Meningiomas and cyproterone acetate: a retrospective, monocentric cohort of 388 patients treated by surgery or radiotherapy for intracranial meningioma.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 14 11 2020
accepted: 16 12 2020
revised: 15 12 2020
pubmed: 5 1 2021
medline: 3 11 2021
entrez: 4 1 2021
Statut: ppublish

Résumé

Meningiomas are the most common intracranial tumors, accounting for 20-30% of central nervous system tumors. Recently, the European Medicines Agency issued an alert on cyproterone acetate (CPA) based on the results of a study that found an increased risk of meningioma 7 to 20 times higher when a patient is on CPA. The primary objective of this study was to determine the prevalence of CPA exposure in patients who had one or more intracranial meningiomas treated surgically or with radiation therapy. The secondary objectives were to establish a description of the patients who had intracranial meningioma in Nantes and to establish whether there was a difference in the intrinsic and tumoral characteristics of patients exposed to CPA compared with patients who had no hormonal exposure and patients who had been exposed to other hormones. Monocentric, retrospective study including all patients treated by surgery or radiotherapy for intracranial meningioma from 2014 to 2017 excluding those with a history of exposure to ionizing radiation or neurofibromatosis type 2. 388 patients were included, 277 were treated by surgery and 111 by radiotherapy. 3.9% of the patients had a history or current use of CPA, 16.2% were taking other hormonal treatment. Compared with the group without hormonal exposure, the CPA-exposed group had significantly an earlier onset of meningiomas at 48.9 vs. 61.9 years (p = 0.0005) and had more multiple meningiomas, 26.7% vs. 6.1% (p = 0.0115). In our study, patients with a history or current use of CPA had significantly more meningiomas and were significantly younger at the onset.

Identifiants

pubmed: 33392938
doi: 10.1007/s11060-020-03683-6
pii: 10.1007/s11060-020-03683-6
doi:

Substances chimiques

Androgen Antagonists 0
Cyproterone Acetate 4KM2BN5JHF

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115-123

Références

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Auteurs

Edouard Samarut (E)

Neurotraumatology, Neurosurgery Department, Hotel-Dieu, CHU Nantes, Nantes, France.

Alexandre Lugat (A)

L'institut du thorax, Endocrinology, Diabetology and Nutrition Department, CHU Nantes, Nantes, France.
Inserm UMR 1232, CRCINA, Université d'Angers, Université de Nantes, Nantes, France.

Aymeric Amelot (A)

Neurosurgery Department, Bretonneau Hospital, CHRU Tours, Tours, France.
Inserm UMR 1253, Université de Tours, Tours, France.

Emeric Scharbarg (E)

L'institut du thorax, Endocrinology, Diabetology and Nutrition Department, CHU Nantes, Nantes, France.

Samy Hadjadj (S)

L'institut du thorax, Endocrinology, Diabetology and Nutrition Department, CHU Nantes, Nantes, France.

Claire Primot (C)

Inserm UMR 1413, CIC, Endocrinology, Diabetology and Nutrition, CHU Nantes, Nantes, France.

Delphine Loussouarn (D)

Pathology Department, Hotel-Dieu, CHU Nantes, Nantes, France.

François Thillays (F)

Radiotherapy Department, Institut de Cancérologie de l'Ouest (ICO), Saint-Herblain, France.

Kevin Buffenoir (K)

Neurotraumatology, Neurosurgery Department, Hotel-Dieu, CHU Nantes, Nantes, France.

Bertrand Cariou (B)

L'institut du thorax, Endocrinology, Diabetology and Nutrition Department, CHU Nantes, Nantes, France.

Delphine Drui (D)

L'institut du thorax, Endocrinology, Diabetology and Nutrition Department, CHU Nantes, Nantes, France. delphine.drui@chu-nantes.fr.

Vincent Roualdes (V)

Neurotraumatology, Neurosurgery Department, Hotel-Dieu, CHU Nantes, Nantes, France. vincent.roualdes@chu-nantes.fr.

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