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Added prognostic value of 3D deep learning-derived features from preoperative MRI for adult-type diffuse gliomas

Authors
 Jung Oh Lee  ;  Sung Soo Ahn  ;  Kyu Sung Choi  ;  Junhyeok Lee  ;  Joon Jang  ;  Jung Hyun Park  ;  Inpyeong Hwang  ;  Chul-Kee Park  ;  Sung Hye Park  ;  Jin Wook Chung  ;  Seung Hong Choi 
Citation
 NEURO-ONCOLOGY, Vol.26(3) : 571-580, 2024-03 
Journal Title
NEURO-ONCOLOGY
ISSN
 1522-8517 
Issue Date
2024-03
MeSH
Adult ; Brain Neoplasms* / diagnostic imaging ; Brain Neoplasms* / genetics ; Deep Learning* ; Glioma* / diagnostic imaging ; Glioma* / genetics ; Glioma* / surgery ; Humans ; Magnetic Resonance Imaging / methods ; Prognosis ; Retrospective Studies
Keywords
Deep learning ; Glioblastoma ; Isocitrate dehydrogenase ; Magnetic resonance imaging ; Survival analysis
Abstract
Background. To investigate the prognostic value of spatial features from whole-brain MRI using a three-dimensional (3D) convolutional neural network for adult-type diffuse gliomas. Methods. In a retrospective, multicenter study, 1925 diffuse glioma patients were enrolled from 5 datasets: SNUH (n = 708), UPenn (n = 425), UCSF (n = 500), TCGA (n = 160), and Severance (n = 132). The SNUH and Severance datasets served as external test sets. Precontrast and postcontrast 3D T1-weighted, T2-weighted, and T2-FLAIR images were processed as multichannel 3D images. A 3D-adapted SE-ResNeXt model was trained to predict overall survival. The prognostic value of the deep learning-based prognostic index (DPI), a spatial feature-derived quantitative score, and established prognostic markers were evaluated using Cox regression. Model evaluation was performed using the concordance index (C-index) and Brier score. Results: The MRI-only median DPI survival prediction model achieved C-indices of 0.709 and 0.677 (BS = 0.142 and 0.215) and survival differences (P < 0.001 and P = 0.002; log-rank test) for the SNUH and Severance datasets, respectively. Multivariate Cox analysis revealed DPI as a significant prognostic factor, independent of clinical and molecular genetic variables: hazard ratio = 0.032 and 0.036 (P < 0.001 and P = 0.004) for the SNUH and Severance datasets, respectively. Multimodal prediction models achieved higher C-indices than models using only clinical and molecular genetic variables: 0.783 vs. 0.774, P = 0.001, SNUH; 0.766 vs. 0.748, P = 0.023, Severance. Conclusions: The global morphologic feature derived from 3D CNN models using whole-brain MRI has independent prognostic value for diffuse gliomas. Combining clinical, molecular genetic, and imaging data yields the best performance. © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.
Full Text
https://academic.oup.com/neuro-oncology/article/26/3/571/7322058
DOI
10.1093/neuonc/noad202
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
Yonsei Authors
Ahn, Sung Soo(안성수) ORCID logo https://orcid.org/0000-0002-0503-5558
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/199204
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