Evidence map›Paper›PMID 40887057›Full record

ArticleBrain pathology (Zurich, Switzerland)2026

cIMPACT-NOW update 11: Proposal on adaptation of diagnostic criteria for IDH- and H3-wildtype diffuse high-grade gliomas and for posterior fossa ependymal tumors.

Pieter Wesseling, David Capper, Guido Reifenberger, Chitra Sarkar, Cynthia Hawkins, Arie Perry, Bette Kleinschmidt-DeMasters, Takashi Komori, Werner Paulus, Vani Santosh and 7 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. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. "Updates on diagnostic and prognostic molecular biomarkers of CNS tumors".Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. A brief history of ependymoma.Neuro-oncology · 2026
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

17 authors.

Pieter WesselingDepartment of Pathology, Amsterdam University Medical Centers/VU University Medical Center, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5453-5201
David CapperDepartment of Neuropathology, Charité-Universitätsmedizin Berlin, Corporate Member of Humboldt-Universität and Freie Universität Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0003-1945-497X
Guido ReifenbergerInstitute of Neuropathology, Medical Faculty, Heinrich Heine University and University Hospital Düsseldorf, Düsseldorf, Germany.ORCID https://orcid.org/0000-0002-1419-9837
Chitra SarkarDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.ORCID https://orcid.org/0000-0002-4315-9316
Cynthia HawkinsDepartment of Paediatric Laboratory Medicine, The Hospital for Sick Children, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0003-2618-4402
Arie PerryDepartment of Pathology, UCSF, San Francisco, California, USA.ORCID https://orcid.org/0000-0002-8300-7261
Bette Kleinschmidt-DeMastersDepartment of Pathology, University of Colorado School of Medicine, Aurora, Colorado, USA.
Takashi KomoriDepartment of Laboratory Medicine and Pathology, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6812-2149
Werner PaulusInstitute of Neuropathology, University Hospital Munster, Munster, Germany.
Vani SantoshNational Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0001-8724-2034
Martin van den BentDepartment of Neurology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5710-5127
Michael WellerDepartment of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0002-1748-174X
Stefan M PfisterDivision of Pediatric Neurooncology, German Cancer Research Center, German Cancer Consortium, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-5447-5322
Uri TaboriDepartment of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0002-5019-2683
Dominique Figarella-BrangerService d'Anatomie Pathologique et de Neuropathologie, Hôpital de la Timone, Institut de Neurophysiopathology, Aix-Marseille Univ, APHM, CNRS, Marseille, France.ORCID https://orcid.org/0000-0002-3604-887X
Brent A OrrDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID https://orcid.org/0000-0003-0997-4728
David N LouisDepartment of Pathology, Massachusetts General Hospital, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-9423-4099

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Consortium to Inform Molecular and Practical Approaches to Central Nervous System Tumor Taxonomy (cIMPACT-NOW) updates provide guidelines for the diagnosis of central nervous system (CNS) tumors and suggestions for future World Health Organization (WHO) classification. Following publication of the fifth edition WHO Classification of CNS Tumors (WHO CNS5) in 2021, the cIMPACT-NOW working group "Clarification" reviewed WHO CNS5 and prioritized two topics for further elucidation: (a) distinction of Glioblastoma, IDH-wildtype from Diffuse pediatric-type high-grade glioma, H3-wildtype, and IDH-wildtype and (b) clarification of subgroups of posterior fossa (PF) ependymal tumors. Recommendations regarding the IDH- and H3-wildtype diffuse high-grade gliomas include: (1) use caution assigning CNS WHO grade 4 (diagnosis of Glioblastoma, IDH-wildtype) to a "TERT promoter only", histologically low-grade, IDH-wildtype tumor; (2) EGFR gene amplification and +7/-10 chromosome copy number alterations should not be used as solitary defining features for diagnosing high-grade gliomas as Glioblastoma, IDH-wildtype in patients <40 years of age; (3) Diffuse pediatric-type high-grade glioma, H3-wildtype, and IDH-wildtype should be considered in the differential diagnosis in adults, especially those <40 years of age; (4) PDGFRA alteration, EGFR alteration, or MYCN amplification count as key molecular features of Diffuse pediatric-type high-grade glioma, H3-wildtype, and IDH-wildtype only in patients <25 years. Guidelines for improved diagnosis of posterior fossa ependymal tumors include: (1) immunohistochemical demonstration of nuclear EZHIP supports classification as PF group A ependymoma; (2) a PF ependymoma with retained nuclear H3 K27me3 expression and no nuclear EZHIP overexpression for which DNA methylation profiling is not performed should be considered as PF ependymoma, "not otherwise specified"; (3) for emerging tumors not included in WHO CNS5, "not elsewhere classified" (NEC) can be added to the diagnosis. Of note, these recommendations are not formal changes to the WHO definitions and diagnostic criteria but are intended to provide diagnostic guidance in advance of WHO CNS6.

Indexed as

Brain NeoplasmsCentral Nervous System NeoplasmsEpendymomaGliomaInfratentorial NeoplasmsHistonesHumansIsocitrate DehydrogenaseNeoplasm GradingWorld Health OrganizationHistonesIsocitrate DehydrogenasecIMPACT‐NOWclarificationdiffuse pediatric‐type high‐grade gliomaGlioblastoma, IDH‐wildtypeposterior fossa ependymomaWHO classification

Identifiers

PMID40887057
PMCPMC12695693

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.