Diffuse gliomas in patients aged 55 years or over: A suggestion for IDH mutation testing.


Journal

Neuropathology : official journal of the Japanese Society of Neuropathology
ISSN: 1440-1789
Titre abrégé: Neuropathology
Pays: Australia
ID NLM: 9606526

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 24 06 2019
revised: 30 08 2019
accepted: 30 08 2019
pubmed: 24 11 2019
medline: 13 11 2020
entrez: 24 11 2019
Statut: ppublish

Résumé

Diffuse gliomas are defined on the isocitrate dehydrogenase (IDH) gene (IDH) mutational mutational status. The most frequent IDH mutation is IDH1 R132H, which is detectable by immunohistochemistry; other IDH mutations are rare (10%). IDH mutant gliomas have better prognosis. Further, IDH wild-type low-grade (II/III) gliomas have clinical behaviors similar to those of glioblastoma (GBM) and it was suggested that they are submitted to similar post-surgical treatment. The incidence of IDH mutant gliomas (2%) and that of GBMs with non-canonical IDH mutations (< 1%) are very low in patients ≥ 55 years. For this reason, it was suggested that immunohistochemistry against IDH1 R132H is sufficient to classify GBM as IDH wild-type in this age group. However, no indication was provided for IDH mutational testing in low-grade diffuse gliomas. To address this issue, 273 diffuse gliomas were tested for IDH1 R132H immunohistochemistry. 2/4 diffuse astrocytomas (DAs), 4/9 anaplastic astrocytomas (AAs), 2/256 GBMs, and 4/4 oligodendrogliomas had positive staining. No other IDH mutations were found in immuno-negative low-grade cases by DNA sequencing. To validate our findings, we considered 311 diffuse gliomas in patients ≥ 55 years in The Cancer Genome Atlas database. Fifty-five out of 311 gliomas had IDH R132H mutations (9/16 DAs; 8/48 AAs; 3/211 GBMs; 35/36 oligodendrogliomas), one DA, and one oligodendroglioma had other IDH mutations. IDH mutant gliomas had significantly higher frequency of O-6-methylguanine-DNA methyltransferase promoter methylation (P = 0.0008) and longer overall survival (P < 0.0001). In conclusion, low-grade gliomas are a minor part of gliomas (117/584) in patients ≥ 55 years, albeit they represent most IDH mutant gliomas in this age group (64/69 cases). IDH non-canonical mutations can be found in immunonegative low-grade gliomas (2/54). In view of its significance for prognosis and therapeutic management, our results suggest that IDH mutational status is assessed in all diffuse gliomas in patients ≥ 55 years by immunohistochemistry, followed by IDH sequencing in low-grade immunonegative cases.

Identifiants

pubmed: 31758617
doi: 10.1111/neup.12608
doi:

Substances chimiques

Biomarkers, Tumor 0
Isocitrate Dehydrogenase EC 1.1.1.41
IDH1 protein, human EC 1.1.1.42.

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

68-74

Informations de copyright

© 2019 Japanese Society of Neuropathology.

Références

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Auteurs

Valeria Barresi (V)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Albino Eccher (A)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Michele Simbolo (M)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Rekha Cappellini (R)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Giuseppe K Ricciardi (GK)

Pathology and Diagnostics, Section of Neuroradiology, Hospital Trust Verona, Verona, Italy.

Francesca Calabria (F)

Department of Neurology, University of Verona, Verona, Italy.

Marco Cancedda (M)

Neurosciences, Unit of Neurosurgery, Hospital Trust of Verona, Verona, Italy.

Renzo Mazzarotto (R)

Department of Surgery and Oncology, Unit of Radiotherapy, Hospital Trust of Verona, Verona, Italy.

Bruno Bonetti (B)

Department of Neurology, University of Verona, Verona, Italy.

Giampietro Pinna (G)

Neurosciences, Unit of Neurosurgery, Hospital Trust of Verona, Verona, Italy.

Francesco Sala (F)

Neurosciences, Unit of Neurosurgery, Hospital Trust of Verona, Verona, Italy.

Claudio Ghimenton (C)

Department of Pathology and Diagnostics, Section of Pathology, Hospital Trust Verona, Verona, Italy.

Aldo Scarpa (A)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

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