Evidence map›Paper›PMID 42811745›Full record

ArticleBrain pathology (Zurich, Switzerland)2026

Gliomas with pleomorphic and pseudopapillary features (GPAP) are circumscribed tumors with targetable mutations, prolonged survival, and frequent tumor predisposition.

Alberto Picca, Valeria Barresi, Aude Trinquet, Luca Bertero, Lucia Nichelli, Guillaume Chotard, Michèle Bernier, Thomas Gareau, Salah Eddine Oussama Kacimi, Jaydutt Bhalshankar and 26 more

Abstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

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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

36 authors.

Alberto PiccaSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0001-7807-5393
Valeria BarresiNeuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID https://orcid.org/0000-0001-7086-1920
Aude TrinquetService d'Anatomie et Cytologie Pathologiques, CHU de Montpellier, Montpellier, France.ORCID https://orcid.org/0000-0002-8372-8069
Luca BerteroPathology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID https://orcid.org/0000-0001-9887-7668
Lucia NichelliSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0009-0006-0934-5365
Guillaume ChotardService de Pathologie, Groupe Hospitalier Pellegrin, CHU de Bordeaux, Bordeaux, France.ORCID https://orcid.org/0000-0003-0992-1597
Michèle BernierService d'Anatomie et Cytologie Pathologiques, Hôpital Foch, Suresnes, France.
Thomas GareauSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0009-0001-1139-3626
Salah Eddine Oussama KacimiSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0002-7673-9114
Jaydutt BhalshankarSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0001-7184-943X
Mathilde FilserDepartment of Genetics, Institute Curie, Paris, France.
Julien Masliah-PlanchonDepartment of Genetics, Institute Curie, Paris, France.
Marta IolloSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.
Henri MalaizeSorbonne Université, AP-HP, Hôpital Universitaire Pitié-Salpêtrière, Service de Neurochirurgie, Paris, France.
Bertrand MathonSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0002-9182-5846
Luc BauchetInstitut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0003-1077-2496
Kifah KhouriInstitut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, Montpellier, France.
Besma BarkaSorbonne Université, AP-HP, Hôpital Universitaire Pitié-Salpêtriére, Service de Neuropathologie, Paris, France.ORCID https://orcid.org/0009-0007-3651-140X
Hélène MadrySorbonne Université, Unité de Service Production et Analyse des données en Sciences de la vie et en Santé, PASS, Plateforme Post-génomique de la Pitié-Salpêtrière, P3S, Paris, France.ORCID https://orcid.org/0000-0002-8658-4400
Sabrina RossiPathology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-1477-8855
Evelina MieleUniCamillus-Saint Camillus International University of Health Sciences, Rome, Italy.ORCID https://orcid.org/0000-0002-4747-1032
Giuseppe Kenneth RicciardiDepartment of Pathology and Diagnostics, University and Hospital Trust of Verona, Verona, Italy.ORCID https://orcid.org/0000-0001-8536-5794
Catherine CarpentierSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.
Irina CoinService de Neurologie, Hôpital Foch, Suresnes, France.
Marc SansonSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.
Mehdi TouatSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0002-5910-7799
Caroline DehaisSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0003-2910-4930
Alessia PellerinoDivision of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, Turin, Italy.ORCID https://orcid.org/0000-0003-3243-0059
Roberta RudàDivision of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, Turin, Italy.ORCID https://orcid.org/0000-0001-9134-1537
Paola CassoniPathology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID https://orcid.org/0000-0003-1977-7410
Valérie RigauService d'Anatomie et Cytologie Pathologiques, CHU de Montpellier, Montpellier, France.ORCID https://orcid.org/0000-0002-8017-5489
Emmanuelle Uro-CosteService d'Anatomie et Cytologie Pathologiques, CHU de Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-7300-5724
Karima MokhtariSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.
Ahmed IdbaihSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0001-5290-1204
Patrick R BenusiglioDepartment of Medical Genetics, Sorbonne University, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.ORCID https://orcid.org/0000-0003-1003-1997
Franck BielleSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute (ICM), Equipe labellisée Ligue Nationale contre le Cancer, Paris, France.ORCID https://orcid.org/0000-0001-6564-6388

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation profiling of CNS tumors led to the identification of HPAP (high-grade glioma with pleomorphic and pseudopapillary features), a recently proposed entity with variable morphology, recurrent MAP-kinase pathway activating events, and longer survival compared to glioblastoma. We aimed to independently validate and further characterize this entity. We retrieved a multicentric cohort of gliomas compatible with HPAP and performed t-SNE dimensionality reduction on their DNA methylation profile. Clinical, radiological, histological, and molecular data were reviewed. Twenty tumors clustering with previously reported HPAP cases were identified. Median age at diagnosis was 37 years. Radiologically, the tumors appeared as expansive lesions with heterogeneous enhancement and frequent cysts. Histologically, they were well-circumscribed, with papillary and pleomorphic features variably present. Marked histological signs of aggressivity were present in seven. Immunostainings showed expression of GFAP, OLIG2, and CD34. All cases were IDH1/2 wildtype and pMGMT unmethylated. Recurrently mutated genes included TP53, ATRX, RB1, and BRAF. Five patients had germline pathogenic variants in genes associated with hereditary tumor predisposition syndromes (MLH1, BRCA2, CHEK2, NF2, RB1). All patients underwent surgical resection, but subsequent management was heterogeneous. Ten-year estimated survival was 85%. CDKN2A homozygous deletion seemed to identify more aggressive tumors. In conclusion, our data suggest the existence of a novel entity of circumscribed gliomas with long-term survival despite possible high-grade histological presentation, for which we propose the nomenclature "Gliomas with pleomorphic and pseudopapillary features" with a spectrum encompassing provisory grade 2 and 3. A proper identification could guide treatment choices.

Indexed as

BRAFDNA repair pathwaygliomasgliomas with pleomorphic and pseudopapillary featuresmethylome profiling

Identifiers

PMID42811745
PMCPMC13624572

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