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Hauptverfasser: Fernandes, Alex, Porcher, Raphaël, Tran, Viet-Thi, Petit, François
Format: Preprint
Veröffentlicht: 2025
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Online-Zugang:https://arxiv.org/abs/2507.16048
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author Fernandes, Alex
Porcher, Raphaël
Tran, Viet-Thi
Petit, François
author_facet Fernandes, Alex
Porcher, Raphaël
Tran, Viet-Thi
Petit, François
contents This study investigates the use of virtual patient data to augment control arms in randomised controlled trials (RCTs). Using data from the IST and IST3 trials, we simulated RCTs in which the recruitment in the control arms would stop after a fraction of the initially planned sample size, and would be completed by virtual patients generated by CTGAN and TVAE, two AI algorithms trained on the recruited control patients. In IST, the absolute risk difference(ARD) on death or dependency at 14 days was -0.012 (SE 0.014). Completing the control arm by CTGAN-generated virtual patients after the recruitment of 10% and 50% of participants, yielded an ARD of 0.004 (SE 0.014) (relative difference 133%) and -0.021 (SE 0.014) (relative difference 76%), respectively. Results were comparable with IST3 or TVAE. This is the first empirical demonstration of the risk of errors and misleading conclusions associated with generating virtual controls solely from trial data.
format Preprint
id arxiv_https___arxiv_org_abs_2507_16048
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Evaluating virtual-control-augmented trials for reproducing treatment effect from original RCTs
Fernandes, Alex
Porcher, Raphaël
Tran, Viet-Thi
Petit, François
Methodology
Applications
J.3
This study investigates the use of virtual patient data to augment control arms in randomised controlled trials (RCTs). Using data from the IST and IST3 trials, we simulated RCTs in which the recruitment in the control arms would stop after a fraction of the initially planned sample size, and would be completed by virtual patients generated by CTGAN and TVAE, two AI algorithms trained on the recruited control patients. In IST, the absolute risk difference(ARD) on death or dependency at 14 days was -0.012 (SE 0.014). Completing the control arm by CTGAN-generated virtual patients after the recruitment of 10% and 50% of participants, yielded an ARD of 0.004 (SE 0.014) (relative difference 133%) and -0.021 (SE 0.014) (relative difference 76%), respectively. Results were comparable with IST3 or TVAE. This is the first empirical demonstration of the risk of errors and misleading conclusions associated with generating virtual controls solely from trial data.
title Evaluating virtual-control-augmented trials for reproducing treatment effect from original RCTs
topic Methodology
Applications
J.3
url https://arxiv.org/abs/2507.16048