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Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study

BACKGROUND: For virtually every patient with colorectal cancer (CRC), hematoxylin–eosin (HE)–stained tissue slides are available. These images contain quantitative information, which is not routinely used to objectively extract prognostic biomarkers. In the present study, we investigated whether dee...

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Autores principales: Kather, Jakob Nikolas, Krisam, Johannes, Charoentong, Pornpimol, Luedde, Tom, Herpel, Esther, Weis, Cleo-Aron, Gaiser, Timo, Marx, Alexander, Valous, Nektarios A., Ferber, Dyke, Jansen, Lina, Reyes-Aldasoro, Constantino Carlos, Zörnig, Inka, Jäger, Dirk, Brenner, Hermann, Chang-Claude, Jenny, Hoffmeister, Michael, Halama, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345440/
https://www.ncbi.nlm.nih.gov/pubmed/30677016
http://dx.doi.org/10.1371/journal.pmed.1002730
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author Kather, Jakob Nikolas
Krisam, Johannes
Charoentong, Pornpimol
Luedde, Tom
Herpel, Esther
Weis, Cleo-Aron
Gaiser, Timo
Marx, Alexander
Valous, Nektarios A.
Ferber, Dyke
Jansen, Lina
Reyes-Aldasoro, Constantino Carlos
Zörnig, Inka
Jäger, Dirk
Brenner, Hermann
Chang-Claude, Jenny
Hoffmeister, Michael
Halama, Niels
author_facet Kather, Jakob Nikolas
Krisam, Johannes
Charoentong, Pornpimol
Luedde, Tom
Herpel, Esther
Weis, Cleo-Aron
Gaiser, Timo
Marx, Alexander
Valous, Nektarios A.
Ferber, Dyke
Jansen, Lina
Reyes-Aldasoro, Constantino Carlos
Zörnig, Inka
Jäger, Dirk
Brenner, Hermann
Chang-Claude, Jenny
Hoffmeister, Michael
Halama, Niels
author_sort Kather, Jakob Nikolas
collection PubMed
description BACKGROUND: For virtually every patient with colorectal cancer (CRC), hematoxylin–eosin (HE)–stained tissue slides are available. These images contain quantitative information, which is not routinely used to objectively extract prognostic biomarkers. In the present study, we investigated whether deep convolutional neural networks (CNNs) can extract prognosticators directly from these widely available images. METHODS AND FINDINGS: We hand-delineated single-tissue regions in 86 CRC tissue slides, yielding more than 100,000 HE image patches, and used these to train a CNN by transfer learning, reaching a nine-class accuracy of >94% in an independent data set of 7,180 images from 25 CRC patients. With this tool, we performed automated tissue decomposition of representative multitissue HE images from 862 HE slides in 500 stage I–IV CRC patients in the The Cancer Genome Atlas (TCGA) cohort, a large international multicenter collection of CRC tissue. Based on the output neuron activations in the CNN, we calculated a “deep stroma score,” which was an independent prognostic factor for overall survival (OS) in a multivariable Cox proportional hazard model (hazard ratio [HR] with 95% confidence interval [CI]: 1.99 [1.27–3.12], p = 0.0028), while in the same cohort, manual quantification of stromal areas and a gene expression signature of cancer-associated fibroblasts (CAFs) were only prognostic in specific tumor stages. We validated these findings in an independent cohort of 409 stage I–IV CRC patients from the “Darmkrebs: Chancen der Verhütung durch Screening” (DACHS) study who were recruited between 2003 and 2007 in multiple institutions in Germany. Again, the score was an independent prognostic factor for OS (HR 1.63 [1.14–2.33], p = 0.008), CRC-specific OS (HR 2.29 [1.5–3.48], p = 0.0004), and relapse-free survival (RFS; HR 1.92 [1.34–2.76], p = 0.0004). A prospective validation is required before this biomarker can be implemented in clinical workflows. CONCLUSIONS: In our retrospective study, we show that a CNN can assess the human tumor microenvironment and predict prognosis directly from histopathological images.
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spelling pubmed-63454402019-02-02 Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study Kather, Jakob Nikolas Krisam, Johannes Charoentong, Pornpimol Luedde, Tom Herpel, Esther Weis, Cleo-Aron Gaiser, Timo Marx, Alexander Valous, Nektarios A. Ferber, Dyke Jansen, Lina Reyes-Aldasoro, Constantino Carlos Zörnig, Inka Jäger, Dirk Brenner, Hermann Chang-Claude, Jenny Hoffmeister, Michael Halama, Niels PLoS Med Research Article BACKGROUND: For virtually every patient with colorectal cancer (CRC), hematoxylin–eosin (HE)–stained tissue slides are available. These images contain quantitative information, which is not routinely used to objectively extract prognostic biomarkers. In the present study, we investigated whether deep convolutional neural networks (CNNs) can extract prognosticators directly from these widely available images. METHODS AND FINDINGS: We hand-delineated single-tissue regions in 86 CRC tissue slides, yielding more than 100,000 HE image patches, and used these to train a CNN by transfer learning, reaching a nine-class accuracy of >94% in an independent data set of 7,180 images from 25 CRC patients. With this tool, we performed automated tissue decomposition of representative multitissue HE images from 862 HE slides in 500 stage I–IV CRC patients in the The Cancer Genome Atlas (TCGA) cohort, a large international multicenter collection of CRC tissue. Based on the output neuron activations in the CNN, we calculated a “deep stroma score,” which was an independent prognostic factor for overall survival (OS) in a multivariable Cox proportional hazard model (hazard ratio [HR] with 95% confidence interval [CI]: 1.99 [1.27–3.12], p = 0.0028), while in the same cohort, manual quantification of stromal areas and a gene expression signature of cancer-associated fibroblasts (CAFs) were only prognostic in specific tumor stages. We validated these findings in an independent cohort of 409 stage I–IV CRC patients from the “Darmkrebs: Chancen der Verhütung durch Screening” (DACHS) study who were recruited between 2003 and 2007 in multiple institutions in Germany. Again, the score was an independent prognostic factor for OS (HR 1.63 [1.14–2.33], p = 0.008), CRC-specific OS (HR 2.29 [1.5–3.48], p = 0.0004), and relapse-free survival (RFS; HR 1.92 [1.34–2.76], p = 0.0004). A prospective validation is required before this biomarker can be implemented in clinical workflows. CONCLUSIONS: In our retrospective study, we show that a CNN can assess the human tumor microenvironment and predict prognosis directly from histopathological images. Public Library of Science 2019-01-24 /pmc/articles/PMC6345440/ /pubmed/30677016 http://dx.doi.org/10.1371/journal.pmed.1002730 Text en © 2019 Kather et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kather, Jakob Nikolas
Krisam, Johannes
Charoentong, Pornpimol
Luedde, Tom
Herpel, Esther
Weis, Cleo-Aron
Gaiser, Timo
Marx, Alexander
Valous, Nektarios A.
Ferber, Dyke
Jansen, Lina
Reyes-Aldasoro, Constantino Carlos
Zörnig, Inka
Jäger, Dirk
Brenner, Hermann
Chang-Claude, Jenny
Hoffmeister, Michael
Halama, Niels
Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title_full Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title_fullStr Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title_full_unstemmed Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title_short Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study
title_sort predicting survival from colorectal cancer histology slides using deep learning: a retrospective multicenter study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345440/
https://www.ncbi.nlm.nih.gov/pubmed/30677016
http://dx.doi.org/10.1371/journal.pmed.1002730
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