Evidence map›Paper›PMID 34967922›Full record

ArticleActa neuropathologica2022

Oligosarcomas, IDH-mutant are distinct and aggressive.

Abigail K Suwala, Marius Felix, Dennis Friedel, Damian Stichel, Daniel Schrimpf, Felix Hinz, Ekkehard Hewer, Leonille Schweizer, Hildegard Dohmen, Ute Pohl and 25 more

Abstract read
In one paragraph

Article in Acta neuropathologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Article
  2. Article
  3. Sarcomatous transformation of an astrocytoma IDH-mutant following radiotherapy.Virchows Archiv : an international journal of pathology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Oligosarcoma with chondroid metaplasia in a French bulldog.The Journal of veterinary medical science · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Glioma.Nature reviews. Disease primers · 2024
    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

35 authors.

Abigail K SuwalaDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Marius FelixDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Dennis FriedelDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Damian StichelDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Daniel SchrimpfDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Felix HinzDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Ekkehard HewerInstitute of Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Leonille SchweizerDepartment of Neuropathology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Hildegard DohmenInstitute of Neuropathology, University of Giessen, Giessen, Germany.
Ute PohlDepartment of Cellular Pathology, Queen Elizabeth Hospital/University Hospitals Birmingham, Birmingham, UK.
Ori StaszewskiInstitute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Andrey KorshunovDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Marco SteinDepartment of Neurosurgery, University Hospital Gießen, Giessen, Germany.
Thidathip WongsurawatFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pornsuk CheunsuacchonFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Sith SathornsumeteeFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Christian KoelscheInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Clinton TurnerCentre for Brain Research, Department of Anatomy and Medical Imaging, Faculty of Medical and Health Sciences, University of Auckland, Auckland, 1023, New Zealand.
Emilie Le RhunDepartment of Neurology and Brain Tumor Center, University Hospital, University of Zurich, Frauenklinikstrasse 26, 8091, Zurich, Switzerland.
Angelika MühlebnerDepartment of Neuro Pathology, Amsterdam UMC, Location AMC, University of Amsterdam, Meibergdreef 9, 1105, Amsterdam, The Netherlands.
Philippe SchuchtDepartment of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010, Bern, Switzerland.
Koray ÖzdumanDepartment of Neurosurgery, Acıbadem University, School of Medicine, Istanbul, Turkey.
Takahiro OnoDepartment of Neurosurgery, Akita University Graduate School of Medicine, Akita, Japan.
Hiroaki ShimizuDepartment of Neurosurgery, Akita University Graduate School of Medicine, Akita, Japan.
Marco PrinzInstitute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Till AckerInstitute of Neuropathology, University of Giessen, Giessen, Germany.
Christel Herold-MendeDepartment of Neurosurgery, University Hospital Heidelberg, Heidelberg, Germany.
Tobias KesslerClinical Cooperation Unit Neurooncology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Wolfgang WickClinical Cooperation Unit Neurooncology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.
David CapperDepartment of Neuropathology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Pieter WesselingLaboratory for Childhood Cancer Pathology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Felix SahmDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Andreas von DeimlingDepartment of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Christian Hartmann *Department of Neuropathology, Institute of Pathology, Hannover Medical School (MHH), Carl-Neuberg-Str. 1, 30625, Hannover, Germany. hartmann.christian@mh-hannover.de.
David E Reuss *Department of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany. david.reuss@med.uni-heidelberg.de.ORCID 0000-0002-4573-6033

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligodendrogliomas are defined at the molecular level by the presence of an IDH mutation and codeletion of chromosomal arms 1p and 19q. In the past, case reports and small studies described gliomas with sarcomatous features arising from oligodendrogliomas, so called oligosarcomas. Here, we report a series of 24 IDH-mutant oligosarcomas from 23 patients forming a distinct methylation class. The tumors were recurrences from prior oligodendrogliomas or developed de novo. Precursor tumors of 12 oligosarcomas were histologically and molecularly indistinguishable from conventional oligodendrogliomas. Oligosarcoma tumor cells were embedded in a dense network of reticulin fibers, frequently showing p53 accumulation, positivity for SMA and CALD1, loss of OLIG2 and gain of H3K27 trimethylation (H3K27me3) as compared to primary lesions. In 5 oligosarcomas no 1p/19q codeletion was detectable, although it was present in the primary lesions. Copy number neutral LOH was determined as underlying mechanism. Oligosarcomas harbored an increased chromosomal copy number variation load with frequent CDKN2A/B deletions. Proteomic profiling demonstrated oligosarcomas to be highly distinct from conventional CNS WHO grade 3 oligodendrogliomas with consistent evidence for a smooth muscle differentiation. Expression of several tumor suppressors was reduced with NF1 being lost frequently. In contrast, oncogenic YAP1 was aberrantly overexpressed in oligosarcomas. Panel sequencing revealed mutations in NF1 and TP53 along with IDH1/2 and TERT promoter mutations. Survival of patients was significantly poorer for oligosarcomas as first recurrence than for grade 3 oligodendrogliomas as first recurrence. These results establish oligosarcomas as a distinct group of IDH-mutant gliomas differing from conventional oligodendrogliomas on the histologic, epigenetic, proteomic, molecular and clinical level. The diagnosis can be based on the combined presence of (a) sarcomatous histology, (b) IDH-mutation and (c) TERT promoter mutation and/or 1p/19q codeletion, or, in unresolved cases, on its characteristic DNA methylation profile.

Indexed as

AdultAgedBrain NeoplasmsFemaleHumansIsocitrate DehydrogenaseMaleMiddle AgedMutationOligodendrogliomaSarcomaIsocitrate Dehydrogenase1p/19qCodeletionDNA methylationGliosarcomaNF1OligodendrogliomaOligosarcomaPrognosisSMASubtypeTERTTP53TypeVariantYAP1

Identifiers

PMID34967922
PMCPMC8742817

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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.