Comparing Four Methods for Estimating Tree-Based Treatment Regimes

被引:11
作者
Sies, Aniek [1 ]
Van Mechelen, Iven [1 ]
机构
[1] Katholieke Univ Leuven, Fac Psychol & Educ Sci, Tiensestr 102,Box 3713, B-3000 Leuven, Belgium
基金
比利时弗兰德研究基金会;
关键词
treatment regime; subgroup analysis; recursive partitioning; personalized medicine; decision tree; SUBGROUP IDENTIFICATION; TRIALS;
D O I
10.1515/ijb-2016-0068
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
When multiple treatment alternatives are available for a certain psychological or medical problem, an important challenge is to find an optimal treatment regime, which specifies for each patient the most effective treatment alternative given his or her pattern of pretreatment characteristics. The focus of this paper is on tree-based treatment regimes, which link an optimal treatment alternative to each leaf of a tree; as such they provide an insightful representation of the decision structure underlying the regime. This paper compares the absolute and relative performance of four methods for estimating regimes of that sort (viz., Interaction Trees, Model-based Recursive Partitioning, an approach developed by Zhang et al. and Qualitative Interaction Trees) in an extensive simulation study. The evaluation criteria were, on the one hand, the expected outcome if the entire population would be subjected to the treatment regime resulting from each method under study and the proportion of clients assigned to the truly best treatment alternative, and, on the other hand, the Type I and Type II error probabilities of each method. The method of Zhang et al. was superior regarding the first two outcome measures and the Type II error probabilities, but performed worst in some conditions of the simulation study regarding Type I error probabilities.
引用
收藏
页数:20
相关论文
共 52 条
[1]  
[Anonymous], 2010, The rpart package
[2]   Subgroup analysis and other (mis)uses of baseline data in clinical trials [J].
Assmann, SF ;
Pocock, SJ ;
Enos, LE ;
Kasten, LE .
LANCET, 2000, 355 (9209) :1064-1069
[3]   Doubly robust estimation in missing data and causal inference models [J].
Bang, H .
BIOMETRICS, 2005, 61 (04) :962-972
[4]   A BAYESIAN APPROACH TO SUBGROUP IDENTIFICATION [J].
Berger, James O. ;
Wang, Xiaojing ;
Shen, Lei .
JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2014, 24 (01) :110-129
[5]   SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation [J].
Blewitt, Marnie E. ;
Gendrel, Anne-Valerie ;
Pang, Zhenyi ;
Sparrow, Duncan B. ;
Whitelaw, Nadia ;
Craig, Jeffrey M. ;
Apedaile, Anwyn ;
Hilton, Douglas J. ;
Dunwoodie, Sally L. ;
Brockdorff, Neil ;
Kay, Graham F. ;
Whitelaw, Emma .
NATURE GENETICS, 2008, 40 (05) :663-669
[6]   A Generalized Estimator of the Attributable Benefit of an Optimal Treatment Regime [J].
Brinkley, Jason ;
Tsiatis, Anastasios ;
Anstrom, Kevin J. .
BIOMETRICS, 2010, 66 (02) :512-522
[7]  
Brookes S T, 2001, Health Technol Assess, V5, P1
[9]   Motivational interviewing to improve treatment engagement and outcome in individuals seeking treatment for substance abuse: A multisite effectiveness study [J].
Carroll, KM ;
Ball, SA ;
Nich, C ;
Martino, S ;
Frankforter, TL ;
Farentinos, C ;
Kunkel, LE ;
Mikulich-Gilbertson, SK ;
Morgenstern, J ;
Obert, JL ;
Polcin, D ;
Snead, N ;
Woody, GE .
DRUG AND ALCOHOL DEPENDENCE, 2006, 81 (03) :301-312
[10]  
Cohen J, 2013, Statistical power analysis for the behavioral sciences, DOI [10.4324/9780203771587, DOI 10.4324/9780203771587]