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Auteurs principaux: Park, Chan, Chen, Guanhua, Yu, Menggang
Format: Preprint
Publié: 2023
Sujets:
Accès en ligne:https://arxiv.org/abs/2302.12479
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author Park, Chan
Chen, Guanhua
Yu, Menggang
author_facet Park, Chan
Chen, Guanhua
Yu, Menggang
contents In fields such as medicine and social sciences, the goal of treatment is often to maintain the outcome of interest within a desirable range rather than to optimize its value. To achieve this, it may be more practical to recommend a treatment dose interval rather than a single fixed level for a study unit. Since individuals may respond differently to the same treatment level, the recommended dose interval should be personalized based on their unique characteristics. Iterative procedures have been proposed to jointly learn the lower and upper bounds of personalized dose intervals, but they lack theoretical justification. To fill this gap, we propose a method to learn personalized two-sided dose intervals based on empirical risk minimization using a novel loss function. The proposed loss function is designed to be well-defined over a tensor product function space, eliminating the need for iterative procedures. In addition, the loss function is doubly-robust to the misspecification of nuisance functions. We establish statistical properties of the estimated dose interval in terms of excess risk by leveraging the reproducing kernel Hilbert space theory. Our simulation study and real-world applications in warfarin dosing and the Job Corps program show that our proposed direct estimation method outperforms competing methods, including indirect regression-based methods.
format Preprint
id arxiv_https___arxiv_org_abs_2302_12479
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle Personalized Two-sided Dose Interval
Park, Chan
Chen, Guanhua
Yu, Menggang
Methodology
In fields such as medicine and social sciences, the goal of treatment is often to maintain the outcome of interest within a desirable range rather than to optimize its value. To achieve this, it may be more practical to recommend a treatment dose interval rather than a single fixed level for a study unit. Since individuals may respond differently to the same treatment level, the recommended dose interval should be personalized based on their unique characteristics. Iterative procedures have been proposed to jointly learn the lower and upper bounds of personalized dose intervals, but they lack theoretical justification. To fill this gap, we propose a method to learn personalized two-sided dose intervals based on empirical risk minimization using a novel loss function. The proposed loss function is designed to be well-defined over a tensor product function space, eliminating the need for iterative procedures. In addition, the loss function is doubly-robust to the misspecification of nuisance functions. We establish statistical properties of the estimated dose interval in terms of excess risk by leveraging the reproducing kernel Hilbert space theory. Our simulation study and real-world applications in warfarin dosing and the Job Corps program show that our proposed direct estimation method outperforms competing methods, including indirect regression-based methods.
title Personalized Two-sided Dose Interval
topic Methodology
url https://arxiv.org/abs/2302.12479