Physician Awareness of the Safe Use of Cyproterone Acetate in Europe: A Survey on the Effectiveness of Additional Risk Minimization Measures.

Autor: Sweeney C; RTI Health Solutions, Research Triangle Park, NC, 27709, USA. csweeney@rti.org., Gilsenan A; RTI Health Solutions, Research Triangle Park, NC, 27709, USA., Calingaert B; RTI Health Solutions, Research Triangle Park, NC, 27709, USA., Moeller C; Bayer AG, Berlin, Germany., Schomakers G; Bayer AG, Berlin, Germany., Sok A; Bayer d.o.o, Sarajevo, Bosnia and Herzegovina., Holzmann R; Bayer AG, Berlin, Germany., Pisa F; Bayer AG, Berlin, Germany.
Jazyk: angličtina
Zdroj: Pharmaceutical medicine [Pharmaceut Med] 2024 Mar; Vol. 38 (2), pp. 145-156. Date of Electronic Publication: 2024 Jan 31.
DOI: 10.1007/s40290-023-00510-x
Abstrakt: Background: Cyproterone acetate (CPA) is a synthetic progesterone derivative introduced in the 1970s and prescribed as antiandrogenic therapy for inoperable prostate cancer, sexual deviations in men, and signs of androgenization in women. In 2020, the CPA summary of product characteristics (SmPC) was revised to include an updated special warning and precaution about (1) the risk of meningioma with increasing cumulative dose and (2) contraindication in patients with meningioma or history of meningioma. A Direct Healthcare Professional Communication (DHPC) was distributed. The European Medicine Agency's Pharmacovigilance Risk Assessment Committee requested that marketing authorization holders in Europe conduct a survey to assess physicians' knowledge of the updated key safety information. The primary objective of this study was to measure physicians' awareness (i.e., did they receive and review the revised SmPC and DHPC) and level of knowledge and understanding of the key safety information pertaining to the restricted use of CPA monotherapy because of the risk of meningioma.
Methods: This cross-sectional web-based survey was administered to dermatologists, endocrinologists, gynecologists, urologists, oncologists, psychiatrists, and general practitioners in France, Germany, Poland, Spain, and the Netherlands who had prescribed CPA monotherapy in the previous 12 months to assess awareness of the risk of meningioma associated with CPA monotherapy.
Results: Of the 613 physicians who participated, 85% correctly indicated that CPA monotherapy should be prescribed with the lowest effective dose, 75% correctly indicated that the risk of meningioma increases with increasing cumulative CPA monotherapy doses, and 73% correctly indicated that treatment with CPA-containing products must be stopped permanently if a patient is diagnosed with meningioma. Overall, 40% of physicians reported having received the DHPC, and 42% reported having received the revised SmPC.
Conclusions: Despite low recall of receipt of the updated SmPC and DHPC, most physicians surveyed are aware of the meningioma risk and actions to mitigate the risk.
(© 2024. Bayer AG.)
Databáze: MEDLINE
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