Three-month outcomes of treatment with faricimab or aflibercept for neovascular age-related macular degeneration: a propensity score matching study in a Japanese population.

IF 2.4 3区 医学 Q2 OPHTHALMOLOGY Graefe’s Archive for Clinical and Experimental Ophthalmology Pub Date : 2024-12-01 Epub Date: 2024-07-29 DOI:10.1007/s00417-024-06582-y
Yosuke Fukuda, Shoji Notomi, Satomi Shiose, Yusuke Maehara, Kohei Kiyohara, Kohta Fujiwara, Sawako Hashimoto, Kumiko Kano, Keijiro Ishikawa, Toshio Hisatomi, Koh-Hei Sonoda
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Abstract

Purpose: This study aimed to compare the treatment outcomes of patients with neovascular age-related macular degeneration (nAMD) who initially received faricimab or aflibercept treatment using propensity score matching (PSM) to align patient backgrounds.

Methods: Patients with treatment-naïve nAMD who received either faricimab or aflibercept for three consecutive monthly injections as the loading phase were enrolled in this study. In the 1:1 PSM, sex, age, best-corrected visual acuity (BCVA), central macular thickness (CMT), central choroidal thickness (CCT), and AMD subtypes in the pre-treatment state were selected as covariates. We examined the BCVA, CMT, CCT, and remaining fluid at 1-, 2-, and 3-month after the first injection.

Results: After PSM, 43 eyes were included in the faricimab and aflibercept group each. Both groups showed significant improvements in BCVA, CMT, and CCT at 1-, 2-, and 3-month after the initial injection compared with baseline. Meanwhile, no significant differences were observed between the two groups at any time point regarding BCVA, CMT, and CCT. At 1-month, 18.6% of patients in the faricimab group and 41.9% in the aflibercept group demonstrated residual subretinal fluid or intraretinal fluid, with a significant difference between the groups (P = 0.03).

Conclusion: The BCVA improved after three loading injections of both faricimab and aflibercept. Faricimab may provide a favorable early treatment response in reducing subretinal fluid in a Japanese cohort.

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法尼单抗或阿弗利百普治疗新生血管性老年性黄斑变性的三个月疗效:一项针对日本人群的倾向得分匹配研究。
目的:本研究旨在比较最初接受法尼单抗或阿弗利百普治疗的新生血管性年龄相关性黄斑变性(nAMD)患者的治疗效果:本研究招募了未经治疗的nAMD患者,他们在负荷阶段每月连续注射三次法利单抗或阿弗利百普。在1:1 PSM中,性别、年龄、最佳矫正视力(BCVA)、黄斑中心厚度(CMT)、脉络膜中心厚度(CCT)和治疗前的AMD亚型被选作协变量。我们检查了首次注射后 1 个月、2 个月和 3 个月的 BCVA、CMT、CCT 和剩余液体:PSM后,法尼单抗组和阿夫利拜单抗组各有43只眼睛。与基线相比,两组在首次注射后 1、2 和 3 个月的 BCVA、CMT 和 CCT 均有明显改善。同时,两组在任何时间点的 BCVA、CMT 和 CCT 均无明显差异。1个月时,18.6%的法尼单抗组患者和41.9%的阿弗利百普组患者出现残留视网膜下积液或视网膜内积液,组间差异显著(P = 0.03):结论:法利单抗和阿弗利百普注射三次后,BCVA均有所改善。结论:法利单抗和阿夫利百普注射三次后,BCVA均有所改善。法利单抗在减少视网膜下积液方面可为日本患者提供良好的早期治疗效果。
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来源期刊
CiteScore
5.40
自引率
7.40%
发文量
398
审稿时长
3 months
期刊介绍: Graefe''s Archive for Clinical and Experimental Ophthalmology is a distinguished international journal that presents original clinical reports and clini-cally relevant experimental studies. Founded in 1854 by Albrecht von Graefe to serve as a source of useful clinical information and a stimulus for discussion, the journal has published articles by leading ophthalmologists and vision research scientists for more than a century. With peer review by an international Editorial Board and prompt English-language publication, Graefe''s Archive provides rapid dissemination of clinical and clinically related experimental information.
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