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Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI

BACKGROUND: H3K27M mutation status significantly affects the prognosis of patients with diffuse midline gliomas (DMGs), but this tumor presents a high risk of pathological acquisition. We aimed to construct a fully automated model for predicting the H3K27M alteration status of DMGs based on deep lea...

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Autores principales: Huang, Bowen, Zhang, Yuekang, Mao, Qing, Ju, Yan, Liu, Yanhui, Su, Zhengzheng, Lei, Yinjie, Ren, Yanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501256/
https://www.ncbi.nlm.nih.gov/pubmed/37461358
http://dx.doi.org/10.1002/cam4.6363
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author Huang, Bowen
Zhang, Yuekang
Mao, Qing
Ju, Yan
Liu, Yanhui
Su, Zhengzheng
Lei, Yinjie
Ren, Yanming
author_facet Huang, Bowen
Zhang, Yuekang
Mao, Qing
Ju, Yan
Liu, Yanhui
Su, Zhengzheng
Lei, Yinjie
Ren, Yanming
author_sort Huang, Bowen
collection PubMed
description BACKGROUND: H3K27M mutation status significantly affects the prognosis of patients with diffuse midline gliomas (DMGs), but this tumor presents a high risk of pathological acquisition. We aimed to construct a fully automated model for predicting the H3K27M alteration status of DMGs based on deep learning using whole‐brain MRI. METHODS: DMG patients from West China Hospital of Sichuan University (WCHSU; n = 200) and Chengdu Shangjin Nanfu Hospital (CSNH; n = 35) who met the inclusion and exclusion criteria from February 2016 to April 2022 were enrolled as the training and external test sets, respectively. To adapt the model to the human head MRI scene, we use normal human head MR images to pretrain the model. The classification and tumor segmentation tasks are naturally related, so we conducted cotraining for the two tasks to enable information interaction between them and improve the accuracy of the classification task. RESULTS: The average classification accuracies of our model on the training and external test sets was 90.5% and 85.1%, respectively. Ablation experiments showed that pretraining and cotraining could improve the prediction accuracy and generalization performance of the model. In the training and external test sets, the average areas under the receiver operating characteristic curve (AUROCs) were 94.18% and 87.64%, and the average areas under the precision‐recall curve (AUPRC) were 93.26% and 85.4%. CONCLUSIONS: The developed model achieved excellent performance in predicting the H3K27M alteration status in DMGs, and its good reproducibility and generalization were verified in the external dataset.
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spelling pubmed-105012562023-09-15 Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI Huang, Bowen Zhang, Yuekang Mao, Qing Ju, Yan Liu, Yanhui Su, Zhengzheng Lei, Yinjie Ren, Yanming Cancer Med RESEARCH ARTICLES BACKGROUND: H3K27M mutation status significantly affects the prognosis of patients with diffuse midline gliomas (DMGs), but this tumor presents a high risk of pathological acquisition. We aimed to construct a fully automated model for predicting the H3K27M alteration status of DMGs based on deep learning using whole‐brain MRI. METHODS: DMG patients from West China Hospital of Sichuan University (WCHSU; n = 200) and Chengdu Shangjin Nanfu Hospital (CSNH; n = 35) who met the inclusion and exclusion criteria from February 2016 to April 2022 were enrolled as the training and external test sets, respectively. To adapt the model to the human head MRI scene, we use normal human head MR images to pretrain the model. The classification and tumor segmentation tasks are naturally related, so we conducted cotraining for the two tasks to enable information interaction between them and improve the accuracy of the classification task. RESULTS: The average classification accuracies of our model on the training and external test sets was 90.5% and 85.1%, respectively. Ablation experiments showed that pretraining and cotraining could improve the prediction accuracy and generalization performance of the model. In the training and external test sets, the average areas under the receiver operating characteristic curve (AUROCs) were 94.18% and 87.64%, and the average areas under the precision‐recall curve (AUPRC) were 93.26% and 85.4%. CONCLUSIONS: The developed model achieved excellent performance in predicting the H3K27M alteration status in DMGs, and its good reproducibility and generalization were verified in the external dataset. John Wiley and Sons Inc. 2023-07-17 /pmc/articles/PMC10501256/ /pubmed/37461358 http://dx.doi.org/10.1002/cam4.6363 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Huang, Bowen
Zhang, Yuekang
Mao, Qing
Ju, Yan
Liu, Yanhui
Su, Zhengzheng
Lei, Yinjie
Ren, Yanming
Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title_full Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title_fullStr Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title_full_unstemmed Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title_short Deep learning‐based prediction of H3K27M alteration in diffuse midline gliomas based on whole‐brain MRI
title_sort deep learning‐based prediction of h3k27m alteration in diffuse midline gliomas based on whole‐brain mri
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501256/
https://www.ncbi.nlm.nih.gov/pubmed/37461358
http://dx.doi.org/10.1002/cam4.6363
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