Off-Label Uses of Ranibizumab and Aflibercept for Age-Related Macular Degeneration in Turkey.

IF 1.2 Q3 OPHTHALMOLOGY
Mevlut Yilmaz, Mehmet Citirik, Hanife Rahmanlar, Ali Alkan, Hakki Gursoz
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引用次数: 0

Abstract

Purpose: To evaluate the clinical and demographic aspects of off-label drug use applications for age-related macular degeneration (AMD) in Turkey.

Methods: Applications for off-label drug use in the treatment of AMD to the Turkish Medicines and Medical Devices Agency (TITCK) in 2018 were retrospectively analyzed. Demographic characteristics, requested drugs, previous treatment regimens, and reasons for applications were evaluated.

Results: The mean age of the patients (n = 209) was 64.9 ± 15.7 years, of which 48.8% were male and 51.2% were female. Ranibizumab (n = 113) comprised 54.1% and aflibercept (n = 96) 45.9% of off-label use applications. No application was made for bevacizumab. The most frequent reasons for application were switchback (49.3%), nonreimbursement of indicated drugs in cases under 50 years of age (24.4%), and failure to complete the loading dose (14.4%).

Conclusions: Ranibizumab was the most requested off-label drug for AMD. There was no application for off-label bevacizumab since its use does not require approval from TITCK. In Turkey, new rules were established for the reimbursement of intravitreal drugs for AMD in 2019. Three doses of intravitreal bevacizumab were required initially for aflibercept and ranibizumab to be covered for reimbursement. There is not enough data in the English literature regarding the off-label use of ranibizumab and aflibercept for AMD. This study provides information about drug regulations and the off-label treatment options preferred by physicians for AMD in Turkey.

雷尼单抗和阿非利塞普在土耳其治疗老年性黄斑变性的超说明书应用
目的:评估土耳其年龄相关性黄斑变性(AMD)的超说明书用药申请的临床和人口统计学方面。方法:回顾性分析2018年向土耳其药品和医疗器械管理局(TITCK)提交的治疗AMD的超说明书用药申请。评估了患者的人口统计学特征、要求的药物、既往治疗方案和申请的原因。结果:209例患者平均年龄64.9±15.7岁,其中男性48.8%,女性51.2%。Ranibizumab (n = 113)和afliberept (n = 96)分别占超说明书用药的54.1%和45.9%。未申请贝伐单抗。最常见的申请原因是切换(49.3%),50岁以下患者的适应症药物未报销(24.4%),以及未能完成加载剂量(14.4%)。结论:雷尼单抗是AMD最需要的说明书外药物。由于贝伐单抗的使用不需要获得tick的批准,因此没有说明书外用药申请。在土耳其,2019年制定了针对AMD的玻璃体内药物报销的新规则。阿非利塞普和雷尼单抗最初需要三剂量的玻璃体内贝伐单抗来报销。在英文文献中,没有足够的数据表明雷尼单抗和阿非利西普在标签外用于AMD。本研究提供了有关药物法规的信息,以及土耳其医生对AMD首选的标签外治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.50
自引率
6.70%
发文量
45
审稿时长
8 weeks
期刊介绍: Peer Review under the responsibility of Iranian Society of Ophthalmology Journal of Current Ophthalmology, the official publication of the Iranian Society of Ophthalmology, is a peer-reviewed, open-access, scientific journal that welcomes high quality original articles related to vision science and all fields of ophthalmology. Journal of Current Ophthalmology is the continuum of Iranian Journal of Ophthalmology published since 1969.
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