Evidence map›Paper›PMID 40159303›Full record

ArticleCancer2025

Characteristics, outcome, and prognostic factors of young patients with central nervous system World Health Organization grade 3 oligodendrogliomas IDH-mutant and 1p/19q codeleted: A French POLA network study.

Alexandre Bertucci, Ondine Dufour, Romain Appay, Vincent Harlay, François Ducray, Charlotte Bronnimann, Apolline Djelad, Elisabeth Cohen-Jonathan Moyal, Mario Campone, Olivier Langlois and 13 more

Abstract read
In one paragraph

Article in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Alexandre BertucciAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, GlioME Team, Marseille, France.ORCID https://orcid.org/0000-0002-9267-1770
Ondine DufourAPHM, CHU Timone, Service de Neurooncologie, Marseille, France.
Romain AppayAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, GlioME Team, Marseille, France.
Vincent HarlayAPHM, CHU Timone, Service de Neurooncologie, Marseille, France.
François DucrayHospices Civils de Lyon, Hôpital Neurologique, Neuro-oncology Department, Department of Cancer Cell Plasticity, Cancer Research Center of Lyon, Claude Bernard University, Lyon, France.
Charlotte BronnimannMedical Oncology Department, CHU de Bordeaux, Bordeaux, France.
Apolline DjeladNeurosurgery Department, CHU de Lille, Lille, France.
Elisabeth Cohen-Jonathan MoyalRadiotherapy Department, IUCT-Oncopôle, Toulouse, France.
Mario CamponeMedical Oncology Department, Centre René Gauducheau, Saint-Herblain, France.
Olivier LangloisNeurosurgery Department, CHU Charles Nicolle, Rouen, France.
Mathilde DucloieNeurology Department, CHU Caen, Caen, France.
Elodie VauleonCentre Eugène Marquis, Medical Oncology, INSERM, University of Rennes, Rennes, France.
Nadia YounanNeurology Department, Hôpital Foch, Suresnes, France.
Christine DesenclosNeurosurgery Department, Hôpital Nord, CHU Amiens, Amiens, France.
Carole RamirezNeurology Department, Hôpital Nord, CHU Saint-Étienne, Saint-Priest en Jarez, France.
Mehdi TouatSorbonne Université, Inserm, CNRS, UMR S 1127, Institut du Cerveau, ICM, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Service de Neuro-oncologie, Paris, France.
Ahmed IdbaihSorbonne Université, Inserm, CNRS, UMR S 1127, Institut du Cerveau, ICM, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Service de Neuro-oncologie, Paris, France.
Céline BequetAPHM, CHU Timone, Service de Neurooncologie, Marseille, France.
Dominique Figarella-BrangerAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, GlioME Team, Marseille, France.
Caroline DehaisSorbonne Université, Inserm, CNRS, UMR S 1127, Institut du Cerveau, ICM, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Service de Neuro-oncologie, Paris, France.
Olivier ChinotAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, GlioME Team, Marseille, France.
Emeline TabouretAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, GlioME Team, Marseille, France.
POLA network

Funding

French Institut National du Cancer
6 · The paper itself

Abstract

backgroundBrain tumors represent one of the main causes of cancer-related mortality in young patients. Among them, oligodendrogliomas (OG) are adult-type diffuse gliomas with the best prognosis. Nevertheless, characterization of these tumors in the young population remains poorly documented. Our objective was to characterize the population of young adults under 40 years of age with grade 3 OG in the POLA cohort.

methodsClinical data prospectively collected for all patients registered with grade 3 OG between April 2009 and August 2021 were extracted from the national POLA database. This study compared the patient subgroup <40 years of age to the one >40 years of age.

resultsThe authors included 111 patients <40 years old and 363 patients ≥40 years old. Treatment received did not differ significantly between the two subgroups. Temporal location was more frequent in older patients (p = .009). Patients <40 years old presented more often seizure as initial symptom (p = .003). They had less frequent chromosome 9p loss (p < .001) and less CDKN2A homozygous deletion (p = .024). Median progression-free survival (PFS) was 123 months (range, 86-not reached [NR]) versus 88 months (range, 67-117) (p = .082) and median overall survival (OS) was not reached (range, 147-NR) versus 163 months (range, 137-NR) (p < .001) in younger and older subgroups, respectively. In multivariate analysis, complete or subtotal resection (p = .014) and seizure at diagnosis (p = .032) were associated with better OS.

conclusionYoung patients with grade 3 OG have distinct clinical presentation, molecular features, and outcomes compared to the older patients.

Indexed as

Brain NeoplasmsIsocitrate DehydrogenaseOligodendrogliomaAdolescentAdultAge FactorsChromosome DeletionChromosomes, Human, Pair 1Chromosomes, Human, Pair 19FemaleFranceHumansMaleMiddle AgedMutationNeoplasm GradingIDH1 protein, humanIsocitrate Dehydrogenasegliomagrade 3 oligodendrogliomamolecular featuresprognostic factorsyoung patient

Identifiers

PMID40159303
PMCPMC11955080

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.