Evidence map›Paper›PMID 41035066›Full record

ArticleDiagnostic and prognostic research2025

Counterfactual prediction from machine learning models: transportability and joint analysis for model development and evaluation using multi-source data.

Sarah C Voter, Issa J Dahabreh, Christopher B Boyer, Habib Rahbar, Despina Kontos, Jon A Steingrimsson

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Article in Diagnostic and prognostic research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sarah C VoterDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, USA. sarah_voter@brown.edu.
Issa J DahabrehCAUSALab, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Christopher B BoyerDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Habib RahbarDepartment of Radiology, University of Washington, Seattle, WA, USA.
Despina KontosDepartment of Radiology, University of Pennsylvania, Philadelphia, PA, USA.
Jon A SteingrimssonDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, USA.

Funding

MRI Radiomic Signatures of DCIS to Optimize TreatmentR01CA268341 · NCI · UNIVERSITY OF WASHINGTON · PI Despina Kontos, HABIBOLLAH RAHBAR · 2022 to 2026
$2.8M
NCI NIH HHS R01 CA268341NCI NIH HHS R01 CA268341-01A1
6 · The paper itself

Abstract

backgroundWhen a machine learning model is developed and evaluated in a setting where the treatment assignment process differs from the setting of intended model deployment, failure to account for this difference can lead to suboptimal model development and biased estimates of model performance.

methodsWe consider the setting where data from a randomized trial and an observational study emulating the trial are available for machine learning model development and evaluation. We provide two approaches for estimating the model and assessing model performance under a hypothetical treatment strategy in the target population underlying the observational study. The first approach uses counterfactual predictions from the observational study only and relies on the assumption of conditional exchangeability between treated and untreated individuals (no unmeasured confounding). The second approach leverages the exchangeability between treatment groups in the trial (supported by study design) to "transport" estimates from the trial to the population underlying the observational study, relying on an additional assumption of conditional exchangeability between the populations underlying the observational study and the randomized trial.

resultsWe examine the assumptions underlying both approaches for fitting the model and estimating performance in the target population and provide estimators for both objectives. We then develop a joint estimation strategy that combines data from the trial and the observational study, and discuss benchmarking of the trial and observational results.

conclusionsBoth the observational and transportability analyses can be used to fit a model and estimate performance under a counterfactual treatment strategy in the population underlying the observational data, but they rely on different assumptions. In either case, the assumptions are untestable, and deciding which method is more appropriate requires careful contextual consideration. If all assumptions hold, then combining the data from the observational study and the randomized trial can be used for more efficient estimation.

Indexed as

Counterfactual predictionMachine learningModel evaluationObservational analysisTransportability

Identifiers

PMID41035066
PMCPMC12490139

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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.