Faricimab在日本治疗糖尿病黄斑水肿的两年真实世界结果

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-08-29 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S547179
Yuki Mizuki, Soichiro Inokuchi, Tsubasa Kuroki, Akihiro Kamata, Junji Onishi, Yoshiko Watanabe, Masato Takeda, Akira Meguro, Tatsukata Kawagoe, Takeshi Teshigawara, Norihiro Yamada, Nobuhisa Mizuki
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引用次数: 0

摘要

背景:糖尿病性黄斑水肿(DME)是工作年龄成人视力丧失的主要原因。Faricimab是一种靶向VEGF和Ang-2的双特异性抗体,已被证明可以通过延长注射间隔来减轻治疗负担。然而,现实世界中来自日本人口的长期数据是有限的。目的:在日本真实世界的临床环境中评估玻璃体内法利西单抗治疗二甲醚的两年疗效和安全性。方法:本回顾性观察研究在日本横滨国际亲善医院进行。采用玻璃体内法昔单抗治疗后随访两年的DME患者。结果测量包括中心亚野厚度(CST)、最佳矫正视力(BCVA)、黄斑液分辨率和复发率。使用非参数检验和生存分析评估变化。结果:我们分析了9例DME患者(16只眼),他们在玻璃体内注射法利西单抗后随访了两年。除了一种情况外,所有情况都省略了四次注射加载阶段,中位数为一次初始注射。CST从332.3µm下降到267.0µm (p = 0.069), BCVA保持稳定(0.49 ~ 0.55 logMAR, p = 0.2081)。黄斑液完全溶解率为87.5%,中位溶解时间为6个月。随访期间有37.5%的眼睛复发,中位复发时间为9个月。在固定给药组(n = 11)中,72.7%的患者最终注射间隔≥12周。视网膜内液(IRF)显著降低(p = 0.0078),慢性囊样改变与有限的CST降低相关(p = 0.016)。未见治疗相关不良事件的报道。结论:尽管在大多数情况下省略了加载阶段,但Faricimab在现实环境中表现出良好的解剖效果,并延长了两年以上的注射间隔。这些发现支持了faricimab在日本二甲醚治疗中的实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Two-Year Real-World Outcomes of Faricimab for Diabetic Macular Edema in Japan.

Two-Year Real-World Outcomes of Faricimab for Diabetic Macular Edema in Japan.

Two-Year Real-World Outcomes of Faricimab for Diabetic Macular Edema in Japan.

Background: Diabetic macular edema (DME) is a leading cause of vision loss in working-age adults. Faricimab, a bispecific antibody targeting VEGF and Ang-2, has been shown to reduce treatment burden by enabling extended injection intervals. However, real-world, long-term data from Japanese populations are limited.

Purpose: To evaluate the two-year efficacy and safety of intravitreal faricimab for DME in a real-world clinical setting in Japan.

Methods: This retrospective observational study was conducted at the International Goodwill Hospital, Yokohama, Japan. Patients with DME who were followed for two years after initiating intravitreal faricimab. Outcome measures included central subfield thickness (CST), best-corrected visual acuity (BCVA), macular fluid resolution, and recurrence. Changes were evaluated using nonparametric tests and survival analysis.

Results: We analyzed 9 patients (16 eyes) with DME who were followed for two years after initiating intravitreal faricimab. A four-injection loading phase was omitted in all but one case, with a median of one initial injection. CST decreased from 332.3 µm to 267.0 µm (p = 0.069), and BCVA remained stable (0.49 to 0.55 logMAR, p = 0.2081). Complete macular fluid resolution occurred in 87.5% of eyes, with a median resolution time of 6 months. Recurrence occurred in 37.5% of eyes during follow-up, with a median time to recurrence of 9 months. Among eyes on fixed dosing (n = 11), 72.7% achieved a final injection interval of ≥12 weeks. Intraretinal fluid (IRF) significantly decreased (p = 0.0078), and chronic cystoid changes were associated with limited CST reduction (p = 0.016). No treatment-related adverse events were reported.

Conclusion: Faricimab demonstrated favorable anatomical outcomes and extended injection intervals over two years in a real-world setting, despite the omission of a loading phase in most cases. These findings support its practical utility of faricimab for DME management in Japan.

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