Igwe Franklin, Lodha Amit, Ravindran Arun
Novartis Pharma A.G., Basel, Switzerland.
Novartis Pharmaceuticals Corp., East Hanover, USA.
Ophthalmol Ther. 2023 Feb;12(1):593-598. doi: 10.1007/s40123-022-00617-5. Epub 2022 Dec 5.
Brolucizumab, a low-molecular weight anti-vascular endothelial growth factor, was approved in the USA in October 2019 for the treatment of neovascular age-related macular degeneration. Following post-marketing reports of vasculitis, including retinal occlusive vasculitis, a safety signal of retinal vasculitis (RV) and/or retinal vascular occlusion (RO) that may result in severe vision loss was confirmed. This brief communication reviews the trends in the cumulative reporting rates of RV and/or RO and associated vision loss from May 2020 to September 2022.
This is a descriptive analysis of the cumulative post-marketing reporting rates of RV and/or RO cases, and associated vision loss included in the Novartis safety database between May 2020 and September 2022, utilizing an enhanced pharmacovigilance program.
The RV-alone rates demonstrated an upward trend, rising to 5.1 events per 10,000 injections by October 2020 and subsequently remained stable until July 2021. Thereafter, the rate for RV-alone events increased modestly until October 2021 and then remained stable until September 2022. The RO-alone rates increased to 3.4 events per 10,000 injections by January 2021 and subsequently remained stable until September 2022. The combined reports of RV and RO showed an upward trend until December 2020 (7.5 events per 10,000 injections), followed by a plateau until September 2021 and then a downward trend until September 2022. Vision loss associated with RV and/or RO progressively increased until December 2020 (5.9 events per 10,000 injections) followed by a declining trend until September 2022 to the most recent reporting rate of 4.1 events per 10,000 injections.
The cumulative post-marketing reporting rates of vision loss associated with RV and/or RO, following brolucizumab treatment, have shown a declining trend after an initial rise in the reporting rates immediately after identification of the safety signal.
布罗利尤单抗是一种低分子量抗血管内皮生长因子药物,于2019年10月在美国获批用于治疗新生血管性年龄相关性黄斑变性。在包括视网膜闭塞性血管炎在内的血管炎上市后报告出现后,一种可能导致严重视力丧失的视网膜血管炎(RV)和/或视网膜血管阻塞(RO)的安全信号得到确认。本简短通讯回顾了2020年5月至2022年9月期间RV和/或RO的累积报告率趋势以及相关的视力丧失情况。
这是一项对2020年5月至2022年9月期间诺华安全数据库中包含的RV和/或RO病例的累积上市后报告率以及相关视力丧失情况的描述性分析,采用了强化药物警戒计划。
单纯RV发生率呈上升趋势,到2020年10月升至每10000次注射5.1例事件,随后在2021年7月前保持稳定。此后,单纯RV事件发生率在2021年10月前略有上升,然后在2022年9月前保持稳定。单纯RO发生率到2021年1月升至每10000次注射3.4例事件,随后在2022年9月前保持稳定。RV和RO的联合报告在2020年12月前呈上升趋势(每10000次注射7.5例事件),随后在2021年9月前保持平稳,然后在2022年9月前呈下降趋势。与RV和/或RO相关的视力丧失在2020年12月前逐渐增加(每10000次注射5.9例事件),随后呈下降趋势,到2022年9月降至最近报告率每10000次注射4.1例事件。
在识别出安全信号后,布罗利尤单抗治疗后与RV和/或RO相关的视力丧失的累积上市后报告率在最初上升后呈下降趋势。