Evidence map›Paper›PMID 36571817›Full record

ArticleNeuro-oncology2023

Mitotic count is prognostic in IDH mutant astrocytoma without homozygous deletion of CDKN2A/B. Results of consensus panel review of EORTC trial 26053 (CATNON) and EORTC trial 22033-26033.

Johan M Kros, Elisabeth Rushing, Aimé L Uwimana, Aurelio Hernández-Laín, Alex Michotte, Maysa Al-Hussaini, Franck Bielle, Christian Mawrin, Gianluca Marucci, C Mircea S Tesileanu and 5 more

Abstract readConsensus Statement
In one paragraph

Article in Neuro-oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Sarcomatous transformation of an astrocytoma IDH-mutant following radiotherapy.Virchows Archiv : an international journal of pathology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. IDH mutant high-grade gliomas.Frontiers in molecular neuroscience · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. Glioma.Nature reviews. Disease primers · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Prognostic implication ofNeuro-oncology advances
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Johan M KrosDepartment of Pathology, Laboratory for Tumor Immunopathology, Erasmus Medical Center, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Elisabeth RushingDepartment of Neuropathology, University Hospital Zurich, University of Zurich, Switzerland.
Aimé L UwimanaEuropean Organization for Research and Treatment of Cancer Headquarters, Brussels, Belgium.
Aurelio Hernández-LaínDepartment of Pathology (Neuropathology), Hospital Universitario 12 de Octubre Research Institute, Madrid, Spain.
Alex MichotteMedische Oncologie, Oncologisch Centrum, Academisch Ziekenhuis Vrije Universiteit Brussel (AZ-VUB), Brussel, Belgium.
Maysa Al-HussainiDepartment of Pathology and Laboratory Medicine, King Hussein Cancer Centre, Amman, Jordan.
Franck BielleSorbonne Université, AP-HP, Institut du Cerveau, Paris Brain Institute, ICM, Inserm, CNRS, Hôpitaux Universitaires La Pitié Salpêtrière, Charles Foix, Service de Neuropathologie, Paris, France.ORCID 0000-0001-6564-6388
Christian MawrinDepartment of Neuropathology, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Gianluca MarucciNeuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
C Mircea S TesileanuDepartment of Neurology, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Roger StuppNorthwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Brigitta BaumertDepartment of Radiation Oncology, MediClin Robert Janker Clinic and Clinical Cooperation Unit Neurooncology, University of Bonn Medical Centre, Bonn, Germany.
Martin van den BentNeurooncology Unit, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Pim J FrenchNeurooncology Unit, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0002-0668-9529
Thierry GorliaEuropean Organization for Research and Treatment of Cancer Headquarters, Brussels, Belgium.

Funding

Cancer Research UK 7267Medical Research Council MC_UU_12023/10
6 · The paper itself

Abstract

backgroundGliomas with IDH1/2 mutations without 1p19q codeletion have been identified as the distinct diagnostic entity of IDH mutant astrocytoma (IDHmut astrocytoma). Homozygous deletion of Cyclin-dependent kinase 4 inhibitor A/B (CDKN2A/B) has recently been incorporated in the grading of these tumors. The question of whether histologic parameters still contribute to prognostic information on top of the molecular classification, remains unanswered. Here we evaluated consensus histologic parameters for providing additional prognostic value in IDHmut astrocytomas.

methodsAn international panel of seven neuropathologists scored 13 well-defined histologic features in virtual microscopy images of 192 IDHmut astrocytomas from EORTC trial 22033-26033 (low-grade gliomas) and 263 from EORTC 26053 (CATNON) (1p19q non-codeleted anaplastic glioma). For 192 gliomas the CDKN2A/B status was known. Consensus (agreement ≥ 4/7 panelists) histologic features were tested together with homozygous deletion (HD) of CDKN2A/B for independent prognostic power.

resultsAmong consensus histologic parameters, the mitotic count (cut-off of 2 mitoses per 10 high power fields standardized to a field diameter of 0.55 mm and an area of 0.24 mm2) significantly influences PFS (P = .0098) and marginally the OS (P = .07). Mitotic count also significantly affects the PFS of tumors with HD CDKN2A/B, but not the OS, possibly due to limited follow-up data.

conclusionThe mitotic index (cut-off 2 per 10 40× HPF) is of prognostic significance in IDHmut astrocytomas without HD CDKN2A/B. Therefore, the mitotic index may direct the therapeutic approach for patients with IDHmut astrocytomas with native CDKN2A/B status.

Indexed as

AstrocytomaBrain NeoplasmsGliomaCyclin-Dependent Kinase Inhibitor p16HomozygoteHumansIsocitrate DehydrogenaseMutationPrognosisSequence DeletionCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16Isocitrate DehydrogenaseastrocytomaCDKN2A/BgliomagradingIDH mutationmolecular pathologyprognosisproliferation

Identifiers

PMID36571817
PMCPMC10398806

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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.