Prognostic Value of Histopathological Features and Loss of H3K27me3 Immunolabeling in Anaplastic Meningioma: A Multicenter Retrospective Study

Author:

Gauchotte Guillaume123,Peyre Matthieu456,Pouget Celso12,Cazals-Hatem Dominique7,Polivka Marc,Rech Fabien89,Varlet Pascale10,Loiseau Hugues1112,Lacomme Stéphanie3,Mokhtari Karima413,Kalamarides Michel45,Bielle Franck41314

Affiliation:

1. INSERM U1256, Faculty of Medicine, Université de Lorraine, Vandoeuvre-lès-Nancy

2. Department of Pathology, CHRU, Nancy, France

3. Centre de Ressources Biologiques, BB-0033-00035 (GG, SL), CHRU, Nancy, France

4. Sorbonne Universités, INSERM, CNRS, UMR S 1127, Institut du Cerveau et de la Moelle Épinière, Paris, France

5. Department of Neurosurgery, Groupe Hospitalier Pitié Salpêtrière, AP-HP (MP, MK), Paris, France

6. Department of Pathology, Hôpital Lariboisière, AP-HP, Paris, France

7. Department of Pathology, Hôpital Beaujon, AP-HP, Clichy, France

8. Department of Neurosurgery, CHRU, Nancy, France

9. Institut des Neurosciences, INSERM U1051, Montpellier, France

10. Department of Neuropathology, Centre Hospitalier Saint-Anne, Paris, France

11. Department of Neurosurgery, CEREPEG, Hôpital Pellegrin Tripode, Bordeaux, France

12. EA 7435 – IMOTION University of Bordeaux (HL), Bordeaux

13. AP-HP, Department of Neuropathology, Hôpital de la Pitié Salpêtrière, Paris, France

14. SiRIC CURAMUS (Cancer United Research Associating Medicine, University & Society), Site de Recherche Intégrée sur le Cancer IUC, APHP.6, Sorbonne Université (FB), Paris, France

Abstract

Abstract The diagnosis of anaplastic meningioma (AM) (WHO grade III) is based on the presence of a high mitotic index (MI) and/or overt anaplasia. Only few data exist about the reproducibility and prognostic value of overt anaplasia. Additionally, the prognostic value of H3K27me3 loss in AM has not yet been demonstrated. Our objectives were to evaluate the reproducibility and prognostic value of WHO criteria and H3K27me3 loss in a multicenter series of 66 AM. Interobserver reproducibility was good for the determination of WHO grade (Kappa = 0.671) and MI (intraclass correlation coefficient [ICC] = 0.649), and fair for assessment of overt anaplasia (Kappa = 0.366). Patients with meningiomas showing high MI had significantly shorter overall survival (OS) than patients with meningiomas showing overt anaplasia without high MI (p = 0.009). OS was significantly lower in case of overt anaplasia with low MI (<20/1.6 mm2) than in atypical meningiomas (p = 0.008). H3K27me3 loss was present in 10/47 (21%) of AM and independently associated with shorter OS (p = 0.036; Cox multivariate analysis), with a good reproducibility (Kappa = 0.643). In conclusion, the presence of overt anaplasia could give additional prognostic information in tumors lacking high MI. Finally, loss of H3K27me3 is an easy-to-use and reproducible marker of poorer prognosis.

Funder

French National Cancer Institute

French Ministry of Solidarity and Health and INSERM

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Neurology,General Medicine,Pathology and Forensic Medicine

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