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Real-world faricimab switch in France: artificial intelligence-based detection of changes in exudative signs in difficult-to-treat neovascular age-related macular degeneration.法国现实世界中阿柏西普的转换:基于人工智能检测难治性新生血管性年龄相关性黄斑变性渗出体征的变化
BMJ Open Ophthalmol. 2025 Jun 23;10(1):e002267. doi: 10.1136/bmjophth-2025-002267.
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Switching to Faricimab in Therapy-Resistant Macular Edema Due to Retinal Vein Occlusion: Initial Real-World Efficacy Outcomes.视网膜静脉阻塞所致治疗抵抗性黄斑水肿转换为使用法西单抗治疗:初始真实世界疗效结果
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本文引用的文献

1
Initial Real-World Experience with Faricimab in Treatment-Resistant Neovascular Age-Related Macular Degeneration.法西单抗治疗难治性新生血管性年龄相关性黄斑变性的初步真实世界经验
Clin Ophthalmol. 2023 May 5;17:1287-1293. doi: 10.2147/OPTH.S409822. eCollection 2023.
2
The real-world efficacy and safety of faricimab in neovascular age-related macular degeneration: the TRUCKEE study - 6 month results.法瑞西单抗在新生血管性年龄相关性黄斑变性中的真实世界疗效和安全性:TRUCKEE 研究 - 6 个月结果。
Eye (Lond). 2023 Dec;37(17):3574-3581. doi: 10.1038/s41433-023-02553-5. Epub 2023 May 12.
3
High-Dose Aflibercept for Neovascular AMD and DME in Suboptimal Responders to Standard-Dose Aflibercept.高剂量阿柏西普用于对标准剂量阿柏西普反应欠佳的新生血管性年龄相关性黄斑变性和糖尿病性黄斑水肿患者
J Vitreoretin Dis. 2023 Feb 15;7(2):116-124. doi: 10.1177/24741264221150345. eCollection 2023 Mar-Apr.
4
Faricimab in neovascular AMD: first report of real-world outcomes in an independent retina clinic.法西单抗治疗新生血管性年龄相关性黄斑变性:独立视网膜诊所真实世界结局的首次报告。
Eye (Lond). 2023 Oct;37(15):3282-3289. doi: 10.1038/s41433-023-02505-z. Epub 2023 Mar 23.
5
Spotlight on Faricimab in the Treatment of Wet Age-Related Macular Degeneration: Design, Development and Place in Therapy.聚焦法西单抗治疗湿性年龄相关性黄斑变性:设计、研发及治疗定位。
Drug Des Devel Ther. 2022 Sep 29;16:3395-3400. doi: 10.2147/DDDT.S368963. eCollection 2022.
6
Aflibercept versus Faricimab in the Treatment of Neovascular Age-Related Macular Degeneration and Diabetic Macular Edema: A Review.阿柏西普与 faricimab 在新生血管性年龄相关性黄斑变性和糖尿病性黄斑水肿治疗中的比较:综述。
Int J Mol Sci. 2022 Aug 20;23(16):9424. doi: 10.3390/ijms23169424.
7
Faricimab: First Approval.法西单抗:首次获批。
Drugs. 2022 May;82(7):825-830. doi: 10.1007/s40265-022-01713-3.
8
Efficacy, durability, and safety of intravitreal faricimab up to every 16 weeks for neovascular age-related macular degeneration (TENAYA and LUCERNE): two randomised, double-masked, phase 3, non-inferiority trials.玻璃体腔内 faricimab 每 16 周治疗新生血管性年龄相关性黄斑变性的疗效、持久性和安全性(TENAYA 和 LUCERNE):两项随机、双盲、3 期、非劣效性试验。
Lancet. 2022 Feb 19;399(10326):729-740. doi: 10.1016/S0140-6736(22)00010-1. Epub 2022 Jan 24.
9
Faricimab: expanding horizon beyond VEGF.法西单抗:超越血管内皮生长因子的拓展视野。
Eye (Lond). 2020 May;34(5):802-804. doi: 10.1038/s41433-019-0670-1. Epub 2019 Nov 6.
10
Epidemiology of age-related macular degeneration (AMD): associations with cardiovascular disease phenotypes and lipid factors.年龄相关性黄斑变性(AMD)的流行病学:与心血管疾病表型和脂质因素的关联
Eye Vis (Lond). 2016 Dec 22;3:34. doi: 10.1186/s40662-016-0063-5. eCollection 2016.

新生血管性年龄相关性黄斑变性患者对抗VEGF治疗反应欠佳转而使用法西单抗后的视觉和解剖学反应

Visual and Anatomic Responses in Patients With Neovascular Age-Related Macular Degeneration and a Suboptimal Response to Anti-VEGF Therapy Switched to Faricimab.

作者信息

Khodor Ali, Choi Stephanie, Nanda Tavish, Caranfa Jonathan T, Ruiz-Lozano Raul E, Desai Shilpa H, Liang Michelle, Baumal Caroline R, Reed David C, Cleary Tina S, Heier Jeffrey S, Shah Chirag P, Witkin Andre J

机构信息

Bascom Palmer Eye Institute, University of Miami, Miami, FL, USA.

New England Eye Center, Tufts University Medical Center, Boston, MA, USA.

出版信息

J Vitreoretin Dis. 2024 Aug 31:24741264241271649. doi: 10.1177/24741264241271649.

DOI:10.1177/24741264241271649
PMID:39554629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11562232/
Abstract

To determine the efficacy of switching to intravitreal (IVT) faricimab in patients with treatment-resistant neovascular age-related macular degeneration (nAMD) and determine the rates of reversion to original antivascular endothelial growth factor (anti-VEGF) therapy. A retrospective chart review was performed of patients with nAMD and persistent fluid on optical coherence tomography previously treated with anti-VEGF injections who received at least 1 IVT faricimab injection between March 1, 2022, and January 31, 2023. The study comprised 135 eyes of 119 patients. Before switching to IVT faricimab, the mean number of anti-VEGF injections in the previous 12 months was 10.7 ± 2.6 (SD) with a mean interval of 4.8 ± 1.3 weeks (range, 2-8). The mean follow-up was 11.6 ± 2 months. Thirty eyes (22.2%) switched to IVT faricimab returned to the original therapy. Of 105 eyes remaining on IVT faricimab, 66 (62.9%) had no fluid at the last follow-up. Compared with the original treatment, there was a significant improvement in logMAR visual acuity at the last follow-up in eyes on IVT faricimab (0.42 vs 0.38;  < .01) and in central subfield thickness (286 µm vs 246 µm;  < .0001). There was also a significant increase in the dosing interval after the third injection vs before IVT faricimab was prescribed (4.8 weeks vs 5.5 weeks;  < .001). Faricimab has a potent drying effect and potential for increasing the injection interval in many eyes with nAMD and persistent fluid on other anti-VEGF agents. Although nearly 25% of eyes reverted to the original therapy because of an insufficient response or adverse events, the majority did not achieve fluid resolution after reversion.

摘要

确定转换为玻璃体内注射法西单抗对治疗抵抗性新生血管性年龄相关性黄斑变性(nAMD)患者的疗效,并确定恢复原抗血管内皮生长因子(anti-VEGF)治疗的比例。对nAMD且光学相干断层扫描显示有持续性积液、此前接受过anti-VEGF注射治疗、在2022年3月1日至2023年1月31日期间接受至少1次玻璃体内注射法西单抗的患者进行回顾性病历审查。该研究纳入了119例患者的135只眼。转换为玻璃体内注射法西单抗之前,前12个月anti-VEGF注射的平均次数为10.7±2.6(标准差),平均间隔为4.8±1.3周(范围2 - 8周)。平均随访时间为11.6±2个月。转换为玻璃体内注射法西单抗的30只眼(22.2%)恢复了原治疗。在继续接受玻璃体内注射法西单抗的105只眼中,66只眼(62.9%)在最后一次随访时无积液。与原治疗相比,接受玻璃体内注射法西单抗的眼在最后一次随访时的logMAR视力有显著改善(0.42对0.38;P < 0.01),中心子场厚度也有显著改善(286 µm对246 µm;P < 0.0001)。与开具玻璃体内注射法西单抗之前相比,第三次注射后的给药间隔也显著延长(4.8周对5.5周;P < 0.001)。法西单抗对许多患有nAMD且在使用其他anti-VEGF药物时有持续性积液的眼有强大的积液清除作用和延长注射间隔的潜力。尽管近25%的眼因反应不足或不良事件恢复了原治疗,但大多数眼恢复原治疗后未实现积液清除。