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
Bascom Palmer Eye Institute, University of Miami, Miami, FL, USA.
New England Eye Center, Tufts University Medical Center, Boston, MA, USA.
J Vitreoretin Dis. 2024 Aug 31:24741264241271649. doi: 10.1177/24741264241271649.
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.
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。