Functional and Anatomic Outcomes at 12 Months After Switching to Faricimab in Treatment-Recalcitrant Neovascular Age-Related Macular Degeneration.

IF 1.3 Q4 OPHTHALMOLOGY
S Saeed Mohammadi, Hayden Sikora, Jay Bisen, Helena Kim, Michael Drakopoulos, Arnold Nadel, Nikoo Hamzeh, Harnaina Bains, Alice T Lyon, Rukhsana G Mirza
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Abstract

Purpose: To evaluate functional and anatomic outcomes over 12 months in patients with recalcitrant neovascular age-related macular degeneration (nAMD) whose treatment was transitioned to faricimab. Methods: This retrospective observational study included 36 patients (41 eyes) with treatment-recalcitrant nAMD previously treated with bevacizumab, ranibizumab, or aflibercept. Patients received 4 monthly intravitreal faricimab injections followed by individualized treatment intervals. Best-corrected visual acuity (BCVA), optical coherence tomography (OCT) images, and swept-source OCT angiography images were assessed at baseline, 6 months, and 12 months. Anatomic features evaluated included intraretinal fluid (IRF), subretinal fluid (SRF), pigment epithelial detachment (PED), macular neovascularization (MNV), and geographic atrophy (GA). Results: Mean (±SD) BCVA remained stable over the 12-month period (baseline, 0.289 ± 0.350 logMAR; 12 months, 0.306 ± 0.394 logMAR; P = .41). Treatment intervals increased from a mean of 5.29 weeks prior to the switch to faricimab to 7.58 weeks afterward. Anatomically, the proportion of eyes without IRF or SRF improved from 34.14% at baseline to 74.68% at 12 months. A significant reduction in PED maximum height was observed at 6 months, along with decreases in mean PED height and volume. MNV metrics demonstrated a significant decline in vessel area density at 6 months (P = .031), although no sustained significant changes were observed at 12 months. GA size increased by a mean of 0.41 mm²/year over the study period (P = .026). Conclusions: Switching to faricimab in treatment-recalcitrant nAMD maintained visual acuity, improved anatomic outcomes, and significantly extended injection intervals. These findings underscore faricimab's efficacy in managing refractory nAMD cases.

法瑞昔单抗治疗难治性新生血管性年龄相关性黄斑变性12个月后的功能和解剖结果
目的:评估顽固性新生血管性年龄相关性黄斑变性(nAMD)患者12个月以上的功能和解剖结果,这些患者的治疗过渡到faricimab。方法:这项回顾性观察研究纳入了36例(41只眼)治疗难治性nAMD患者,这些患者之前曾接受过贝伐单抗、雷尼单抗或阿非利塞普治疗。患者接受4个月玻璃体内法利西单抗注射,然后进行个体化治疗间隔。在基线、6个月和12个月时评估最佳矫正视力(BCVA)、光学相干断层扫描(OCT)图像和扫描源OCT血管造影图像。解剖特征评估包括视网膜内液(IRF)、视网膜下液(SRF)、色素上皮脱离(PED)、黄斑新生血管(MNV)和地理萎缩(GA)。结果:平均(±SD) BCVA在12个月期间保持稳定(基线,0.289±0.350 logMAR; 12个月,0.306±0.394 logMAR; P = 0.41)。治疗间隔从改用法昔单抗前的平均5.29周增加到改用法昔单抗后的平均7.58周。解剖上,无IRF或SRF的眼睛比例从基线时的34.14%提高到12个月时的74.68%。在6个月时观察到PED最大高度显著降低,同时平均PED高度和体积也下降。MNV指标显示在6个月时血管面积密度显著下降(P = 0.031),尽管在12个月时没有观察到持续的显著变化。在研究期间,GA尺寸平均增加了0.41 mm²/年(P = 0.026)。结论:改用法昔单抗治疗难治性nAMD可维持视力,改善解剖结果,并显著延长注射间隔。这些发现强调了faricimab在治疗难治性nAMD病例中的有效性。
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
1.20
自引率
16.70%
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