Efficient targeted learning of heterogeneous treatment effects for multiple subgroups.

Journal: Biometrics
Published Date:

Abstract

In biomedical science, analyzing treatment effect heterogeneity plays an essential role in assisting personalized medicine. The main goals of analyzing treatment effect heterogeneity include estimating treatment effects in clinically relevant subgroups and predicting whether a patient subpopulation might benefit from a particular treatment. Conventional approaches often evaluate the subgroup treatment effects via parametric modeling and can thus be susceptible to model mis-specifications. In this paper, we take a model-free semiparametric perspective and aim to efficiently evaluate the heterogeneous treatment effects of multiple subgroups simultaneously under the one-step targeted maximum-likelihood estimation (TMLE) framework. When the number of subgroups is large, we further expand this path of research by looking at a variation of the one-step TMLE that is robust to the presence of small estimated propensity scores in finite samples. From our simulations, our method demonstrates substantial finite sample improvements compared to conventional methods. In a case study, our method unveils the potential treatment effect heterogeneity of rs12916-T allele (a proxy for statin usage) in decreasing Alzheimer's disease risk.

Authors

  • Waverly Wei
    Division of Biostatistics, University of California, Berkeley, California, USA.
  • Maya Petersen
  • Mark J van der Laan
    Division of Biostatistics, School of Public Health, University of California, Berkeley, CA, USA.
  • Zeyu Zheng
    Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang 110016, PR China.
  • Chong Wu
    School of Management, Harbin, China. Electronic address: wuchong@hit.edu.cn.
  • Jingshen Wang
    Division of Biostatistics, University of California, Berkeley, California, USA.