利用成人型弥漫性胶质瘤MRI图像预测IDH突变和1p/19q编码的易于使用的机器学习系统。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2023-04-01 DOI:10.1007/s10014-023-00459-4
Tomohide Nishikawa, Fumiharu Ohka, Kosuke Aoki, Hiromichi Suzuki, Kazuya Motomura, Junya Yamaguchi, Sachi Maeda, Yuji Kibe, Hiroki Shimizu, Atsushi Natsume, Hideki Innan, Ryuta Saito
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引用次数: 1

摘要

成人型弥漫性胶质瘤分为星形细胞瘤、IDH突变型、少突胶质细胞瘤、IDH突变型和1p/19q编码缺失型、胶质母细胞瘤、IDH野生型(基于IDH突变)和1p/19q编码缺失状态。为了确定这些肿瘤的治疗策略,术前预测IDH突变和1p/19q编码状态可能是有效的。使用机器学习的计算机辅助诊断(CADx)系统被认为是一种创新的诊断方法。然而,由于各种专家的支持是必不可少的,因此很难在每个研究所推广机器学习系统的临床应用。在本研究中,我们使用Microsoft Azure Machine Learning Studio (MAMLS)建立了一个易于使用的计算机辅助诊断系统来预测这些状态。我们使用来自癌症基因组图谱(TCGA)队列的258例成人型弥漫性胶质瘤病例构建了一个分析模型。MRI t2加权图像预测IDH突变和1p/19q密码缺失的总体准确性、敏感性和特异性分别为86.9%、80.9%和92.0%,94.7%、94.1%和95.1%。我们还建立了一个可靠的分析模型,用于预测IDH突变和1p/19q密码缺失,使用独立的名古屋队列,包括202例。这些分析模型在30分钟内建立。这种易于使用的CADx系统可能有助于CADx在各个研究所的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Easy-to-use machine learning system for the prediction of IDH mutation and 1p/19q codeletion using MRI images of adult-type diffuse gliomas.

Adult-type diffuse gliomas are divided into Astrocytoma, IDH-mutant, Oligodendroglioma, IDH-mutant and 1p/19q-codeleted and Glioblastoma, IDH-wildtype based on the IDH mutation, and 1p/19q codeletion status. To determine the treatment strategy for these tumors, pre-operative prediction of IDH mutation and 1p/19q codeletion status might be effective. Computer-aided diagnosis (CADx) systems using machine learning have been noted as innovative diagnostic methods. However, it is difficult to promote the clinical application of machine learning systems at each institute because the support of various specialists is essential. In this study, we established an easy-to-use computer-aided diagnosis system using Microsoft Azure Machine Learning Studio (MAMLS) to predict these statuses. We constructed an analysis model using 258 adult-type diffuse glioma cases from The Cancer Genome Atlas (TCGA) cohort. Using MRI T2-weighted images, the overall accuracy, sensitivity, and specificity for the prediction of IDH mutation and 1p/19q codeletion were 86.9%, 80.9%, and 92.0%, and 94.7%, 94.1%, and 95.1%, respectively. We also constructed an reliable analysis model for the prediction of IDH mutation and 1p/19q codeletion using an independent Nagoya cohort including 202 cases. These analysis models were established within 30 min. This easy-to-use CADx system might be useful for the clinical application of CADx in various institutes.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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