Evidence map›Paper›PMID 41858292›Full record

ArticleAmerican journal of epidemiology2026

Machine learning methods for estimating personalized treatment effects-insights on validity from two large trials.

Hongruyu Chen, Helena Aebersold, Milo Alan Puhan, Miquel Serra-Burriel

Abstract read
In one paragraph

Article in American journal of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hongruyu ChenEpidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland.
Helena AebersoldEpidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland.
Milo Alan PuhanEpidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-4721-1879
Miquel Serra-BurrielEpidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland.

Funding

SBFI (Swiss State Secretariat for Education and Innovation) 24.00027SNSF (Swiss National Science Foundation) 216636
6 · The paper itself

Abstract

Machine learning (ML) methods have the potential to improve precision medicine by estimating personalized treatment effects. However, formal validation of these methods remains limited, leaving their reliability in empirical settings largely uncertain. In this study, we evaluated the internal and external validity of 17 causal heterogeneity ML methods-including metalearners, tree-based methods, and deep learning methods-using data from two large randomized controlled trials: the International Stroke Trial (n = 19 435) and the Chinese Acute Stroke Trial (n = 21 106). We assessed performance using three visual-based metrics and three quantitative metrics. Our analysis found that none of the ML methods consistently demonstrated reliable performance, neither internal nor external. Heterogeneous treatment effects estimated from training data failed to generalize to the test data, even in the absence of distribution shifts. These results raise concerns about the current applicability of ML models in precision medicine and highlight the need for more robust validation techniques to ensure generalizability.

Indexed as

Machine LearningPrecision MedicineStrokeHumansPredictive Learning ModelsRandomized Controlled Trials as TopicReproducibility of ResultsTreatment Effect Heterogeneitycausal machine learningindividualized treatment effectsvalidation

Identifiers

PMID41858292
PMCPMC13437088

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.