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Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning
BACKGROUND: To evaluate the performances of multiparametric MRI‐based convolutional neural networks (CNNs) for the preoperative assessment of breast cancer molecular subtypes. METHODS: A total of 136 patients with 136 pathologically confirmed invasive breast cancers were randomly divided into traini...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663668/ https://www.ncbi.nlm.nih.gov/pubmed/36203226 http://dx.doi.org/10.1111/1759-7714.14673 |
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author | Yin, Haolin Bai, Lutian Jia, Huihui Lin, Guangwu |
author_facet | Yin, Haolin Bai, Lutian Jia, Huihui Lin, Guangwu |
author_sort | Yin, Haolin |
collection | PubMed |
description | BACKGROUND: To evaluate the performances of multiparametric MRI‐based convolutional neural networks (CNNs) for the preoperative assessment of breast cancer molecular subtypes. METHODS: A total of 136 patients with 136 pathologically confirmed invasive breast cancers were randomly divided into training, validation, and testing sets in this retrospective study. The CNN models were established based on contrast‐enhanced T(1)‐weighted imaging (T(1)C), Apparent diffusion coefficient (ADC), and T(2)‐weighted imaging (T(2)W) using the training and validation sets. The performances of CNN models were evaluated on the testing set. The area under the receiver operating characteristic curve (AUC), sensitivity, specificity, and accuracy were calculated to assess the performance. RESULTS: For the separation of each subtype from other subtypes on the testing set, the T(1)C‐based models yielded AUCs from 0.762 to 0.920; the ADC‐based models yielded AUCs from 0.686 to 0.851; and the T(2)W‐based models achieved AUCs from 0.639 to 0.697. CONCLUSION: T(1)C‐based models performed better than ADC‐based models and T(2)W‐based models in assessing the breast cancer molecular subtypes. The discriminating performances of our CNN models for triple negative and human epidermal growth factor receptor 2‐enriched subtypes were better than that of luminal A and luminal B subtypes. |
format | Online Article Text |
id | pubmed-9663668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-96636682022-11-16 Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning Yin, Haolin Bai, Lutian Jia, Huihui Lin, Guangwu Thorac Cancer Original Articles BACKGROUND: To evaluate the performances of multiparametric MRI‐based convolutional neural networks (CNNs) for the preoperative assessment of breast cancer molecular subtypes. METHODS: A total of 136 patients with 136 pathologically confirmed invasive breast cancers were randomly divided into training, validation, and testing sets in this retrospective study. The CNN models were established based on contrast‐enhanced T(1)‐weighted imaging (T(1)C), Apparent diffusion coefficient (ADC), and T(2)‐weighted imaging (T(2)W) using the training and validation sets. The performances of CNN models were evaluated on the testing set. The area under the receiver operating characteristic curve (AUC), sensitivity, specificity, and accuracy were calculated to assess the performance. RESULTS: For the separation of each subtype from other subtypes on the testing set, the T(1)C‐based models yielded AUCs from 0.762 to 0.920; the ADC‐based models yielded AUCs from 0.686 to 0.851; and the T(2)W‐based models achieved AUCs from 0.639 to 0.697. CONCLUSION: T(1)C‐based models performed better than ADC‐based models and T(2)W‐based models in assessing the breast cancer molecular subtypes. The discriminating performances of our CNN models for triple negative and human epidermal growth factor receptor 2‐enriched subtypes were better than that of luminal A and luminal B subtypes. John Wiley & Sons Australia, Ltd 2022-10-06 2022-11 /pmc/articles/PMC9663668/ /pubmed/36203226 http://dx.doi.org/10.1111/1759-7714.14673 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Yin, Haolin Bai, Lutian Jia, Huihui Lin, Guangwu Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title | Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title_full | Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title_fullStr | Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title_full_unstemmed | Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title_short | Noninvasive assessment of breast cancer molecular subtypes on multiparametric MRI using convolutional neural network with transfer learning |
title_sort | noninvasive assessment of breast cancer molecular subtypes on multiparametric mri using convolutional neural network with transfer learning |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663668/ https://www.ncbi.nlm.nih.gov/pubmed/36203226 http://dx.doi.org/10.1111/1759-7714.14673 |
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