Fukuda Yosuke, Notomi Shoji, Shiose Satomi, Maehara Yusuke, Kiyohara Kohei, Fujiwara Kohta, Hashimoto Sawako, Kano Kumiko, Ishikawa Keijiro, Hisatomi Toshio, Sonoda Koh-Hei
Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Department of Ophthalmology, Fukuoka University Chikushi Hospital, 1-1-1 Zokumyouin, Chikushino, 818-8502, Fukuoka, Japan.
Graefes Arch Clin Exp Ophthalmol. 2024 Dec;262(12):3971-3978. doi: 10.1007/s00417-024-06582-y. Epub 2024 Jul 29.
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.
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.
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).
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.
本研究旨在比较初治的新生血管性年龄相关性黄斑变性(nAMD)患者接受法西单抗或阿柏西普治疗的疗效,采用倾向评分匹配(PSM)来平衡患者背景。
本研究纳入了初治的nAMD患者,这些患者在负荷期接受了连续三个月每月一次的法西单抗或阿柏西普注射。在1:1的PSM中,选择性别、年龄、最佳矫正视力(BCVA)、中心黄斑厚度(CMT)、中心脉络膜厚度(CCT)以及治疗前状态下的AMD亚型作为协变量。我们在首次注射后的1、2和3个月检查了BCVA、CMT、CCT和残留液体积聚情况。
PSM后,法西单抗组和阿柏西普组各纳入43只眼。与基线相比,两组在初次注射后的1、2和3个月时BCVA、CMT和CCT均有显著改善。同时,两组在任何时间点的BCVA、CMT和CCT方面均未观察到显著差异。在1个月时,法西单抗组18.6%的患者和阿柏西普组41.9%的患者出现视网膜下液或视网膜内液残留,两组间存在显著差异(P = 0.03)。
法西单抗和阿柏西普进行三次负荷注射后BCVA均有所改善。在日本队列中,法西单抗在减少视网膜下液方面可能提供良好的早期治疗反应。