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Automated classification of polyps using deep learning architectures and few-shot learning
BACKGROUND: Colorectal cancer is a leading cause of cancer-related deaths worldwide. The best method to prevent CRC is a colonoscopy. However, not all colon polyps have the risk of becoming cancerous. Therefore, polyps are classified using different classification systems. After the classification,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120204/ https://www.ncbi.nlm.nih.gov/pubmed/37081495 http://dx.doi.org/10.1186/s12880-023-01007-4 |
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author | Krenzer, Adrian Heil, Stefan Fitting, Daniel Matti, Safa Zoller, Wolfram G. Hann, Alexander Puppe, Frank |
author_facet | Krenzer, Adrian Heil, Stefan Fitting, Daniel Matti, Safa Zoller, Wolfram G. Hann, Alexander Puppe, Frank |
author_sort | Krenzer, Adrian |
collection | PubMed |
description | BACKGROUND: Colorectal cancer is a leading cause of cancer-related deaths worldwide. The best method to prevent CRC is a colonoscopy. However, not all colon polyps have the risk of becoming cancerous. Therefore, polyps are classified using different classification systems. After the classification, further treatment and procedures are based on the classification of the polyp. Nevertheless, classification is not easy. Therefore, we suggest two novel automated classifications system assisting gastroenterologists in classifying polyps based on the NICE and Paris classification. METHODS: We build two classification systems. One is classifying polyps based on their shape (Paris). The other classifies polyps based on their texture and surface patterns (NICE). A two-step process for the Paris classification is introduced: First, detecting and cropping the polyp on the image, and secondly, classifying the polyp based on the cropped area with a transformer network. For the NICE classification, we design a few-shot learning algorithm based on the Deep Metric Learning approach. The algorithm creates an embedding space for polyps, which allows classification from a few examples to account for the data scarcity of NICE annotated images in our database. RESULTS: For the Paris classification, we achieve an accuracy of 89.35 %, surpassing all papers in the literature and establishing a new state-of-the-art and baseline accuracy for other publications on a public data set. For the NICE classification, we achieve a competitive accuracy of 81.13 % and demonstrate thereby the viability of the few-shot learning paradigm in polyp classification in data-scarce environments. Additionally, we show different ablations of the algorithms. Finally, we further elaborate on the explainability of the system by showing heat maps of the neural network explaining neural activations. CONCLUSION: Overall we introduce two polyp classification systems to assist gastroenterologists. We achieve state-of-the-art performance in the Paris classification and demonstrate the viability of the few-shot learning paradigm in the NICE classification, addressing the prevalent data scarcity issues faced in medical machine learning. |
format | Online Article Text |
id | pubmed-10120204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101202042023-04-22 Automated classification of polyps using deep learning architectures and few-shot learning Krenzer, Adrian Heil, Stefan Fitting, Daniel Matti, Safa Zoller, Wolfram G. Hann, Alexander Puppe, Frank BMC Med Imaging Research BACKGROUND: Colorectal cancer is a leading cause of cancer-related deaths worldwide. The best method to prevent CRC is a colonoscopy. However, not all colon polyps have the risk of becoming cancerous. Therefore, polyps are classified using different classification systems. After the classification, further treatment and procedures are based on the classification of the polyp. Nevertheless, classification is not easy. Therefore, we suggest two novel automated classifications system assisting gastroenterologists in classifying polyps based on the NICE and Paris classification. METHODS: We build two classification systems. One is classifying polyps based on their shape (Paris). The other classifies polyps based on their texture and surface patterns (NICE). A two-step process for the Paris classification is introduced: First, detecting and cropping the polyp on the image, and secondly, classifying the polyp based on the cropped area with a transformer network. For the NICE classification, we design a few-shot learning algorithm based on the Deep Metric Learning approach. The algorithm creates an embedding space for polyps, which allows classification from a few examples to account for the data scarcity of NICE annotated images in our database. RESULTS: For the Paris classification, we achieve an accuracy of 89.35 %, surpassing all papers in the literature and establishing a new state-of-the-art and baseline accuracy for other publications on a public data set. For the NICE classification, we achieve a competitive accuracy of 81.13 % and demonstrate thereby the viability of the few-shot learning paradigm in polyp classification in data-scarce environments. Additionally, we show different ablations of the algorithms. Finally, we further elaborate on the explainability of the system by showing heat maps of the neural network explaining neural activations. CONCLUSION: Overall we introduce two polyp classification systems to assist gastroenterologists. We achieve state-of-the-art performance in the Paris classification and demonstrate the viability of the few-shot learning paradigm in the NICE classification, addressing the prevalent data scarcity issues faced in medical machine learning. BioMed Central 2023-04-20 /pmc/articles/PMC10120204/ /pubmed/37081495 http://dx.doi.org/10.1186/s12880-023-01007-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Krenzer, Adrian Heil, Stefan Fitting, Daniel Matti, Safa Zoller, Wolfram G. Hann, Alexander Puppe, Frank Automated classification of polyps using deep learning architectures and few-shot learning |
title | Automated classification of polyps using deep learning architectures and few-shot learning |
title_full | Automated classification of polyps using deep learning architectures and few-shot learning |
title_fullStr | Automated classification of polyps using deep learning architectures and few-shot learning |
title_full_unstemmed | Automated classification of polyps using deep learning architectures and few-shot learning |
title_short | Automated classification of polyps using deep learning architectures and few-shot learning |
title_sort | automated classification of polyps using deep learning architectures and few-shot learning |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120204/ https://www.ncbi.nlm.nih.gov/pubmed/37081495 http://dx.doi.org/10.1186/s12880-023-01007-4 |
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