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Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network

Identification of genotypes is crucial for treatment of glioma. Here, we developed a method to predict tumor genotypes using a pretrained convolutional neural network (CNN) from magnetic resonance (MR) images and compared the accuracy to that of a diagnosis based on conventional radiomic features an...

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Autores principales: Fukuma, Ryohei, Yanagisawa, Takufumi, Kinoshita, Manabu, Shinozaki, Takashi, Arita, Hideyuki, Kawaguchi, Atsushi, Takahashi, Masamichi, Narita, Yoshitaka, Terakawa, Yuzo, Tsuyuguchi, Naohiro, Okita, Yoshiko, Nonaka, Masahiro, Moriuchi, Shusuke, Takagaki, Masatoshi, Fujimoto, Yasunori, Fukai, Junya, Izumoto, Shuichi, Ishibashi, Kenichi, Nakajima, Yoshikazu, Shofuda, Tomoko, Kanematsu, Daisuke, Yoshioka, Ema, Kodama, Yoshinori, Mano, Masayuki, Mori, Kanji, Ichimura, Koichi, Kanemura, Yonehiro, Kishima, Haruhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937237/
https://www.ncbi.nlm.nih.gov/pubmed/31889117
http://dx.doi.org/10.1038/s41598-019-56767-3
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author Fukuma, Ryohei
Yanagisawa, Takufumi
Kinoshita, Manabu
Shinozaki, Takashi
Arita, Hideyuki
Kawaguchi, Atsushi
Takahashi, Masamichi
Narita, Yoshitaka
Terakawa, Yuzo
Tsuyuguchi, Naohiro
Okita, Yoshiko
Nonaka, Masahiro
Moriuchi, Shusuke
Takagaki, Masatoshi
Fujimoto, Yasunori
Fukai, Junya
Izumoto, Shuichi
Ishibashi, Kenichi
Nakajima, Yoshikazu
Shofuda, Tomoko
Kanematsu, Daisuke
Yoshioka, Ema
Kodama, Yoshinori
Mano, Masayuki
Mori, Kanji
Ichimura, Koichi
Kanemura, Yonehiro
Kishima, Haruhiko
author_facet Fukuma, Ryohei
Yanagisawa, Takufumi
Kinoshita, Manabu
Shinozaki, Takashi
Arita, Hideyuki
Kawaguchi, Atsushi
Takahashi, Masamichi
Narita, Yoshitaka
Terakawa, Yuzo
Tsuyuguchi, Naohiro
Okita, Yoshiko
Nonaka, Masahiro
Moriuchi, Shusuke
Takagaki, Masatoshi
Fujimoto, Yasunori
Fukai, Junya
Izumoto, Shuichi
Ishibashi, Kenichi
Nakajima, Yoshikazu
Shofuda, Tomoko
Kanematsu, Daisuke
Yoshioka, Ema
Kodama, Yoshinori
Mano, Masayuki
Mori, Kanji
Ichimura, Koichi
Kanemura, Yonehiro
Kishima, Haruhiko
author_sort Fukuma, Ryohei
collection PubMed
description Identification of genotypes is crucial for treatment of glioma. Here, we developed a method to predict tumor genotypes using a pretrained convolutional neural network (CNN) from magnetic resonance (MR) images and compared the accuracy to that of a diagnosis based on conventional radiomic features and patient age. Multisite preoperative MR images of 164 patients with grade II/III glioma were grouped by IDH and TERT promoter (pTERT) mutations as follows: (1) IDH wild type, (2) IDH and pTERT co-mutations, (3) IDH mutant and pTERT wild type. We applied a CNN (AlexNet) to four types of MR sequence and obtained the CNN texture features to classify the groups with a linear support vector machine. The classification was also performed using conventional radiomic features and/or patient age. Using all features, we succeeded in classifying patients with an accuracy of 63.1%, which was significantly higher than the accuracy obtained from using either the radiomic features or patient age alone. In particular, prediction of the pTERT mutation was significantly improved by the CNN texture features. In conclusion, the pretrained CNN texture features capture the information of IDH and TERT genotypes in grade II/III gliomas better than the conventional radiomic features.
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spelling pubmed-69372372020-01-06 Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network Fukuma, Ryohei Yanagisawa, Takufumi Kinoshita, Manabu Shinozaki, Takashi Arita, Hideyuki Kawaguchi, Atsushi Takahashi, Masamichi Narita, Yoshitaka Terakawa, Yuzo Tsuyuguchi, Naohiro Okita, Yoshiko Nonaka, Masahiro Moriuchi, Shusuke Takagaki, Masatoshi Fujimoto, Yasunori Fukai, Junya Izumoto, Shuichi Ishibashi, Kenichi Nakajima, Yoshikazu Shofuda, Tomoko Kanematsu, Daisuke Yoshioka, Ema Kodama, Yoshinori Mano, Masayuki Mori, Kanji Ichimura, Koichi Kanemura, Yonehiro Kishima, Haruhiko Sci Rep Article Identification of genotypes is crucial for treatment of glioma. Here, we developed a method to predict tumor genotypes using a pretrained convolutional neural network (CNN) from magnetic resonance (MR) images and compared the accuracy to that of a diagnosis based on conventional radiomic features and patient age. Multisite preoperative MR images of 164 patients with grade II/III glioma were grouped by IDH and TERT promoter (pTERT) mutations as follows: (1) IDH wild type, (2) IDH and pTERT co-mutations, (3) IDH mutant and pTERT wild type. We applied a CNN (AlexNet) to four types of MR sequence and obtained the CNN texture features to classify the groups with a linear support vector machine. The classification was also performed using conventional radiomic features and/or patient age. Using all features, we succeeded in classifying patients with an accuracy of 63.1%, which was significantly higher than the accuracy obtained from using either the radiomic features or patient age alone. In particular, prediction of the pTERT mutation was significantly improved by the CNN texture features. In conclusion, the pretrained CNN texture features capture the information of IDH and TERT genotypes in grade II/III gliomas better than the conventional radiomic features. Nature Publishing Group UK 2019-12-30 /pmc/articles/PMC6937237/ /pubmed/31889117 http://dx.doi.org/10.1038/s41598-019-56767-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fukuma, Ryohei
Yanagisawa, Takufumi
Kinoshita, Manabu
Shinozaki, Takashi
Arita, Hideyuki
Kawaguchi, Atsushi
Takahashi, Masamichi
Narita, Yoshitaka
Terakawa, Yuzo
Tsuyuguchi, Naohiro
Okita, Yoshiko
Nonaka, Masahiro
Moriuchi, Shusuke
Takagaki, Masatoshi
Fujimoto, Yasunori
Fukai, Junya
Izumoto, Shuichi
Ishibashi, Kenichi
Nakajima, Yoshikazu
Shofuda, Tomoko
Kanematsu, Daisuke
Yoshioka, Ema
Kodama, Yoshinori
Mano, Masayuki
Mori, Kanji
Ichimura, Koichi
Kanemura, Yonehiro
Kishima, Haruhiko
Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title_full Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title_fullStr Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title_full_unstemmed Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title_short Prediction of IDH and TERT promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
title_sort prediction of idh and tert promoter mutations in low-grade glioma from magnetic resonance images using a convolutional neural network
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937237/
https://www.ncbi.nlm.nih.gov/pubmed/31889117
http://dx.doi.org/10.1038/s41598-019-56767-3
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