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Conformal prediction for dose-response models with continuous treatments

 
cris.virtual.department#PLACEHOLDER_PARENT_METADATA_VALUE#
cris.virtual.department#PLACEHOLDER_PARENT_METADATA_VALUE#
cris.virtual.orcid0000-0002-3322-150X
cris.virtual.orcid0000-0002-7865-6793
cris.virtualsource.department7e4e6acb-503e-46de-8da7-7be193b6ca37
cris.virtualsource.department43fd6f27-126a-4a10-8c2e-2c15e86e4898
cris.virtualsource.orcid7e4e6acb-503e-46de-8da7-7be193b6ca37
cris.virtualsource.orcid43fd6f27-126a-4a10-8c2e-2c15e86e4898
dc.contributor.authorVerhaeghe, Jarne
dc.contributor.authorJonkers, Jef
dc.contributor.authorVan Hoecke, Sofie
dc.date.accessioned2026-09-07T14:03:41Z
dc.date.available2026-09-07T14:03:41Z
dc.date.createdwos2026
dc.date.issued2026
dc.description.abstractUnderstanding the dose-response relation between a continuous treatment and the outcome for an individual can greatly drive decision-making, particularly in areas like personalized drug dosing and personalized healthcare interventions. Point estimates are often insufficient in these high-risk environments, highlighting the need for uncertainty quantification to support informed decisions. Conformal prediction, a distribution-free and model-agnostic method for uncertainty quantification, has seen limited application in continuous treatments or dose-response models. To address this gap, we propose a novel methodology that frames the causal dose-response problem as a covariate shift, leveraging weighted conformal prediction. By incorporating propensity estimation, conformal predictive systems, and likelihood ratios, we present a practical solution for generating prediction intervals for dose-response models. Additionally, our method approximates local coverage for every treatment value by applying kernel functions as weights in weighted conformal prediction. Finally, we use a new synthetic and semi-synthetic benchmark dataset to demonstrate the significance of covariate shift assumptions in achieving robust prediction intervals for counterfactual dose-response models.
dc.description.wosFundingTextThis research was funded by the FWO Junior Research project HEROI2C which investigates hybrid machine learning for improved infection management in critically ill patients (Ref. G085920N). Jarne Verhaeghe is funded by the Research Foundation Flanders (FWO, Ref. 1S59522N). Jef Jonkers is funded by the Research Foundation Flanders (FWO, Ref. 1S11525N). Part of this research was supported through the Flemish Government (AI Research Program).
dc.identifier.doi10.1016/j.ijar.2026.109751
dc.identifier.issn0888-613X
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/60234
dc.language.isoeng
dc.provenance.editstepusergreet.vanhoof@imec.be
dc.publisherELSEVIER SCIENCE INC
dc.source.beginpage109751
dc.source.journalINTERNATIONAL JOURNAL OF APPROXIMATE REASONING
dc.source.numberofpages30
dc.source.volume197
dc.subject.keywordsINFERENCE
dc.subject.keywordsDESIGN
dc.title

Conformal prediction for dose-response models with continuous treatments

dc.typeJournal article
dspace.entity.typePublication
imec.internal.crawledAt2026-07-14
imec.internal.sourcecrawler
imec.internal.wosCreatedAt2026-07-14
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