study was motivated by the IPD that were collected from 2 randomized controlled trials of hypertension and preeclampsia among pregnant women to evaluate the effect of labor induction over expectant management of the pregnancy in preventing progression to severe maternal disease. The existing literature on statistical methods for biomarker evaluation in IPD meta‐analysis have evaluated a marker's performance in terms of its ability to predict risk of disease outcome, which do not directly apply to the treatment selection problem. In this study, we propose a statistical framework for evaluating a marker for treatment selection given IPD from a small number of individual clinical trials. We derive marker‐based treatment rules by minimizing the average expected outcome across studies. The application of the proposed methods to the IPD from 2 studies in women with hypertension in pregnancy is presented.
Keywords:HYPITAT trials  individual participant data  randomized clinical trial  treatment selection biomarker
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号