Deep Learning for Noninvasive Assessment of H3 K27M Mutation Status in Diffuse Midline Gliomas Using MR Imaging
Year: 2023
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Determination of H3 K27M mutation in diffuse midline glioma (DMG) is key for prognostic assessment and stratifying patient subgroups for clinical trials. MRI can noninvasively depict morphological and metabolic characteristics of H3 K27M mutant DMG. PURPOSE: This study aimed to develop a deep learning (DL) approach to noninvasively predict H3 K27M mutation in DMG using T2-weighted images. STUDY TYPE: Retrospective and prospective. POPULATION: For diffuse midline brain gliomas, 341 patients from Center-1 (27 ± 19 years, 184 males), 42 patients from Center-2 (33 ± 19 years, 27 males) and 35 patients (37 ± 18 years, 24 males). For diffuse spinal cord gliomas, 133 patients from Center-1 (30 ± 15 years, 80 males). FIELD STRENGTH/SEQUENCE: 5T and 3T, T2-weighted turbo spin echo imaging. ASSESSMENT: Conventional radiological features were independently reviewed by two neuroradiologists. H3 K27M status was determined by histopathological examination. The Dice coefficient was used to evaluate segmentation performance. Classification performance was evaluated using accuracy, sensitivity, specificity, and area under the curve. STATISTICAL TESTS: Pearson's Chi-squared test, Fisher's exact test, two-sample Student's t-test and Mann-Whitney U test. A two-sided P value <0.05 was considered statistically significant. RESULTS: In the testing cohort, Dice coefficients of tumor segmentation using DL were 0.87 for diffuse midline brain and 0.81 for spinal cord gliomas. In the internal prospective testing dataset, the predictive accuracies, sensitivities, and specificities of H3 K27M mutation status were 92.1%, 98.2%, 82.9% in diffuse midline brain gliomas and 85.4%, 88.9%, 82.6% in spinal cord gliomas. Furthermore, this study showed that the performance generalizes to external institutions, with predictive accuracies of 85.7%-90.5%, sensitivities of 90.9%-96.0%, and specificities of 82.4%-83.3%. DATA CONCLUSION: In this study, an automatic DL framework was developed and validated for accurately predicting H3 K27M mutation using T2-weighted images, which could contribute to the noninvasive determination of H3 K27M status for clinical decision-making. EVIDENCE LEVEL: 2 Technical Efficacy: Stage 2.
DOI: 10.1002/jmri.28606
Authors: Junjie Li, Peng Zhang, Liying Qu, Ting Sun, Yunyun Duan, Minghao Wu, Jinyuan Weng, Zhaohui Li, Xiaodong Gong, Xing Liu, Yongzhi Wang, Wenqing Jia, Xiaorui Su, Qiang Yue, Jianrui Li, Zhiqiang Zhang, Frederik Barkhof, Raymond Y. Huang, Ken Chang, Haris Sair, Chuyang Ye, Liwei Zhang, Zhizheng Zhuo, Yaou Liu
Institutions: Capital Medical University, Nanjing General Hospital of Nanjing Military Command, Beijing Tian Tan Hospital, Nanjing University, Neusoft (China), Neusoft Medical Systems Co., Ltd. (China), West China Hospital of Sichuan University, Amsterdam University Medical Centers, University College London, Brigham and Women's Hospital, Harvard University, Massachusetts General Hospital, Athinoula A. Martinos Center for Biomedical Imaging, Johns Hopkins University, Johns Hopkins Medicine, Beijing Institute of Technology
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G4375868633, G5664034357
OpenAlex ID: W4317869588
