<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Figarella-Branger D</submitter><funding>Institut National du Cancer</funding><pagination>755-766</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11889709</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>In the POLA cohort, 3 pathological groups of CNS WHO grade 3 oligodendroglioma IDH-mutant and 1p/19q co-deleted have been described: group 1 (high mitotic count only), group 2 (microvascular proliferation MVP and no necrosis), and group 3 (MVP and necrosis).&lt;h4>Methods&lt;/h4>494 patients from the POLA cohort, with a median follow-up of 96 months were included. To identify the impact of the pathological groups and contrast enhancement (CE) in group 1 on overall survival (OS) or progression-free survival (PFS), survival curves were obtained (Kaplan-Meier method) and compared (log-rank test). The prognostic value of clinical factors and CDKN2A homozygous deletion HD were also tested. Multivariate analysis was performed.&lt;h4>Results&lt;/h4>Survival analysis demonstrated that the p</pubmed_abstract><journal>Neuro-oncology</journal><pubmed_title>Reappraisal of prognostic factors in CNS WHO grade 3 oligodendrogliomas IDH-mutant and 1p/19q co-deleted: Lessons from the French POLA cohort.</pubmed_title><pmcid>PMC11889709</pmcid><funding_grant_id>INCa_16828</funding_grant_id><pubmed_authors>Appay R</pubmed_authors><pubmed_authors>Dehais C</pubmed_authors><pubmed_authors>Andraud M</pubmed_authors><pubmed_authors>Dhermain F</pubmed_authors><pubmed_authors>Mokhtari K</pubmed_authors><pubmed_authors>Seyve A</pubmed_authors><pubmed_authors>POLA network</pubmed_authors><pubmed_authors>Guillamo JS</pubmed_authors><pubmed_authors>Noel G</pubmed_authors><pubmed_authors>Cruel T</pubmed_authors><pubmed_authors>Adam C</pubmed_authors><pubmed_authors>Guillain N</pubmed_authors><pubmed_authors>Vandenbos-Burel F</pubmed_authors><pubmed_authors>Lhermitte B</pubmed_authors><pubmed_authors>Cohen-Moyal E</pubmed_authors><pubmed_authors>Marguet F</pubmed_authors><pubmed_authors>Forest F</pubmed_authors><pubmed_authors>Richard P</pubmed_authors><pubmed_authors>Younan N</pubmed_authors><pubmed_authors>Gaultier C</pubmed_authors><pubmed_authors>Desenclos C</pubmed_authors><pubmed_authors>Chiforeanu D</pubmed_authors><pubmed_authors>Rigau V</pubmed_authors><pubmed_authors>Rousseau A</pubmed_authors><pubmed_authors>Zemmoura I</pubmed_authors><pubmed_authors>Ghiringhelli F</pubmed_authors><pubmed_authors>Campone M</pubmed_authors><pubmed_authors>Blechet C</pubmed_authors><pubmed_authors>Diebold MD</pubmed_authors><pubmed_authors>Colin C</pubmed_authors><pubmed_authors>Khallil T</pubmed_authors><pubmed_authors>Loussouarn D</pubmed_authors><pubmed_authors>Bernier M</pubmed_authors><pubmed_authors>Parker F</pubmed_authors><pubmed_authors>Abad M</pubmed_authors><pubmed_authors>Faillot T</pubmed_authors><pubmed_authors>Meyronet D</pubmed_authors><pubmed_authors>Adle-Biassette H</pubmed_authors><pubmed_authors>Labrousse F</pubmed_authors><pubmed_authors>Bourg V</pubmed_authors><pubmed_authors>Carpiuc I</pubmed_authors><pubmed_authors>Gauchotte G</pubmed_authors><pubmed_authors>Colin P</pubmed_authors><pubmed_authors>Ricard D</pubmed_authors><pubmed_authors>Roger P</pubmed_authors><pubmed_authors>Milin S</pubmed_authors><pubmed_authors>Lopez S</pubmed_authors><pubmed_authors>Wager M</pubmed_authors><pubmed_authors>Khettab M</pubmed_authors><pubmed_authors>Touat M</pubmed_authors><pubmed_authors>Motso-Fotso MJ</pubmed_authors><pubmed_authors>Hamdan N</pubmed_authors><pubmed_authors>Djelad A</pubmed_authors><pubmed_authors>Cazals-Hatem D</pubmed_authors><pubmed_authors>Carpentier A</pubmed_authors><pubmed_authors>Vauleon E</pubmed_authors><pubmed_authors>Idbaih A</pubmed_authors><pubmed_authors>Carpentier C</pubmed_authors><pubmed_authors>Ducray F</pubmed_authors><pubmed_authors>Bielle F</pubmed_authors><pubmed_authors>Taillandier L</pubmed_authors><pubmed_authors>Uro-Coste E</pubmed_authors><pubmed_authors>Gueye EM</pubmed_authors><pubmed_authors>Seizeur R</pubmed_authors><pubmed_authors>Chinot O</pubmed_authors><pubmed_authors>Menei P</pubmed_authors><pubmed_authors>Aubriot-Lorton H</pubmed_authors><pubmed_authors>Langlois O</pubmed_authors><pubmed_authors>Figarella-Branger D</pubmed_authors><pubmed_authors>Bronnimann C</pubmed_authors><pubmed_authors>Tabouret E</pubmed_authors><pubmed_authors>Tortel MC</pubmed_authors><pubmed_authors>Maurage CA</pubmed_authors><pubmed_authors>Chotard G</pubmed_authors><pubmed_authors>Godfraind C</pubmed_authors><pubmed_authors>Quintin-Roue I</pubmed_authors><pubmed_authors>Joubert C</pubmed_authors><pubmed_authors>Bauchet L</pubmed_authors><pubmed_authors>Rousselot-Denis C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reappraisal of prognostic factors in CNS WHO grade 3 oligodendrogliomas IDH-mutant and 1p/19q co-deleted: Lessons from the French POLA cohort.</name><description>&lt;h4>Background&lt;/h4>In the POLA cohort, 3 pathological groups of CNS WHO grade 3 oligodendroglioma IDH-mutant and 1p/19q co-deleted have been described: group 1 (high mitotic count only), group 2 (microvascular proliferation MVP and no necrosis), and group 3 (MVP and necrosis).&lt;h4>Methods&lt;/h4>494 patients from the POLA cohort, with a median follow-up of 96 months were included. To identify the impact of the pathological groups and contrast enhancement (CE) in group 1 on overall survival (OS) or progression-free survival (PFS), survival curves were obtained (Kaplan-Meier method) and compared (log-rank test). The prognostic value of clinical factors and CDKN2A homozygous deletion HD were also tested. Multivariate analysis was performed.&lt;h4>Results&lt;/h4>Survival analysis demonstrated that the p</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-04T13:34:52.868Z</modification><creation>2026-05-09T03:12:23.274Z</creation></dates><accession>S-EPMC11889709</accession><cross_references><pubmed>39432559</pubmed><doi>10.1093/neuonc/noae221</doi></cross_references></HashMap>