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Application of machine learning methods in clinical trials for precision medicine

OBJECTIVE: A key component for precision medicine is a good prediction algorithm for patients’ response to treatments. We aim to implement machine learning (ML) algorithms into the response-adaptive randomization (RAR) design and improve the treatment outcomes. MATERIALS AND METHODS: We incorporated...

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Autores principales: Wang, Yizhuo, Carter, Bing Z, Li, Ziyi, Huang, Xuelin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846336/
https://www.ncbi.nlm.nih.gov/pubmed/35178503
http://dx.doi.org/10.1093/jamiaopen/ooab107
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author Wang, Yizhuo
Carter, Bing Z
Li, Ziyi
Huang, Xuelin
author_facet Wang, Yizhuo
Carter, Bing Z
Li, Ziyi
Huang, Xuelin
author_sort Wang, Yizhuo
collection PubMed
description OBJECTIVE: A key component for precision medicine is a good prediction algorithm for patients’ response to treatments. We aim to implement machine learning (ML) algorithms into the response-adaptive randomization (RAR) design and improve the treatment outcomes. MATERIALS AND METHODS: We incorporated 9 ML algorithms to model the relationship of patient responses and biomarkers in clinical trial design. Such a model predicted the response rate of each treatment for each new patient and provide guidance for treatment assignment. Realizing that no single method may fit all trials well, we also built an ensemble of these 9 methods. We evaluated their performance through quantifying the benefits for trial participants, such as the overall response rate and the percentage of patients who receive their optimal treatments. RESULTS: Simulation studies showed that the adoption of ML methods resulted in more personalized optimal treatment assignments and higher overall response rates among trial participants. Compared with each individual ML method, the ensemble approach achieved the highest response rate and assigned the largest percentage of patients to their optimal treatments. For the real-world study, we successfully showed the potential improvements if the proposed design had been implemented in the study. CONCLUSION: In summary, the ML-based RAR design is a promising approach for assigning more patients to their personalized effective treatments, which makes the clinical trial more ethical and appealing. These features are especially desirable for late-stage cancer patients who have failed all the Food and Drug Administration (FDA)-approved treatment options and only can get new treatments through clinical trials.
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spelling pubmed-88463362022-02-16 Application of machine learning methods in clinical trials for precision medicine Wang, Yizhuo Carter, Bing Z Li, Ziyi Huang, Xuelin JAMIA Open Research and Applications OBJECTIVE: A key component for precision medicine is a good prediction algorithm for patients’ response to treatments. We aim to implement machine learning (ML) algorithms into the response-adaptive randomization (RAR) design and improve the treatment outcomes. MATERIALS AND METHODS: We incorporated 9 ML algorithms to model the relationship of patient responses and biomarkers in clinical trial design. Such a model predicted the response rate of each treatment for each new patient and provide guidance for treatment assignment. Realizing that no single method may fit all trials well, we also built an ensemble of these 9 methods. We evaluated their performance through quantifying the benefits for trial participants, such as the overall response rate and the percentage of patients who receive their optimal treatments. RESULTS: Simulation studies showed that the adoption of ML methods resulted in more personalized optimal treatment assignments and higher overall response rates among trial participants. Compared with each individual ML method, the ensemble approach achieved the highest response rate and assigned the largest percentage of patients to their optimal treatments. For the real-world study, we successfully showed the potential improvements if the proposed design had been implemented in the study. CONCLUSION: In summary, the ML-based RAR design is a promising approach for assigning more patients to their personalized effective treatments, which makes the clinical trial more ethical and appealing. These features are especially desirable for late-stage cancer patients who have failed all the Food and Drug Administration (FDA)-approved treatment options and only can get new treatments through clinical trials. Oxford University Press 2022-02-08 /pmc/articles/PMC8846336/ /pubmed/35178503 http://dx.doi.org/10.1093/jamiaopen/ooab107 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the American Medical Informatics Association. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research and Applications
Wang, Yizhuo
Carter, Bing Z
Li, Ziyi
Huang, Xuelin
Application of machine learning methods in clinical trials for precision medicine
title Application of machine learning methods in clinical trials for precision medicine
title_full Application of machine learning methods in clinical trials for precision medicine
title_fullStr Application of machine learning methods in clinical trials for precision medicine
title_full_unstemmed Application of machine learning methods in clinical trials for precision medicine
title_short Application of machine learning methods in clinical trials for precision medicine
title_sort application of machine learning methods in clinical trials for precision medicine
topic Research and Applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846336/
https://www.ncbi.nlm.nih.gov/pubmed/35178503
http://dx.doi.org/10.1093/jamiaopen/ooab107
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