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Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens

In this pilot study, we introduce a machine learning framework to identify relationships between cancer tissue morphology and hormone receptor pathway activation in breast cancer pathology hematoxylin and eosin (H&E)-stained samples. As a proof-of-concept, we focus on predicting clinical estroge...

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Autores principales: Rawat, Rishi R., Ruderman, Daniel, Macklin, Paul, Rimm, David L., Agus, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123433/
https://www.ncbi.nlm.nih.gov/pubmed/30211313
http://dx.doi.org/10.1038/s41523-018-0084-4
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author Rawat, Rishi R.
Ruderman, Daniel
Macklin, Paul
Rimm, David L.
Agus, David B.
author_facet Rawat, Rishi R.
Ruderman, Daniel
Macklin, Paul
Rimm, David L.
Agus, David B.
author_sort Rawat, Rishi R.
collection PubMed
description In this pilot study, we introduce a machine learning framework to identify relationships between cancer tissue morphology and hormone receptor pathway activation in breast cancer pathology hematoxylin and eosin (H&E)-stained samples. As a proof-of-concept, we focus on predicting clinical estrogen receptor (ER) status—defined as greater than one percent of cells positive for estrogen receptor by immunohistochemistry staining—from spatial arrangement of nuclear features. Our learning pipeline segments nuclei from H&E images, extracts their position, shape and orientation descriptors, and then passes them to a deep neural network to predict ER status. After training on 57 tissue cores of invasive ductal carcinoma (IDC), our pipeline predicted ER status in an independent test set of patient samples (AUC ROC = 0.72, 95%CI = 0.55–0.89, n = 56). This proof of concept shows that machine-derived descriptors of morphologic histology patterns can be correlated to signaling pathway status. Unlike other deep learning approaches to pathology, our system uses deep neural networks to learn spatial relationships between pre-defined biological features, which improves the interpretability of the system and sheds light on the features the neural network uses to predict ER status. Future studies will correlate morphometry to quantitative measures of estrogen receptor status and, ultimately response to hormonal therapy.
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spelling pubmed-61234332018-09-12 Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens Rawat, Rishi R. Ruderman, Daniel Macklin, Paul Rimm, David L. Agus, David B. NPJ Breast Cancer Article In this pilot study, we introduce a machine learning framework to identify relationships between cancer tissue morphology and hormone receptor pathway activation in breast cancer pathology hematoxylin and eosin (H&E)-stained samples. As a proof-of-concept, we focus on predicting clinical estrogen receptor (ER) status—defined as greater than one percent of cells positive for estrogen receptor by immunohistochemistry staining—from spatial arrangement of nuclear features. Our learning pipeline segments nuclei from H&E images, extracts their position, shape and orientation descriptors, and then passes them to a deep neural network to predict ER status. After training on 57 tissue cores of invasive ductal carcinoma (IDC), our pipeline predicted ER status in an independent test set of patient samples (AUC ROC = 0.72, 95%CI = 0.55–0.89, n = 56). This proof of concept shows that machine-derived descriptors of morphologic histology patterns can be correlated to signaling pathway status. Unlike other deep learning approaches to pathology, our system uses deep neural networks to learn spatial relationships between pre-defined biological features, which improves the interpretability of the system and sheds light on the features the neural network uses to predict ER status. Future studies will correlate morphometry to quantitative measures of estrogen receptor status and, ultimately response to hormonal therapy. Nature Publishing Group UK 2018-09-04 /pmc/articles/PMC6123433/ /pubmed/30211313 http://dx.doi.org/10.1038/s41523-018-0084-4 Text en © The Author(s) 2018 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/.
spellingShingle Article
Rawat, Rishi R.
Ruderman, Daniel
Macklin, Paul
Rimm, David L.
Agus, David B.
Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title_full Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title_fullStr Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title_full_unstemmed Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title_short Correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
title_sort correlating nuclear morphometric patterns with estrogen receptor status in breast cancer pathologic specimens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123433/
https://www.ncbi.nlm.nih.gov/pubmed/30211313
http://dx.doi.org/10.1038/s41523-018-0084-4
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