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TENAYA and LUCERNE: Two-Year Results from the Phase 3 Neovascular Age-Related Macular Degeneration Trials of Faricimab with Treat-and-Extend Dosing in Year 2.泰尼雅和卢塞恩:贝伐珠单抗生物类似药 faricimab 在湿性年龄相关性黄斑变性 2 年治疗和延长给药的 3 期临床试验的 2 年结果。
Ophthalmology. 2024 Aug;131(8):914-926. doi: 10.1016/j.ophtha.2024.02.014. Epub 2024 Feb 19.
2
One-year results of treat-and-extend regimen with intravitreal faricimab for treatment-naïve neovascular age-related macular degeneration.治疗初发新生血管性年龄相关性黄斑变性的玻璃体腔内 faricimab 按需治疗方案的一年疗效。
Jpn J Ophthalmol. 2024 Mar;68(2):83-90. doi: 10.1007/s10384-023-01040-4. Epub 2024 Jan 20.
3
INCIDENCE AND RISK FACTORS OF INTRAOCULAR INFLAMMATION AFTER BROLUCIZUMAB TREATMENT IN JAPAN: A Multicenter Age-Related Macular Degeneration Study.日本博鲁力单抗治疗后眼内炎症的发生率和危险因素:一项多中心年龄相关性黄斑变性研究。
Retina. 2024 Apr 1;44(4):714-722. doi: 10.1097/IAE.0000000000004009.
4
Comparison of functional and morphologic changes between brolucizumab and faricimab in neovascular age-related macular degeneration.布罗利珠单抗和法西单抗在新生血管性年龄相关性黄斑变性中的功能和形态学变化比较。
Graefes Arch Clin Exp Ophthalmol. 2024 Feb;262(2):589-599. doi: 10.1007/s00417-023-06241-8. Epub 2023 Sep 26.
5
Efficacy, durability, and safety of faricimab in patients from Asian countries with neovascular age-related macular degeneration: 1-Year subgroup analysis of the TENAYA and LUCERNE trials.法西单抗治疗亚洲国家新生血管性年龄相关性黄斑变性患者的疗效、持久性和安全性:TENAYA和LUCERNE试验的1年亚组分析
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6
Current and Novel Therapeutic Approaches for Treatment of Neovascular Age-Related Macular Degeneration.当前和新型治疗方法治疗新生血管性年龄相关性黄斑变性。
Biomolecules. 2022 Nov 3;12(11):1629. doi: 10.3390/biom12111629.
7
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Treat-and-Extend Regimens for the Management of Neovascular Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy: Consensus and Recommendations From the Asia-Pacific Vitreo-retina Society.用于治疗新生血管性年龄相关性黄斑变性和息肉样脉络膜血管病变的治疗与延长方案:亚太玻璃体视网膜学会的共识与建议
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初治新生血管性年龄相关性黄斑变性患者玻璃体内注射法西单抗的一年疗效

One-Year Outcomes of Intravitreal Faricimab Injection in Treatment-Naïve Patients With Neovascular Age-Related Macular Degeneration.

作者信息

Okawa Kazuyoshi, Maruyama-Inoue Maiko, Chin Jacob Yuhang, Inoue Tatsuya, Yanagi Yasuo, Kadonosono Kazuaki

机构信息

Department of Ophthalmology, Yokohama City University Medical Center, Yokohama, Japan.

National Healthcare Group Eye Institute, Tan Tock Seng Hospital, Singapore.

出版信息

J Vitreoretin Dis. 2025 Jul 20:24741264251352888. doi: 10.1177/24741264251352888.

DOI:10.1177/24741264251352888
PMID:40698349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12277302/
Abstract

To investigate the 1-year functional and morphologic outcomes of intravitreal (IVT) faricimab in treatment-naïve Japanese patients with neovascular age-related macular degeneration (nAMD). A retrospective study was performed to examine the outcomes of patients with nAMD who received IVT faricimab using a treat-and-extend regimen. The best-corrected visual acuity (BCVA), central foveal thickness (CFT), central choroidal thickness, dry macular achievement, and treatment intervals at 48 weeks were evaluated. Furthermore, the presence of polypoidal lesions at 48 weeks, as indicated by indocyanine green angiography, was investigated in patients with polypoidal choroidal vasculopathy (PCV). This study included 48 Japanese treatment-naïve patients with nAMD assessed at 1 year of follow-up. The BCVA was significantly improved 1 year after initial treatment ( < .001). CFT and central choroidal thickness were also significantly decreased after 1 year ( < .001 and < .001, respectively). Dry macula was achieved in 42 eyes (87.5%), and the mean (±SD) treatment interval at 12 months was 14.5 ± 4.4 weeks. The 1-year polyp regression rate was 76.9% (10/13 eyes). IVT faricimab was well tolerated and appeared to improve both functional and anatomic outcomes in Japanese patients with nAMD. In addition, a high rate of polyp regression was seen in patients with PCV.

摘要

研究玻璃体内注射法西单抗对初治日本新生血管性年龄相关性黄斑变性(nAMD)患者的1年功能和形态学结局。进行一项回顾性研究,以检查接受玻璃体内注射法西单抗并采用治疗并延长方案的nAMD患者的结局。评估了48周时的最佳矫正视力(BCVA)、中心凹厚度(CFT)、脉络膜中央厚度、干性黄斑实现情况和治疗间隔。此外,对息肉样脉络膜血管病变(PCV)患者,通过吲哚菁绿血管造影研究了48周时息肉样病变的存在情况。本研究纳入了48例初治日本nAMD患者,随访1年。初始治疗1年后BCVA显著改善(<.001)。1年后CFT和脉络膜中央厚度也显著降低(分别为<.001和<.001)。42只眼(87.5%)实现了干性黄斑,12个月时的平均(±标准差)治疗间隔为14.5±4.4周。1年时息肉消退率为76.9%(10/13只眼)。玻璃体内注射法西单抗耐受性良好,似乎可改善日本nAMD患者的功能和解剖学结局。此外,PCV患者的息肉消退率很高。