Distilling heterogeneous treatment effects: Stable subgroup estimation in causal inference
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Abstract (arXiv)
Recent methodological developments have introduced new black-box approaches to better estimate heterogeneous treatment effects; however, these methods fall short of providing interpretable characterizations of the underlying individuals who may be most at risk or benefit most from receiving the treatment, thereby limiting their practical utility. In this work, we introduce causal distillation trees (CDT) to estimate interpretable subgroups. CDT allows researchers to fit any machine learning model to estimate heterogeneous treatment effects, and then leverages a simple, second-stage tree-based model to "distill" the estimated treatment effects into meaningful subgroups. As a result, CDT inherits the improvements in predictive performance from black-box machine learning models while preserving the interpretability of a simple decision tree. We derive theoretical guarantees for the consistency of the estimated subgroups using CDT, and introduce stability-driven diagnostics for researchers to evaluate the quality of the estimated subgroups. We illustrate our proposed method on a randomized controlled trial of antiretroviral treatment for HIV from the AIDS Clinical Trials Group Study 175 and show that CDT out-performs state-of-the-art approaches in constructing stable, clinically relevant subgroups.
Key facts. Cited by 3 papers in the map (data through 14 Oct 2026). First posted on arXiv 11 Feb 2025.
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Citing papers per year: 2025: 2; 2026: 1.
3 papers.
- 2025Overview and practical recommendations on using Shapley Values for identifying predictive biomarkers via CATE modelingcited by 1
- 2025Learning Subgroups with Maximum Treatment Effects without Causal Heuristicscited by 1
- 2026Co-Supervised Tree Synthesis for Interpretable Subgroup Identification and Honest Treatment Effect Inference in Randomized Trialscited by 0
- 2026Co-Supervised Tree Synthesis for Interpretable Subgroup Identification and Honest Treatment Effect Inference in Randomized Trials2 Oct 2026
- 2025Learning Subgroups with Maximum Treatment Effects without Causal Heuristics25 Nov 2025
- 2025Overview and practical recommendations on using Shapley Values for identifying predictive biomarkers via CATE modeling2 May 2025