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Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning

SIMPLE SUMMARY: In recent years, the prostate cancer histopathological description proposed by Gleason has emerged as a universal standard used for disease diagnosis and progression. Recently, a grading scheme on a point scale is based on Gleason patterns. Current scores are highly dependent on the...

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Autores principales: Fogarty, Ryan, Goldgof, Dmitry, Hall, Lawrence, Lopez, Alex, Johnson, Joseph, Gadara, Manoj, Stoyanova, Radka, Punnen, Sanoj, Pollack, Alan, Pow-Sang, Julio, Balagurunathan, Yoganand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136774/
https://www.ncbi.nlm.nih.gov/pubmed/37190264
http://dx.doi.org/10.3390/cancers15082335
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author Fogarty, Ryan
Goldgof, Dmitry
Hall, Lawrence
Lopez, Alex
Johnson, Joseph
Gadara, Manoj
Stoyanova, Radka
Punnen, Sanoj
Pollack, Alan
Pow-Sang, Julio
Balagurunathan, Yoganand
author_facet Fogarty, Ryan
Goldgof, Dmitry
Hall, Lawrence
Lopez, Alex
Johnson, Joseph
Gadara, Manoj
Stoyanova, Radka
Punnen, Sanoj
Pollack, Alan
Pow-Sang, Julio
Balagurunathan, Yoganand
author_sort Fogarty, Ryan
collection PubMed
description SIMPLE SUMMARY: In recent years, the prostate cancer histopathological description proposed by Gleason has emerged as a universal standard used for disease diagnosis and progression. Recently, a grading scheme on a point scale is based on Gleason patterns. Current scores are highly dependent on the expert urinary histopathologist and show a high level of variability among experts. To aid the clinician, we have developed deep learning models that provide a decision aid in identifying the primary cancer grade (dominant Gleason pattern). ABSTRACT: Histopathological classification in prostate cancer remains a challenge with high dependence on the expert practitioner. We develop a deep learning (DL) model to identify the most prominent Gleason pattern in a highly curated data cohort and validate it on an independent dataset. The histology images are partitioned in tiles (14,509) and are curated by an expert to identify individual glandular structures with assigned primary Gleason pattern grades. We use transfer learning and fine-tuning approaches to compare several deep neural network architectures that are trained on a corpus of camera images (ImageNet) and tuned with histology examples to be context appropriate for histopathological discrimination with small samples. In our study, the best DL network is able to discriminate cancer grade (GS3/4) from benign with an accuracy of 91%, F(1)-score of 0.91 and AUC 0.96 in a baseline test (52 patients), while the cancer grade discrimination of the GS3 from GS4 had an accuracy of 68% and AUC of 0.71 (40 patients).
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spelling pubmed-101367742023-04-28 Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning Fogarty, Ryan Goldgof, Dmitry Hall, Lawrence Lopez, Alex Johnson, Joseph Gadara, Manoj Stoyanova, Radka Punnen, Sanoj Pollack, Alan Pow-Sang, Julio Balagurunathan, Yoganand Cancers (Basel) Article SIMPLE SUMMARY: In recent years, the prostate cancer histopathological description proposed by Gleason has emerged as a universal standard used for disease diagnosis and progression. Recently, a grading scheme on a point scale is based on Gleason patterns. Current scores are highly dependent on the expert urinary histopathologist and show a high level of variability among experts. To aid the clinician, we have developed deep learning models that provide a decision aid in identifying the primary cancer grade (dominant Gleason pattern). ABSTRACT: Histopathological classification in prostate cancer remains a challenge with high dependence on the expert practitioner. We develop a deep learning (DL) model to identify the most prominent Gleason pattern in a highly curated data cohort and validate it on an independent dataset. The histology images are partitioned in tiles (14,509) and are curated by an expert to identify individual glandular structures with assigned primary Gleason pattern grades. We use transfer learning and fine-tuning approaches to compare several deep neural network architectures that are trained on a corpus of camera images (ImageNet) and tuned with histology examples to be context appropriate for histopathological discrimination with small samples. In our study, the best DL network is able to discriminate cancer grade (GS3/4) from benign with an accuracy of 91%, F(1)-score of 0.91 and AUC 0.96 in a baseline test (52 patients), while the cancer grade discrimination of the GS3 from GS4 had an accuracy of 68% and AUC of 0.71 (40 patients). MDPI 2023-04-17 /pmc/articles/PMC10136774/ /pubmed/37190264 http://dx.doi.org/10.3390/cancers15082335 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fogarty, Ryan
Goldgof, Dmitry
Hall, Lawrence
Lopez, Alex
Johnson, Joseph
Gadara, Manoj
Stoyanova, Radka
Punnen, Sanoj
Pollack, Alan
Pow-Sang, Julio
Balagurunathan, Yoganand
Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title_full Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title_fullStr Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title_full_unstemmed Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title_short Classifying Malignancy in Prostate Glandular Structures from Biopsy Scans with Deep Learning
title_sort classifying malignancy in prostate glandular structures from biopsy scans with deep learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136774/
https://www.ncbi.nlm.nih.gov/pubmed/37190264
http://dx.doi.org/10.3390/cancers15082335
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