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Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer

BACKGROUND: New biomarkers of risk may improve breast cancer (BC) risk prediction. We developed a computational pathology method to segment benign breast disease (BBD) whole slide images into epithelium, fibrous stroma, and fat. We applied our method to the BBD BC nested case-control study within th...

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Autores principales: Vellal, Adithya D, Sirinukunwattan, Korsuk, Kensler, Kevin H, Baker, Gabrielle M, Stancu, Andreea L, Pyle, Michael E, Collins, Laura C, Schnitt, Stuart J, Connolly, James L, Veta, Mitko, Eliassen, A Heather, Tamimi, Rulla M, Heng, Yujing J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898083/
https://www.ncbi.nlm.nih.gov/pubmed/33644680
http://dx.doi.org/10.1093/jncics/pkaa119
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author Vellal, Adithya D
Sirinukunwattan, Korsuk
Kensler, Kevin H
Baker, Gabrielle M
Stancu, Andreea L
Pyle, Michael E
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Veta, Mitko
Eliassen, A Heather
Tamimi, Rulla M
Heng, Yujing J
author_facet Vellal, Adithya D
Sirinukunwattan, Korsuk
Kensler, Kevin H
Baker, Gabrielle M
Stancu, Andreea L
Pyle, Michael E
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Veta, Mitko
Eliassen, A Heather
Tamimi, Rulla M
Heng, Yujing J
author_sort Vellal, Adithya D
collection PubMed
description BACKGROUND: New biomarkers of risk may improve breast cancer (BC) risk prediction. We developed a computational pathology method to segment benign breast disease (BBD) whole slide images into epithelium, fibrous stroma, and fat. We applied our method to the BBD BC nested case-control study within the Nurses’ Health Studies to assess whether computer-derived tissue composition or a morphometric signature was associated with subsequent risk of BC. METHODS: Tissue segmentation and nuclei detection deep-learning networks were established and applied to 3795 whole slide images from 293 cases who developed BC and 1132 controls who did not. Percentages of each tissue region were calculated, and 615 morphometric features were extracted. Elastic net regression was used to create a BC morphometric signature. Associations between BC risk factors and age-adjusted tissue composition among controls were assessed using analysis of covariance. Unconditional logistic regression, adjusting for the matching factors, BBD histological subtypes, parity, menopausal status, and body mass index evaluated the relationship between tissue composition and BC risk. All statistical tests were 2-sided. RESULTS: Among controls, direction of associations between BBD subtypes, parity, and number of births with breast composition varied by tissue region; select regions were associated with childhood body size, body mass index, age of menarche, and menopausal status (all P < .05). A higher proportion of epithelial tissue was associated with increased BC risk (odds ratio = 1.39, 95% confidence interval = 0.91 to 2.14, for highest vs lowest quartiles, P(trend) = .047). No morphometric signature was associated with BC. CONCLUSIONS: The amount of epithelial tissue may be incorporated into risk assessment models to improve BC risk prediction.
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spelling pubmed-78980832021-02-25 Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer Vellal, Adithya D Sirinukunwattan, Korsuk Kensler, Kevin H Baker, Gabrielle M Stancu, Andreea L Pyle, Michael E Collins, Laura C Schnitt, Stuart J Connolly, James L Veta, Mitko Eliassen, A Heather Tamimi, Rulla M Heng, Yujing J JNCI Cancer Spectr Article BACKGROUND: New biomarkers of risk may improve breast cancer (BC) risk prediction. We developed a computational pathology method to segment benign breast disease (BBD) whole slide images into epithelium, fibrous stroma, and fat. We applied our method to the BBD BC nested case-control study within the Nurses’ Health Studies to assess whether computer-derived tissue composition or a morphometric signature was associated with subsequent risk of BC. METHODS: Tissue segmentation and nuclei detection deep-learning networks were established and applied to 3795 whole slide images from 293 cases who developed BC and 1132 controls who did not. Percentages of each tissue region were calculated, and 615 morphometric features were extracted. Elastic net regression was used to create a BC morphometric signature. Associations between BC risk factors and age-adjusted tissue composition among controls were assessed using analysis of covariance. Unconditional logistic regression, adjusting for the matching factors, BBD histological subtypes, parity, menopausal status, and body mass index evaluated the relationship between tissue composition and BC risk. All statistical tests were 2-sided. RESULTS: Among controls, direction of associations between BBD subtypes, parity, and number of births with breast composition varied by tissue region; select regions were associated with childhood body size, body mass index, age of menarche, and menopausal status (all P < .05). A higher proportion of epithelial tissue was associated with increased BC risk (odds ratio = 1.39, 95% confidence interval = 0.91 to 2.14, for highest vs lowest quartiles, P(trend) = .047). No morphometric signature was associated with BC. CONCLUSIONS: The amount of epithelial tissue may be incorporated into risk assessment models to improve BC risk prediction. Oxford University Press 2021-01-11 /pmc/articles/PMC7898083/ /pubmed/33644680 http://dx.doi.org/10.1093/jncics/pkaa119 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (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 Article
Vellal, Adithya D
Sirinukunwattan, Korsuk
Kensler, Kevin H
Baker, Gabrielle M
Stancu, Andreea L
Pyle, Michael E
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Veta, Mitko
Eliassen, A Heather
Tamimi, Rulla M
Heng, Yujing J
Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title_full Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title_fullStr Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title_full_unstemmed Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title_short Deep Learning Image Analysis of Benign Breast Disease to Identify Subsequent Risk of Breast Cancer
title_sort deep learning image analysis of benign breast disease to identify subsequent risk of breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898083/
https://www.ncbi.nlm.nih.gov/pubmed/33644680
http://dx.doi.org/10.1093/jncics/pkaa119
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