法利西单抗对阿非利赛普低反应者的额外影响:两种抗vegf药物切换后新生血管年龄相关性黄斑变性患者的视网膜形态和功能

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-09-03 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S530355
Jan Rothbächer, Haidar Khalil, Markus Eidherr, Matthias Bolz
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引用次数: 0

摘要

目的:评估在现实生活中,新生血管性年龄相关性黄斑变性(nAMD)患者从阿非利赛普过渡到法利昔单抗玻璃体内治疗对视网膜结构和功能方面的影响。患者和方法:对奥地利林茨开普勒大学医院眼视光学部49例(57只眼)nAMD患者进行回顾性临床研究。之前每月接受Aflibercept注射但治疗效果不理想的患者,在2022年12月至2023年12月期间切换到玻璃体内Faricimab并随访。结果:第5次注射Faricimab前的平均治疗间隔为5.35±1.49周,明显长于Aflibercept的月间隔(p < 0.001)。平均基线视网膜中央厚度(CRT)为267.82±76.00µm,在第1个月已显著下降至249.61±65.35µm (p < 0.001)。第四次玻璃体内注射后,CRT为252.95±56.96µm,无明显变化(p = 0.134)。出现视网膜下积液(SRF)和视网膜内积液(IRF)的患者数量显著减少。在纤维血管色素上皮脱离(PED)的眼睛中,超过一半的病例不可能延长间隔。对于浆液性和类鼻窦炎性PED以及高反射灶(HRF)的眼睛,大多数在转换后表现出显著的反应。结论:初始负荷剂量可能有利于延长法利西单抗的额外作用,以减少患有nAMD和先前对阿非利西普低反应的眼睛的视网膜肿胀。浆液性和类德鲁桑性儿科患儿似乎比纤维血管性儿科患儿受益更多。在PED患者中,高剂量的肠内HRF是Faricimab反应良好的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Additional Effects of Faricimab in Aflibercept Low-Responders: Retinal Morphology and Function in Eyes with Neovascular Age Related Macular Degeneration Following a Switch Between Two Anti-VEGF Agents.

Additional Effects of Faricimab in Aflibercept Low-Responders: Retinal Morphology and Function in Eyes with Neovascular Age Related Macular Degeneration Following a Switch Between Two Anti-VEGF Agents.

Additional Effects of Faricimab in Aflibercept Low-Responders: Retinal Morphology and Function in Eyes with Neovascular Age Related Macular Degeneration Following a Switch Between Two Anti-VEGF Agents.

Additional Effects of Faricimab in Aflibercept Low-Responders: Retinal Morphology and Function in Eyes with Neovascular Age Related Macular Degeneration Following a Switch Between Two Anti-VEGF Agents.

Purpose: To assess how transitioning from an Aflibercept to a Faricimab intravitreal treatment impacts retinal structures and functional aspects in patients with neovascular age related macular degeneration (nAMD) in a real-life setting.

Patients and methods: A retrospective clinical study including 49 patients (57 eyes) with nAMD at the Department of Ophthalmology and Optometry, Kepler University Hospital, Linz, Austria was performed. The patients, who had previously been receiving monthly Aflibercept injections with an unsatisfactory treatment response, were switched to intravitreal Faricimab and followed-up between 12/2022 and 12/2023.

Results: The mean treatment-interval before the fifth injection with Faricimab was 5.35 ± 1.49 weeks and was therefore significantly longer compared to the monthly interval with Aflibercept (p < 0.001). Mean baseline central retinal thickness (CRT) was 267.82 ± 76.00 µm and decreased significantly already at month 1 to 249.61 ± 65.35 µm (p < 0.001). After the fourth intravitreal injection, there was no significant change with a CRT of 252.95 ± 56.96 µm (p = 0.134). There was a significant reduction in the number of patients showing subretinal fluid (SRF) and intraretinal fluid (IRF). In eyes with fibrovascular pigment epithelium detachment (PED), an interval extension was not possible in more than half of the cases. Eyes with serous and drusenoid PED and a rather high amount of hyper-reflective foci (HRF), the majority showed a significant response after the switch.

Conclusion: An initial loading dose could be beneficial to elongate Faricimab's additional effect of reducing retinal swelling in eyes with nAMD and previous low-response to Aflibercept. Serous and drusenoid PEDs seem to benefit more than fibrovascular PEDs. A high amount of intraretinal HRF in patients with PED was a sign for good respondence to Faricimab.

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