An Estimator-Robust Design for Augmenting Randomized Controlled Trial with External Real-World Data

Fuente: arXiv
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Autori principali: Qiu, Sky, Tarp, Jens, Mertens, Andrew, van der Laan, Mark
Natura: Preprint
Pubblicazione: 2025
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author Qiu, Sky
Tarp, Jens
Mertens, Andrew
van der Laan, Mark
author_facet Qiu, Sky
Tarp, Jens
Mertens, Andrew
van der Laan, Mark
contents Augmenting randomized controlled trials (RCTs) with external real-world data (RWD) has the potential to improve the finite sample efficiency of treatment effect estimators. We describe using adaptive targeted maximum likelihood estimation (A-TMLE) for estimating the average treatment effect (ATE) by decomposing the ATE estimand into two components: a pooled-ATE estimand that combines data from both the RCT and external sources, and a bias estimand that captures the conditional effect of RCT enrollment on the outcome. This approach views the RCT data as the reference and corrects for inconsistencies of any kind between the RCT and the external data source. Given the growing abundance of external RWD from modern electronic health records, determining the optimal strategy to select candidate external patients for data integration remains an open yet critical problem. In this work, we begin by analyzing the robustness property of the A-TMLE estimator and then propose a matching-based sampling strategy that improves the robustness of the estimator with respect to the target estimand. Our proposed strategy is outcome-blind and involves matching based on two one-dimensional scores: the trial enrollment score and the propensity score in the external data. We demonstrate in simulations that our sampling strategy improves the coverage and shortens the widths of confidence intervals produced by A-TMLE. We illustrate our method with a case study of augmenting the DEVOTE cardiovascular safety trial by using the Optum Clinformatics claims database.
format Preprint
id arxiv_https___arxiv_org_abs_2501_17835
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle An Estimator-Robust Design for Augmenting Randomized Controlled Trial with External Real-World Data
Qiu, Sky
Tarp, Jens
Mertens, Andrew
van der Laan, Mark
Methodology
Applications
Augmenting randomized controlled trials (RCTs) with external real-world data (RWD) has the potential to improve the finite sample efficiency of treatment effect estimators. We describe using adaptive targeted maximum likelihood estimation (A-TMLE) for estimating the average treatment effect (ATE) by decomposing the ATE estimand into two components: a pooled-ATE estimand that combines data from both the RCT and external sources, and a bias estimand that captures the conditional effect of RCT enrollment on the outcome. This approach views the RCT data as the reference and corrects for inconsistencies of any kind between the RCT and the external data source. Given the growing abundance of external RWD from modern electronic health records, determining the optimal strategy to select candidate external patients for data integration remains an open yet critical problem. In this work, we begin by analyzing the robustness property of the A-TMLE estimator and then propose a matching-based sampling strategy that improves the robustness of the estimator with respect to the target estimand. Our proposed strategy is outcome-blind and involves matching based on two one-dimensional scores: the trial enrollment score and the propensity score in the external data. We demonstrate in simulations that our sampling strategy improves the coverage and shortens the widths of confidence intervals produced by A-TMLE. We illustrate our method with a case study of augmenting the DEVOTE cardiovascular safety trial by using the Optum Clinformatics claims database.
title An Estimator-Robust Design for Augmenting Randomized Controlled Trial with External Real-World Data
topic Methodology
Applications
url https://arxiv.org/abs/2501.17835