4.6 Article

An Evolutionary Algorithm to Personalize Stool-Based Colorectal Cancer Screening

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FRONTIERS IN PHYSIOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2021.718276

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colorectal cancer; personalized screening; fecal immunochemical test; screening interval; cutoff; microsimulation models; evolutionary algorithm; FIT-history

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This study presents a broadly applicable algorithm to efficiently optimize personalized screening policies for colorectal cancer (CRC) based on age and FIT-history. The algorithm combines a mathematical framework with an established microsimulation model to accurately estimate the costs and benefits of generated policies. The results demonstrate that personalized screening can increase health benefits compared to traditional screening, and the generated policies have concordant features with current screening recommendations.
BackgroundFecal immunochemical testing (FIT) is an established method for colorectal cancer (CRC) screening. Measured FIT-concentrations are associated with both present and future risk of CRC, and may be used for personalized screening. However, evaluation of personalized screening is computationally challenging. In this study, a broadly applicable algorithm is presented to efficiently optimize personalized screening policies that prescribe screening intervals and FIT-cutoffs, based on age and FIT-history. MethodsWe present a mathematical framework for personalized screening policies and a bi-objective evolutionary algorithm that identifies policies with minimal costs and maximal health benefits. The algorithm is combined with an established microsimulation model (MISCAN-Colon), to accurately estimate the costs and benefits of generated policies, without restrictive Markov assumptions. The performance of the algorithm is demonstrated in three experiments. ResultsIn Experiment 1, a relatively small benchmark problem, the optimal policies were known. The algorithm approached the maximum feasible benefits with a relative difference of 0.007%. Experiment 2 optimized both intervals and cutoffs, Experiment 3 optimized cutoffs only. Optimal policies in both experiments are unknown. Compared to policies recently evaluated for the USPSTF, personalized screening increased health benefits up to 14 and 4.3%, for Experiments 2 and 3, respectively, without adding costs. Generated policies have several features concordant with current screening recommendations. DiscussionThe method presented in this paper is flexible and capable of optimizing personalized screening policies evaluated with computationally-intensive but established simulation models. It can be used to inform screening policies for CRC or other diseases. For CRC, more debate is needed on what features a policy needs to exhibit to make it suitable for implementation in practice.

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