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Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence
Gene expression-based recurrence assays are strongly recommended to guide the use of chemotherapy in hormone receptor-positive, HER2-negative breast cancer, but such testing is expensive, can contribute to delays in care, and may not be available in low-resource settings. Here, we describe the train...
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/PMC10104799/ https://www.ncbi.nlm.nih.gov/pubmed/37059742 http://dx.doi.org/10.1038/s41523-023-00530-5 |
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author | Howard, Frederick M. Dolezal, James Kochanny, Sara Khramtsova, Galina Vickery, Jasmine Srisuwananukorn, Andrew Woodard, Anna Chen, Nan Nanda, Rita Perou, Charles M. Olopade, Olufunmilayo I. Huo, Dezheng Pearson, Alexander T. |
author_facet | Howard, Frederick M. Dolezal, James Kochanny, Sara Khramtsova, Galina Vickery, Jasmine Srisuwananukorn, Andrew Woodard, Anna Chen, Nan Nanda, Rita Perou, Charles M. Olopade, Olufunmilayo I. Huo, Dezheng Pearson, Alexander T. |
author_sort | Howard, Frederick M. |
collection | PubMed |
description | Gene expression-based recurrence assays are strongly recommended to guide the use of chemotherapy in hormone receptor-positive, HER2-negative breast cancer, but such testing is expensive, can contribute to delays in care, and may not be available in low-resource settings. Here, we describe the training and independent validation of a deep learning model that predicts recurrence assay result and risk of recurrence using both digital histology and clinical risk factors. We demonstrate that this approach outperforms an established clinical nomogram (area under the receiver operating characteristic curve of 0.83 versus 0.76 in an external validation cohort, p = 0.0005) and can identify a subset of patients with excellent prognoses who may not need further genomic testing. |
format | Online Article Text |
id | pubmed-10104799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101047992023-04-16 Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence Howard, Frederick M. Dolezal, James Kochanny, Sara Khramtsova, Galina Vickery, Jasmine Srisuwananukorn, Andrew Woodard, Anna Chen, Nan Nanda, Rita Perou, Charles M. Olopade, Olufunmilayo I. Huo, Dezheng Pearson, Alexander T. NPJ Breast Cancer Brief Communication Gene expression-based recurrence assays are strongly recommended to guide the use of chemotherapy in hormone receptor-positive, HER2-negative breast cancer, but such testing is expensive, can contribute to delays in care, and may not be available in low-resource settings. Here, we describe the training and independent validation of a deep learning model that predicts recurrence assay result and risk of recurrence using both digital histology and clinical risk factors. We demonstrate that this approach outperforms an established clinical nomogram (area under the receiver operating characteristic curve of 0.83 versus 0.76 in an external validation cohort, p = 0.0005) and can identify a subset of patients with excellent prognoses who may not need further genomic testing. Nature Publishing Group UK 2023-04-14 /pmc/articles/PMC10104799/ /pubmed/37059742 http://dx.doi.org/10.1038/s41523-023-00530-5 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Howard, Frederick M. Dolezal, James Kochanny, Sara Khramtsova, Galina Vickery, Jasmine Srisuwananukorn, Andrew Woodard, Anna Chen, Nan Nanda, Rita Perou, Charles M. Olopade, Olufunmilayo I. Huo, Dezheng Pearson, Alexander T. Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title | Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title_full | Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title_fullStr | Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title_full_unstemmed | Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title_short | Integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
title_sort | integration of clinical features and deep learning on pathology for the prediction of breast cancer recurrence assays and risk of recurrence |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104799/ https://www.ncbi.nlm.nih.gov/pubmed/37059742 http://dx.doi.org/10.1038/s41523-023-00530-5 |
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