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Improving clinical trial design using interpretable machine learning based prediction of early trial termination
This study proposes using a machine learning pipeline to optimise clinical trial design. The goal is to predict early termination probability of clinical trials using machine learning modelling, and to understand feature contributions driving early termination. This will inform further suggestions t...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813129/ https://www.ncbi.nlm.nih.gov/pubmed/36599880 http://dx.doi.org/10.1038/s41598-023-27416-7 |
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author | Kavalci, Ece Hartshorn, Anthony |
author_facet | Kavalci, Ece Hartshorn, Anthony |
author_sort | Kavalci, Ece |
collection | PubMed |
description | This study proposes using a machine learning pipeline to optimise clinical trial design. The goal is to predict early termination probability of clinical trials using machine learning modelling, and to understand feature contributions driving early termination. This will inform further suggestions to the study protocol to reduce the risk of wasted resources. A dataset containing 420,268 clinical trial records and 24 fields was extracted from the ct.gov registry. In addition to study characteristics features, 12,864 eligibility criteria search features are used, generated using a public annotated eligibility criteria dataset, CHIA. Furthermore, disease categorization features are used allowing a study to belong more than one category specified by clinicaltrials.gov. Ensemble models including random forest and extreme gradient boosting classifiers were used to train and evaluate predictive performance. We achieved a Receiver Operator Characteristic Area under the Curve score of 0.80, and balanced accuracy of 0.70 on the test set using gradient boosting classification. We used Shapley Additive Explanations to interpret the termination predictions to flag feature contributions. The proposed pipeline will lead to an optimised clinical trial design and consequently help potentially life-saving treatments reach patients faster. |
format | Online Article Text |
id | pubmed-9813129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98131292023-01-06 Improving clinical trial design using interpretable machine learning based prediction of early trial termination Kavalci, Ece Hartshorn, Anthony Sci Rep Article This study proposes using a machine learning pipeline to optimise clinical trial design. The goal is to predict early termination probability of clinical trials using machine learning modelling, and to understand feature contributions driving early termination. This will inform further suggestions to the study protocol to reduce the risk of wasted resources. A dataset containing 420,268 clinical trial records and 24 fields was extracted from the ct.gov registry. In addition to study characteristics features, 12,864 eligibility criteria search features are used, generated using a public annotated eligibility criteria dataset, CHIA. Furthermore, disease categorization features are used allowing a study to belong more than one category specified by clinicaltrials.gov. Ensemble models including random forest and extreme gradient boosting classifiers were used to train and evaluate predictive performance. We achieved a Receiver Operator Characteristic Area under the Curve score of 0.80, and balanced accuracy of 0.70 on the test set using gradient boosting classification. We used Shapley Additive Explanations to interpret the termination predictions to flag feature contributions. The proposed pipeline will lead to an optimised clinical trial design and consequently help potentially life-saving treatments reach patients faster. Nature Publishing Group UK 2023-01-04 /pmc/articles/PMC9813129/ /pubmed/36599880 http://dx.doi.org/10.1038/s41598-023-27416-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kavalci, Ece Hartshorn, Anthony Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title | Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title_full | Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title_fullStr | Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title_full_unstemmed | Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title_short | Improving clinical trial design using interpretable machine learning based prediction of early trial termination |
title_sort | improving clinical trial design using interpretable machine learning based prediction of early trial termination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813129/ https://www.ncbi.nlm.nih.gov/pubmed/36599880 http://dx.doi.org/10.1038/s41598-023-27416-7 |
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