# Modern approaches for evaluating treatment effect heterogeneity from clinical trials and observational data

arXiv: https://arxiv.org/abs/2311.14889 · HTML: https://mlsanity.com/paper/2311.14889/

## Key facts

- Cited by 4 papers in the map (data through 14 Oct 2026).
- First posted on arXiv 25 Nov 2023.

## Built on by (most cited first, 4 of 4)

- [Overview and practical recommendations on using Shapley Values for identifying predictive biomarkers via CATE modeling](https://mlsanity.com/paper/2505.01145/) (2025)
- [Can Broad Biomedical Knowledge be Contextualized into Scenario-Grounded Propositions?](https://mlsanity.com/paper/2605.27082/) (2026)
- [Subgroup Discovery with the Cox Model](https://mlsanity.com/paper/2512.20762/) (2025)
- [Co-Supervised Tree Synthesis for Interpretable Subgroup Identification and Honest Treatment Effect Inference in Randomized Trials](https://mlsanity.com/paper/2610.03927/) (2026)

## Abstract (arXiv)

In this paper we review recent advances in statistical methods for the evaluation of the heterogeneity of treatment effects (HTE), including subgroup identification and estimation of individualized treatment regimens, from randomized clinical trials and observational studies. We identify several types of approaches using the features introduced in Lipkovich, Dmitrienko and D'Agostino (2017) that distinguish the recommended principled methods from basic methods for HTE evaluation that typically rely on rules of thumb and general guidelines (the methods are often referred to as common practices). We discuss the advantages and disadvantages of various principled methods as well as common measures for evaluating their performance. We use simulated data and a case study based on a historical clinical trial to illustrate several new approaches to HTE evaluation.
