<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Akbari H</submitter><funding>BLRD VA</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1102-1115</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12083074</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Glioblastoma (GBM) is the most aggressive adult primary brain cancer, characterized by significant heterogeneity, posing challenges for patient management, treatment planning, and clinical trial stratification.&lt;h4>Methods&lt;/h4>We developed a highly reproducible, personalized prognostication, and clinical subgrouping system using machine learning (ML) on routine clinical data, magnetic resonance imaging (MRI), and molecular measures from 2838 demographically diverse patients across 22 institutions and 3 continents. Patients were stratified into favorable, intermediate, and poor prognostic subgroups (I, II, and III) using Kaplan-Meier analysis (Cox proportional model and hazard ratios [HR]).&lt;h4>Results&lt;/h4>The ML model stratified patients into distinct prognostic subgroups </pubmed_abstract><journal>Neuro-oncology</journal><pubmed_title>Machine learning-based prognostic subgrouping of glioblastoma: A multicenter study.</pubmed_title><pmcid>PMC12083074</pmcid><funding_grant_id>R01CA269948</funding_grant_id><funding_grant_id>I01 BX005842</funding_grant_id><funding_grant_id>U24CA189523</funding_grant_id><funding_grant_id>U24 CA189523</funding_grant_id><funding_grant_id>R01 CA269948</funding_grant_id><funding_grant_id>R01 CA264017</funding_grant_id><funding_grant_id>R01 CA277728</funding_grant_id><funding_grant_id>U01CA242871</funding_grant_id><funding_grant_id>U01 CA242871</funding_grant_id><pubmed_authors>Park YW</pubmed_authors><pubmed_authors>Satgunaseelan L</pubmed_authors><pubmed_authors>Akbari H</pubmed_authors><pubmed_authors>Vadmal V</pubmed_authors><pubmed_authors>Fathallah-Shaykh H</pubmed_authors><pubmed_authors>Shi W</pubmed_authors><pubmed_authors>Di Stefano AL</pubmed_authors><pubmed_authors>LaMontagne P</pubmed_authors><pubmed_authors>Marcus DS</pubmed_authors><pubmed_authors>Desai AS</pubmed_authors><pubmed_authors>Davatzikos C</pubmed_authors><pubmed_authors>Mahajan A</pubmed_authors><pubmed_authors>Bagley SJ</pubmed_authors><pubmed_authors>Mohan S</pubmed_authors><pubmed_authors>Ali AS</pubmed_authors><pubmed_authors>Nazeri A</pubmed_authors><pubmed_authors>Kotrotsou A</pubmed_authors><pubmed_authors>Villanueva-Meyer J</pubmed_authors><pubmed_authors>Jain R</pubmed_authors><pubmed_authors>Bakas S</pubmed_authors><pubmed_authors>Bilello M</pubmed_authors><pubmed_authors>Tiwari P</pubmed_authors><pubmed_authors>Prior T</pubmed_authors><pubmed_authors>Shinohara RT</pubmed_authors><pubmed_authors>Nasrallah MP</pubmed_authors><pubmed_authors>ReSPOND consortium</pubmed_authors><pubmed_authors>Barnholtz-Sloan JS</pubmed_authors><pubmed_authors>Rulseh AM</pubmed_authors><pubmed_authors>Rogers LR</pubmed_authors><pubmed_authors>Sotiras A</pubmed_authors><pubmed_authors>Chang JH</pubmed_authors><pubmed_authors>Sloan AE</pubmed_authors><pubmed_authors>Balana C</pubmed_authors><pubmed_authors>Melhem ER</pubmed_authors><pubmed_authors>Otani Y</pubmed_authors><pubmed_authors>Griffith B</pubmed_authors><pubmed_authors>Valdes P</pubmed_authors><pubmed_authors>Choi YS</pubmed_authors><pubmed_authors>Dicker AP</pubmed_authors><pubmed_authors>Kurozumi K</pubmed_authors><pubmed_authors>Rudie J</pubmed_authors><pubmed_authors>Maloney E</pubmed_authors><pubmed_authors>Garcia JA</pubmed_authors><pubmed_authors>Cepeda S</pubmed_authors><pubmed_authors>Lee M</pubmed_authors><pubmed_authors>Baid U</pubmed_authors><pubmed_authors>Puig J</pubmed_authors><pubmed_authors>Woodworth GF</pubmed_authors><pubmed_authors>Alexander GS</pubmed_authors><pubmed_authors>Alexander K</pubmed_authors><pubmed_authors>Ahn SS</pubmed_authors><pubmed_authors>Waite K</pubmed_authors><pubmed_authors>Aboian M</pubmed_authors><pubmed_authors>Sako C</pubmed_authors><pubmed_authors>Brem S</pubmed_authors><pubmed_authors>Liem S</pubmed_authors><pubmed_authors>Koizumi S</pubmed_authors><pubmed_authors>Shukla G</pubmed_authors><pubmed_authors>Imoto R</pubmed_authors><pubmed_authors>Lee SK</pubmed_authors><pubmed_authors>Chakravarti A</pubmed_authors><pubmed_authors>Palmer JD</pubmed_authors><pubmed_authors>Booth TC</pubmed_authors><pubmed_authors>Getka A</pubmed_authors><pubmed_authors>Lombardo J</pubmed_authors><pubmed_authors>Ak M</pubmed_authors><pubmed_authors>Binder ZA</pubmed_authors><pubmed_authors>Pati S</pubmed_authors><pubmed_authors>Singh A</pubmed_authors><pubmed_authors>Matsumoto Y</pubmed_authors><pubmed_authors>Chang S</pubmed_authors><pubmed_authors>Poisson LM</pubmed_authors><pubmed_authors>Badve C</pubmed_authors><pubmed_authors>Capellades J</pubmed_authors><pubmed_authors>Milchenko M</pubmed_authors><pubmed_authors>DiCostanzo D</pubmed_authors><pubmed_authors>Mamourian E</pubmed_authors><pubmed_authors>Calabrese E</pubmed_authors><pubmed_authors>Santonocito OS</pubmed_authors><pubmed_authors>Lustig RA</pubmed_authors><pubmed_authors>Amankulor N</pubmed_authors><pubmed_authors>Colen RR</pubmed_authors><pubmed_authors>Flanders AE</pubmed_authors><pubmed_authors>O'Rourke DM</pubmed_authors><pubmed_authors>Wiestler B</pubmed_authors><pubmed_authors>Kawakatsu T</pubmed_authors><pubmed_authors>Liu F</pubmed_authors><pubmed_authors>Fathi Kazerooni A</pubmed_authors><pubmed_authors>Cao Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Machine learning-based prognostic subgrouping of glioblastoma: A multicenter study.</name><description>&lt;h4>Background&lt;/h4>Glioblastoma (GBM) is the most aggressive adult primary brain cancer, characterized by significant heterogeneity, posing challenges for patient management, treatment planning, and clinical trial stratification.&lt;h4>Methods&lt;/h4>We developed a highly reproducible, personalized prognostication, and clinical subgrouping system using machine learning (ML) on routine clinical data, magnetic resonance imaging (MRI), and molecular measures from 2838 demographically diverse patients across 22 institutions and 3 continents. Patients were stratified into favorable, intermediate, and poor prognostic subgroups (I, II, and III) using Kaplan-Meier analysis (Cox proportional model and hazard ratios [HR]).&lt;h4>Results&lt;/h4>The ML model stratified patients into distinct prognostic subgroups </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-06-10T05:17:54.618Z</modification><creation>2026-06-10T03:07:29.411Z</creation></dates><accession>S-EPMC12083074</accession><cross_references><pubmed>39665363</pubmed><doi>10.1093/neuonc/noae260</doi></cross_references></HashMap>