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Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma

OBJECTIVE: The purpose of this study was to develop a deep learning-based system to automatically predict epidermal growth factor receptor (EGFR) mutant lung adenocarcinoma in (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT). METHODS: Three hundred and one lun...

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Autores principales: Yin, Guotao, Wang, Ziyang, Song, Yingchao, Li, Xiaofeng, Chen, Yiwen, Zhu, Lei, Su, Qian, Dai, Dong, Xu, Wengui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340023/
https://www.ncbi.nlm.nih.gov/pubmed/34367993
http://dx.doi.org/10.3389/fonc.2021.709137
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author Yin, Guotao
Wang, Ziyang
Song, Yingchao
Li, Xiaofeng
Chen, Yiwen
Zhu, Lei
Su, Qian
Dai, Dong
Xu, Wengui
author_facet Yin, Guotao
Wang, Ziyang
Song, Yingchao
Li, Xiaofeng
Chen, Yiwen
Zhu, Lei
Su, Qian
Dai, Dong
Xu, Wengui
author_sort Yin, Guotao
collection PubMed
description OBJECTIVE: The purpose of this study was to develop a deep learning-based system to automatically predict epidermal growth factor receptor (EGFR) mutant lung adenocarcinoma in (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT). METHODS: Three hundred and one lung adenocarcinoma patients with EGFR mutation status were enrolled in this study. Two deep learning models (SE(CT) and SE(PET)) were developed with Squeeze-and-Excitation Residual Network (SE-ResNet) module for the prediction of EGFR mutation with CT and PET images, respectively. The deep learning models were trained with a training data set of 198 patients and tested with a testing data set of 103 patients. Stacked generalization was used to integrate the results of SE(CT) and SE(PET). RESULTS: The AUCs of the SE(CT) and SE(PET) were 0.72 (95% CI, 0.62–0.80) and 0.74 (95% CI, 0.65–0.82) in the testing data set, respectively. After integrating SE(CT) and SE(PET) with stacked generalization, the AUC was further improved to 0.84 (95% CI, 0.75–0.90), significantly higher than SE(CT) (p<0.05). CONCLUSION: The stacking model based on (18)F-FDG PET/CT images is capable to predict EGFR mutation status of patients with lung adenocarcinoma automatically and non-invasively. The proposed model in this study showed the potential to help clinicians identify suitable advanced patients with lung adenocarcinoma for EGFR‐targeted therapy.
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spelling pubmed-83400232021-08-06 Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma Yin, Guotao Wang, Ziyang Song, Yingchao Li, Xiaofeng Chen, Yiwen Zhu, Lei Su, Qian Dai, Dong Xu, Wengui Front Oncol Oncology OBJECTIVE: The purpose of this study was to develop a deep learning-based system to automatically predict epidermal growth factor receptor (EGFR) mutant lung adenocarcinoma in (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT). METHODS: Three hundred and one lung adenocarcinoma patients with EGFR mutation status were enrolled in this study. Two deep learning models (SE(CT) and SE(PET)) were developed with Squeeze-and-Excitation Residual Network (SE-ResNet) module for the prediction of EGFR mutation with CT and PET images, respectively. The deep learning models were trained with a training data set of 198 patients and tested with a testing data set of 103 patients. Stacked generalization was used to integrate the results of SE(CT) and SE(PET). RESULTS: The AUCs of the SE(CT) and SE(PET) were 0.72 (95% CI, 0.62–0.80) and 0.74 (95% CI, 0.65–0.82) in the testing data set, respectively. After integrating SE(CT) and SE(PET) with stacked generalization, the AUC was further improved to 0.84 (95% CI, 0.75–0.90), significantly higher than SE(CT) (p<0.05). CONCLUSION: The stacking model based on (18)F-FDG PET/CT images is capable to predict EGFR mutation status of patients with lung adenocarcinoma automatically and non-invasively. The proposed model in this study showed the potential to help clinicians identify suitable advanced patients with lung adenocarcinoma for EGFR‐targeted therapy. Frontiers Media S.A. 2021-07-22 /pmc/articles/PMC8340023/ /pubmed/34367993 http://dx.doi.org/10.3389/fonc.2021.709137 Text en Copyright © 2021 Yin, Wang, Song, Li, Chen, Zhu, Su, Dai and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Yin, Guotao
Wang, Ziyang
Song, Yingchao
Li, Xiaofeng
Chen, Yiwen
Zhu, Lei
Su, Qian
Dai, Dong
Xu, Wengui
Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title_full Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title_fullStr Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title_full_unstemmed Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title_short Prediction of EGFR Mutation Status Based on (18)F-FDG PET/CT Imaging Using Deep Learning-Based Model in Lung Adenocarcinoma
title_sort prediction of egfr mutation status based on (18)f-fdg pet/ct imaging using deep learning-based model in lung adenocarcinoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340023/
https://www.ncbi.nlm.nih.gov/pubmed/34367993
http://dx.doi.org/10.3389/fonc.2021.709137
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