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Assessing the Role of Patient Generation Techniques in Virtual Clinical Trial Outcomes

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Abstract

Virtual clinical trials (VCTs) are growing in popularity as a tool for quantitatively predicting heterogeneous treatment responses across a population. In the context of a VCT, a plausible patient is an instance of a mathematical model with parameter (or attribute) values chosen to reflect features of the disease and response to treatment for that particular patient. A number of techniques have been introduced to determine the set of model parametrizations to include in a virtual patient cohort. These methodologies generally start with a prior distribution for each model parameter and utilize some criteria to determine whether a parameter set sampled from the priors should be included or excluded from the plausible population. No standard technique exists, however, for generating these prior distributions and choosing the inclusion/exclusion criteria. In this work, we rigorously quantify the impact that VCT design choices have on VCT predictions. Rather than use real data and a complex mathematical model, a spatial model of radiotherapy is used to generate simulated patient data and the mathematical model used to describe the patient data is a two-parameter ordinary differential equations model. This controlled setup allows us to isolate the impact of both the prior distribution and the inclusion/exclusion criteria on both the heterogeneity of plausible populations and on predicted treatment response. We find that the prior distribution, rather than the inclusion/exclusion criteria, has a larger impact on the heterogeneity of the plausible population. Yet, the percent of treatment responders in the plausible population was more sensitive to the inclusion/exclusion criteria utilized. This foundational understanding of the role of virtual clinical trial design should help inform the development of future VCTs that use more complex models and real data.

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Acknowledgements

The authors thank Katie Storey for her support in implementing the cellular automaton model to generate simulated patient data. JLG acknowledges the use of the ELSA high performance computing cluster at The College of New Jersey for conducting the research reported in this paper. This cluster is funded in part by the National Science Foundation under grant numbers OAC-1826915 and OAC-2320244.

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Correspondence to Jana L. Gevertz.

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The authors have no relevant financial or non-financial interests to disclose. The code used to generate all the data presented in this manuscript is available at https://github.com/jgevertz/VCT.

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Gevertz, J.L., Wares, J.R. Assessing the Role of Patient Generation Techniques in Virtual Clinical Trial Outcomes. Bull Math Biol 86, 119 (2024). https://doi.org/10.1007/s11538-024-01345-6

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  • DOI: https://doi.org/10.1007/s11538-024-01345-6

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