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A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals

Diagnostic histopathology is a gold standard for diagnosing hematopoietic malignancies. Pathologic diagnosis requires labor-intensive reading of a large number of tissue slides with high diagnostic accuracy equal or close to 100 percent to guide treatment options, but this requirement is difficult t...

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Autores principales: Li, Dongguang, Bledsoe, Jacob R., Zeng, Yu, Liu, Wei, Hu, Yiguo, Bi, Ke, Liang, Aibin, Li, Shaoguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691991/
https://www.ncbi.nlm.nih.gov/pubmed/33244018
http://dx.doi.org/10.1038/s41467-020-19817-3
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author Li, Dongguang
Bledsoe, Jacob R.
Zeng, Yu
Liu, Wei
Hu, Yiguo
Bi, Ke
Liang, Aibin
Li, Shaoguang
author_facet Li, Dongguang
Bledsoe, Jacob R.
Zeng, Yu
Liu, Wei
Hu, Yiguo
Bi, Ke
Liang, Aibin
Li, Shaoguang
author_sort Li, Dongguang
collection PubMed
description Diagnostic histopathology is a gold standard for diagnosing hematopoietic malignancies. Pathologic diagnosis requires labor-intensive reading of a large number of tissue slides with high diagnostic accuracy equal or close to 100 percent to guide treatment options, but this requirement is difficult to meet. Although artificial intelligence (AI) helps to reduce the labor of reading pathologic slides, diagnostic accuracy has not reached a clinically usable level. Establishment of an AI model often demands big datasets and an ability to handle large variations in sample preparation and image collection. Here, we establish a highly accurate deep learning platform, consisting of multiple convolutional neural networks, to classify pathologic images by using smaller datasets. We analyze human diffuse large B-cell lymphoma (DLBCL) and non-DLBCL pathologic images from three hospitals separately using AI models, and obtain a diagnostic rate of close to 100 percent (100% for hospital A, 99.71% for hospital B and 100% for hospital C). The technical variability introduced by slide preparation and image collection reduces AI model performance in cross-hospital tests, but the 100% diagnostic accuracy is maintained after its elimination. It is now clinically practical to utilize deep learning models for diagnosis of DLBCL and ultimately other human hematopoietic malignancies.
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spelling pubmed-76919912020-12-03 A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals Li, Dongguang Bledsoe, Jacob R. Zeng, Yu Liu, Wei Hu, Yiguo Bi, Ke Liang, Aibin Li, Shaoguang Nat Commun Article Diagnostic histopathology is a gold standard for diagnosing hematopoietic malignancies. Pathologic diagnosis requires labor-intensive reading of a large number of tissue slides with high diagnostic accuracy equal or close to 100 percent to guide treatment options, but this requirement is difficult to meet. Although artificial intelligence (AI) helps to reduce the labor of reading pathologic slides, diagnostic accuracy has not reached a clinically usable level. Establishment of an AI model often demands big datasets and an ability to handle large variations in sample preparation and image collection. Here, we establish a highly accurate deep learning platform, consisting of multiple convolutional neural networks, to classify pathologic images by using smaller datasets. We analyze human diffuse large B-cell lymphoma (DLBCL) and non-DLBCL pathologic images from three hospitals separately using AI models, and obtain a diagnostic rate of close to 100 percent (100% for hospital A, 99.71% for hospital B and 100% for hospital C). The technical variability introduced by slide preparation and image collection reduces AI model performance in cross-hospital tests, but the 100% diagnostic accuracy is maintained after its elimination. It is now clinically practical to utilize deep learning models for diagnosis of DLBCL and ultimately other human hematopoietic malignancies. Nature Publishing Group UK 2020-11-26 /pmc/articles/PMC7691991/ /pubmed/33244018 http://dx.doi.org/10.1038/s41467-020-19817-3 Text en © The Author(s) 2020 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
Li, Dongguang
Bledsoe, Jacob R.
Zeng, Yu
Liu, Wei
Hu, Yiguo
Bi, Ke
Liang, Aibin
Li, Shaoguang
A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title_full A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title_fullStr A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title_full_unstemmed A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title_short A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals
title_sort deep learning diagnostic platform for diffuse large b-cell lymphoma with high accuracy across multiple hospitals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691991/
https://www.ncbi.nlm.nih.gov/pubmed/33244018
http://dx.doi.org/10.1038/s41467-020-19817-3
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