Cargando…

Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction

We propose a deep learning workflow for the classification of hematoxylin and eosin stained histological whole-slide images of non-small-cell lung cancer. The workflow includes automatic extraction of meta-features for the characterization of the tumor. We show that the tissue-classification produce...

Descripción completa

Detalles Bibliográficos
Autores principales: Bug, Daniel, Feuerhake, Friedrich, Oswald, Eva, Schüler, Julia, Merhof, Dorit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642041/
https://www.ncbi.nlm.nih.gov/pubmed/31360306
http://dx.doi.org/10.18632/oncotarget.27069
_version_ 1783436901326258176
author Bug, Daniel
Feuerhake, Friedrich
Oswald, Eva
Schüler, Julia
Merhof, Dorit
author_facet Bug, Daniel
Feuerhake, Friedrich
Oswald, Eva
Schüler, Julia
Merhof, Dorit
author_sort Bug, Daniel
collection PubMed
description We propose a deep learning workflow for the classification of hematoxylin and eosin stained histological whole-slide images of non-small-cell lung cancer. The workflow includes automatic extraction of meta-features for the characterization of the tumor. We show that the tissue-classification produces state-of-the-art results with an average F1-score of 83%. Manual supervision indicates that experts, in practice, accept a far higher percentage of predictions. Furthermore, the extracted meta-features are validated via visualization revealing relevant biomedical relations between the different tissue classes. In a hypothetical decision-support scenario, these meta-features can be used to discriminate the tumor response with regard to available treatment options with an estimated accuracy of 84%. This workflow supports large-scale analysis of tissue obtained in preclinical animal experiments, enables reproducible quantification of tissue classes and immune system markers, and paves the way towards discovery of novel features predicting response in translational immune-oncology research.
format Online
Article
Text
id pubmed-6642041
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-66420412019-07-29 Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction Bug, Daniel Feuerhake, Friedrich Oswald, Eva Schüler, Julia Merhof, Dorit Oncotarget Research Paper We propose a deep learning workflow for the classification of hematoxylin and eosin stained histological whole-slide images of non-small-cell lung cancer. The workflow includes automatic extraction of meta-features for the characterization of the tumor. We show that the tissue-classification produces state-of-the-art results with an average F1-score of 83%. Manual supervision indicates that experts, in practice, accept a far higher percentage of predictions. Furthermore, the extracted meta-features are validated via visualization revealing relevant biomedical relations between the different tissue classes. In a hypothetical decision-support scenario, these meta-features can be used to discriminate the tumor response with regard to available treatment options with an estimated accuracy of 84%. This workflow supports large-scale analysis of tissue obtained in preclinical animal experiments, enables reproducible quantification of tissue classes and immune system markers, and paves the way towards discovery of novel features predicting response in translational immune-oncology research. Impact Journals LLC 2019-07-16 /pmc/articles/PMC6642041/ /pubmed/31360306 http://dx.doi.org/10.18632/oncotarget.27069 Text en Copyright: © 2019 Bug et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Bug, Daniel
Feuerhake, Friedrich
Oswald, Eva
Schüler, Julia
Merhof, Dorit
Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title_full Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title_fullStr Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title_full_unstemmed Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title_short Semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
title_sort semi-automated analysis of digital whole slides from humanized lung-cancer xenograft models for checkpoint inhibitor response prediction
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642041/
https://www.ncbi.nlm.nih.gov/pubmed/31360306
http://dx.doi.org/10.18632/oncotarget.27069
work_keys_str_mv AT bugdaniel semiautomatedanalysisofdigitalwholeslidesfromhumanizedlungcancerxenograftmodelsforcheckpointinhibitorresponseprediction
AT feuerhakefriedrich semiautomatedanalysisofdigitalwholeslidesfromhumanizedlungcancerxenograftmodelsforcheckpointinhibitorresponseprediction
AT oswaldeva semiautomatedanalysisofdigitalwholeslidesfromhumanizedlungcancerxenograftmodelsforcheckpointinhibitorresponseprediction
AT schulerjulia semiautomatedanalysisofdigitalwholeslidesfromhumanizedlungcancerxenograftmodelsforcheckpointinhibitorresponseprediction
AT merhofdorit semiautomatedanalysisofdigitalwholeslidesfromhumanizedlungcancerxenograftmodelsforcheckpointinhibitorresponseprediction