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A deep learning framework for automated classification of histopathological kidney whole-slide images

BACKGROUND: Renal cell carcinoma is the most common type of malignant kidney tumor and is responsible for 14,830 deaths per year in the United States. Among the four most common subtypes of renal cell carcinoma, clear cell renal cell carcinoma has the worst prognosis and clear cell papillary renal c...

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Autores principales: Abdeltawab, Hisham A., Khalifa, Fahmi A., Ghazal, Mohammed A., Cheng, Liang, El-Baz, Ayman S., Gondim, Dibson D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576982/
https://www.ncbi.nlm.nih.gov/pubmed/36268061
http://dx.doi.org/10.1016/j.jpi.2022.100093
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author Abdeltawab, Hisham A.
Khalifa, Fahmi A.
Ghazal, Mohammed A.
Cheng, Liang
El-Baz, Ayman S.
Gondim, Dibson D.
author_facet Abdeltawab, Hisham A.
Khalifa, Fahmi A.
Ghazal, Mohammed A.
Cheng, Liang
El-Baz, Ayman S.
Gondim, Dibson D.
author_sort Abdeltawab, Hisham A.
collection PubMed
description BACKGROUND: Renal cell carcinoma is the most common type of malignant kidney tumor and is responsible for 14,830 deaths per year in the United States. Among the four most common subtypes of renal cell carcinoma, clear cell renal cell carcinoma has the worst prognosis and clear cell papillary renal cell carcinoma appears to have no malignant potential. Distinction between these two subtypes can be difficult due to morphologic overlap on examination of histopathological preparation stained with hematoxylin and eosin. Ancillary techniques, such as immunohistochemistry, can be helpful, but they are not universally available. We propose and evaluate a new deep learning framework for tumor classification tasks to distinguish clear cell renal cell carcinoma from papillary renal cell carcinoma. METHODS: Our deep learning framework is composed of three convolutional neural networks. We divided whole-slide kidney images into patches with three different sizes where each network processes a specific patch size. Our framework provides patchwise and pixelwise classification. The histopathological kidney data is composed of 64 image slides that belong to 4 categories: fat, parenchyma, clear cell renal cell carcinoma, and clear cell papillary renal cell carcinoma. The final output of our framework is an image map where each pixel is classified into one class. To maintain consistency, we processed the map with Gauss-Markov random field smoothing. RESULTS: Our framework succeeded in classifying the four classes and showed superior performance compared to well-established state-of-the-art methods (pixel accuracy: 0.89 ResNet18, 0.92 proposed). CONCLUSIONS: Deep learning techniques have a significant potential for cancer diagnosis.
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spelling pubmed-95769822022-10-19 A deep learning framework for automated classification of histopathological kidney whole-slide images Abdeltawab, Hisham A. Khalifa, Fahmi A. Ghazal, Mohammed A. Cheng, Liang El-Baz, Ayman S. Gondim, Dibson D. J Pathol Inform Original Research Article BACKGROUND: Renal cell carcinoma is the most common type of malignant kidney tumor and is responsible for 14,830 deaths per year in the United States. Among the four most common subtypes of renal cell carcinoma, clear cell renal cell carcinoma has the worst prognosis and clear cell papillary renal cell carcinoma appears to have no malignant potential. Distinction between these two subtypes can be difficult due to morphologic overlap on examination of histopathological preparation stained with hematoxylin and eosin. Ancillary techniques, such as immunohistochemistry, can be helpful, but they are not universally available. We propose and evaluate a new deep learning framework for tumor classification tasks to distinguish clear cell renal cell carcinoma from papillary renal cell carcinoma. METHODS: Our deep learning framework is composed of three convolutional neural networks. We divided whole-slide kidney images into patches with three different sizes where each network processes a specific patch size. Our framework provides patchwise and pixelwise classification. The histopathological kidney data is composed of 64 image slides that belong to 4 categories: fat, parenchyma, clear cell renal cell carcinoma, and clear cell papillary renal cell carcinoma. The final output of our framework is an image map where each pixel is classified into one class. To maintain consistency, we processed the map with Gauss-Markov random field smoothing. RESULTS: Our framework succeeded in classifying the four classes and showed superior performance compared to well-established state-of-the-art methods (pixel accuracy: 0.89 ResNet18, 0.92 proposed). CONCLUSIONS: Deep learning techniques have a significant potential for cancer diagnosis. Elsevier 2022-04-18 /pmc/articles/PMC9576982/ /pubmed/36268061 http://dx.doi.org/10.1016/j.jpi.2022.100093 Text en © 2022 Association for Pathology Informatics. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Abdeltawab, Hisham A.
Khalifa, Fahmi A.
Ghazal, Mohammed A.
Cheng, Liang
El-Baz, Ayman S.
Gondim, Dibson D.
A deep learning framework for automated classification of histopathological kidney whole-slide images
title A deep learning framework for automated classification of histopathological kidney whole-slide images
title_full A deep learning framework for automated classification of histopathological kidney whole-slide images
title_fullStr A deep learning framework for automated classification of histopathological kidney whole-slide images
title_full_unstemmed A deep learning framework for automated classification of histopathological kidney whole-slide images
title_short A deep learning framework for automated classification of histopathological kidney whole-slide images
title_sort deep learning framework for automated classification of histopathological kidney whole-slide images
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576982/
https://www.ncbi.nlm.nih.gov/pubmed/36268061
http://dx.doi.org/10.1016/j.jpi.2022.100093
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