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A general statistical framework for subgroup identification and comparative treatment scoring

Author

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  • Shuai Chen
  • Lu Tian
  • Tianxi Cai
  • Menggang Yu

Abstract

Many statistical methods have recently been developed for identifying subgroups of patients who may benefit from different available treatments. Compared with the traditional outcome‐modeling approaches, these methods focus on modeling interactions between the treatments and covariates while by‐pass or minimize modeling the main effects of covariates because the subgroup identification only depends on the sign of the interaction. However, these methods are scattered and often narrow in scope. In this article, we propose a general framework, by weighting and A‐learning, for subgroup identification in both randomized clinical trials and observational studies. Our framework involves minimum modeling for the relationship between the outcome and covariates pertinent to the subgroup identification. Under the proposed framework, we may also estimate the magnitude of the interaction, which leads to the construction of scoring system measuring the individualized treatment effect. The proposed methods are quite flexible and include many recently proposed estimators as special cases. As a result, some estimators originally proposed for randomized clinical trials can be extended to observational studies, and procedures based on the weighting method can be converted to an A‐learning method and vice versa. Our approaches also allow straightforward incorporation of regularization methods for high‐dimensional data, as well as possible efficiency augmentation and generalization to multiple treatments. We examine the empirical performance of several procedures belonging to the proposed framework through extensive numerical studies.

Suggested Citation

  • Shuai Chen & Lu Tian & Tianxi Cai & Menggang Yu, 2017. "A general statistical framework for subgroup identification and comparative treatment scoring," Biometrics, The International Biometric Society, vol. 73(4), pages 1199-1209, December.
  • Handle: RePEc:bla:biomet:v:73:y:2017:i:4:p:1199-1209
    DOI: 10.1111/biom.12676
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    References listed on IDEAS

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    Cited by:

    1. Riccardo Di Francesco, 2022. "Aggregation Trees," CEIS Research Paper 546, Tor Vergata University, CEIS, revised 20 Nov 2023.
    2. Lechner, Michael, 2018. "Modified Causal Forests for Estimating Heterogeneous Causal Effects," IZA Discussion Papers 12040, Institute of Labor Economics (IZA).
    3. Zhilan Lou & Jun Shao & Menggang Yu, 2018. "Optimal treatment assignment to maximize expected outcome with multiple treatments," Biometrics, The International Biometric Society, vol. 74(2), pages 506-516, June.
    4. Buhl-Wiggers, Julie & Kerwin, Jason T. & Muñoz-Morales, Juan & Smith, Jeffrey & Thornton, Rebecca, 2024. "Some children left behind: Variation in the effects of an educational intervention," Journal of Econometrics, Elsevier, vol. 243(1).
    5. Anthony Strittmatter, 2018. "What Is the Value Added by Using Causal Machine Learning Methods in a Welfare Experiment Evaluation?," Papers 1812.06533, arXiv.org, revised Dec 2021.
    6. Weibin Mo & Yufeng Liu, 2022. "Efficient learning of optimal individualized treatment rules for heteroscedastic or misspecified treatment‐free effect models," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 84(2), pages 440-472, April.
    7. Michael Lechner & Jana Mareckova, 2022. "Modified Causal Forest," Papers 2209.03744, arXiv.org.
    8. Michael C. Knaus & Michael Lechner & Anthony Strittmatter, 2022. "Heterogeneous Employment Effects of Job Search Programs: A Machine Learning Approach," Journal of Human Resources, University of Wisconsin Press, vol. 57(2), pages 597-636.
    9. Michael C Knaus & Michael Lechner & Anthony Strittmatter, 2021. "Machine learning estimation of heterogeneous causal effects: Empirical Monte Carlo evidence," The Econometrics Journal, Royal Economic Society, vol. 24(1), pages 134-161.
    10. Shonosuke Sugasawa & Hisashi Noma, 2021. "Efficient screening of predictive biomarkers for individual treatment selection," Biometrics, The International Biometric Society, vol. 77(1), pages 249-257, March.
    11. Muxuan Liang & Menggang Yu, 2023. "Relative contrast estimation and inference for treatment recommendation," Biometrics, The International Biometric Society, vol. 79(4), pages 2920-2932, December.
    12. Alexander J. Ohnmacht & Arndt Stahler & Sebastian Stintzing & Dominik P. Modest & Julian W. Holch & C. Benedikt Westphalen & Linus Hölzel & Marisa K. Schübel & Ana Galhoz & Ali Farnoud & Minhaz Ud-Dea, 2023. "The Oncology Biomarker Discovery framework reveals cetuximab and bevacizumab response patterns in metastatic colorectal cancer," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    13. Baqun Zhang & Min Zhang, 2018. "C‐learning: A new classification framework to estimate optimal dynamic treatment regimes," Biometrics, The International Biometric Society, vol. 74(3), pages 891-899, September.
    14. Yanqing Wang & Ying‐Qi Zhao & Yingye Zheng, 2020. "Learning‐based biomarker‐assisted rules for optimized clinical benefit under a risk constraint," Biometrics, The International Biometric Society, vol. 76(3), pages 853-862, September.

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