<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee JO</submitter><funding>SNUH Research Fund</funding><funding>SPST</funding><pagination>571-580</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10912011</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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 &lt; 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 &lt; 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.&lt;h4>Conclusions&lt;/h4>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.</pubmed_abstract><journal>Neuro-oncology</journal><pubmed_title>Added prognostic value of 3D deep learning-derived features from preoperative MRI for adult-type diffuse gliomas.</pubmed_title><pmcid>PMC10912011</pmcid><funding_grant_id>04-2022-0520</funding_grant_id><pubmed_authors>Choi SH</pubmed_authors><pubmed_authors>Lee JO</pubmed_authors><pubmed_authors>Park JH</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Jang J</pubmed_authors><pubmed_authors>Park SH</pubmed_authors><pubmed_authors>Choi KS</pubmed_authors><pubmed_authors>Ahn SS</pubmed_authors><pubmed_authors>Park CK</pubmed_authors><pubmed_authors>Hwang I</pubmed_authors><pubmed_authors>Chung JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Added prognostic value of 3D deep learning-derived features from preoperative MRI for adult-type diffuse gliomas.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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 &lt; 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 &lt; 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.&lt;h4>Conclusions&lt;/h4>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.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-02T03:14:59.039Z</modification><creation>2025-04-04T00:34:47.142Z</creation></dates><accession>S-EPMC10912011</accession><cross_references><pubmed>37855826</pubmed><doi>10.1093/neuonc/noad202</doi></cross_references></HashMap>