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Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer

The biological complexity reflected in histology images requires advanced approaches for unbiased prognostication. Machine learning and particularly deep learning methods are increasingly applied in the field of digital pathology. In this study, we propose new ways to predict risk for cancer‐specifi...

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Autores principales: Meier, Armin, Nekolla, Katharina, Hewitt, Lindsay C, Earle, Sophie, Yoshikawa, Takaki, Oshima, Takashi, Miyagi, Yohei, Huss, Ralf, Schmidt, Günter, Grabsch, Heike I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578283/
https://www.ncbi.nlm.nih.gov/pubmed/32592447
http://dx.doi.org/10.1002/cjp2.170
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author Meier, Armin
Nekolla, Katharina
Hewitt, Lindsay C
Earle, Sophie
Yoshikawa, Takaki
Oshima, Takashi
Miyagi, Yohei
Huss, Ralf
Schmidt, Günter
Grabsch, Heike I
author_facet Meier, Armin
Nekolla, Katharina
Hewitt, Lindsay C
Earle, Sophie
Yoshikawa, Takaki
Oshima, Takashi
Miyagi, Yohei
Huss, Ralf
Schmidt, Günter
Grabsch, Heike I
author_sort Meier, Armin
collection PubMed
description The biological complexity reflected in histology images requires advanced approaches for unbiased prognostication. Machine learning and particularly deep learning methods are increasingly applied in the field of digital pathology. In this study, we propose new ways to predict risk for cancer‐specific death from digital images of immunohistochemically (IHC) stained tissue microarrays (TMAs). Specifically, we evaluated a cohort of 248 gastric cancer patients using convolutional neural networks (CNNs) in an end‐to‐end weakly supervised scheme independent of subjective pathologist input. To account for the time‐to‐event characteristic of the outcome data, we developed new survival models to guide the network training. In addition to the standard H&E staining, we investigated the prognostic value of a panel of immune cell markers (CD8, CD20, CD68) and a proliferation marker (Ki67). Our CNN‐derived risk scores provided additional prognostic value when compared to the gold standard prognostic tool TNM stage. The CNN‐derived risk scores were also shown to be superior when systematically compared to cell density measurements or a CNN score derived from binary 5‐year survival classification, which ignores time‐to‐event. To better understand the underlying biological mechanisms, we qualitatively investigated risk heat maps for each marker which visualised the network output. We identified patterns of biological interest that were related to low risk of cancer‐specific death such as the presence of B‐cell predominated clusters and Ki67 positive sub‐regions and showed that the corresponding risk scores had prognostic value in multivariate Cox regression analyses (Ki67&CD20 risks: hazard ratio (HR) = 1.47, 95% confidence interval (CI) = 1.15–1.89, p = 0.002; CD20&CD68 risks: HR = 1.33, 95% CI = 1.07–1.67, p = 0.009). Our study demonstrates the potential additional value that deep learning in combination with a panel of IHC markers can bring to the field of precision oncology.
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spelling pubmed-75782832020-10-23 Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer Meier, Armin Nekolla, Katharina Hewitt, Lindsay C Earle, Sophie Yoshikawa, Takaki Oshima, Takashi Miyagi, Yohei Huss, Ralf Schmidt, Günter Grabsch, Heike I J Pathol Clin Res Original Articles The biological complexity reflected in histology images requires advanced approaches for unbiased prognostication. Machine learning and particularly deep learning methods are increasingly applied in the field of digital pathology. In this study, we propose new ways to predict risk for cancer‐specific death from digital images of immunohistochemically (IHC) stained tissue microarrays (TMAs). Specifically, we evaluated a cohort of 248 gastric cancer patients using convolutional neural networks (CNNs) in an end‐to‐end weakly supervised scheme independent of subjective pathologist input. To account for the time‐to‐event characteristic of the outcome data, we developed new survival models to guide the network training. In addition to the standard H&E staining, we investigated the prognostic value of a panel of immune cell markers (CD8, CD20, CD68) and a proliferation marker (Ki67). Our CNN‐derived risk scores provided additional prognostic value when compared to the gold standard prognostic tool TNM stage. The CNN‐derived risk scores were also shown to be superior when systematically compared to cell density measurements or a CNN score derived from binary 5‐year survival classification, which ignores time‐to‐event. To better understand the underlying biological mechanisms, we qualitatively investigated risk heat maps for each marker which visualised the network output. We identified patterns of biological interest that were related to low risk of cancer‐specific death such as the presence of B‐cell predominated clusters and Ki67 positive sub‐regions and showed that the corresponding risk scores had prognostic value in multivariate Cox regression analyses (Ki67&CD20 risks: hazard ratio (HR) = 1.47, 95% confidence interval (CI) = 1.15–1.89, p = 0.002; CD20&CD68 risks: HR = 1.33, 95% CI = 1.07–1.67, p = 0.009). Our study demonstrates the potential additional value that deep learning in combination with a panel of IHC markers can bring to the field of precision oncology. John Wiley & Sons, Inc. 2020-06-27 /pmc/articles/PMC7578283/ /pubmed/32592447 http://dx.doi.org/10.1002/cjp2.170 Text en © 2020 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Meier, Armin
Nekolla, Katharina
Hewitt, Lindsay C
Earle, Sophie
Yoshikawa, Takaki
Oshima, Takashi
Miyagi, Yohei
Huss, Ralf
Schmidt, Günter
Grabsch, Heike I
Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title_full Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title_fullStr Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title_full_unstemmed Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title_short Hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
title_sort hypothesis‐free deep survival learning applied to the tumour microenvironment in gastric cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578283/
https://www.ncbi.nlm.nih.gov/pubmed/32592447
http://dx.doi.org/10.1002/cjp2.170
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