Academic Unit of Ophthalmology, York and Scarborough Teaching Hospitals NHS Foundation Trust, York, UK.
Hull York Medical School, University of York, York, UK.
Acta Ophthalmol. 2024 May;102(3):e328-e338. doi: 10.1111/aos.15774. Epub 2023 Sep 30.
Data are limited pertaining to the long-term benefits of aflibercept treatment for neovascular age-related macular degeneration (nAMD). The aim of this study was to provide outcomes, safety, durability and quality-of-life data with aflibercept using a modified treat, extend and fixed regime over 4 years.
Prospective, multicentre, single cohort observational study of treatment-naïve nAMD participants treated with aflibercept as 2-year extension of the MATE-trial that compared early and late Treat-and-Extend for 2 years. Refracted ETDRS best corrected visual acuity (BCVA), central retinal thickness (CRT), treatment interval and adverse events were assessed. Quality-of-life was measured using the Macular Disease Dependent Quality of Life (MacDQoL) and Macular Disease Treatment Satisfaction Questionnaires (MacTSQ).
Twenty-six of 40 participants completing the MATE-trial were enrolled with 20 completing the total 4-year study. Mean BCVA was 60.7 at Month 0 and 64.8 ETDRS letters at Month 48 while CRT decreased from 423.7 μm to 292.2 μm. Five participants discontinued treatment due to inactivity. The mean number of treatments and visits for the remaining participants was 27 and 30.0, respectively, with treatment intervals extended to 12 weeks in four participants at Month 48. Both AMD-specific QoL and treatment satisfaction remained stable between Months 0 and 48 and mean BCVA significantly correlated with AMD-specific QoL scores at Months 12, 24 and 48.
Results suggest that BCVA can be maintained over 48 months when following a treat-extend-and-fix regimen of aflibercept with intervals out to 12 weeks, while maintaining AMD-specific QoL and treatment satisfaction.
有关抗血管内皮生长因子(VEGF)融合蛋白(aflibercept)治疗新生血管性年龄相关性黄斑变性(nAMD)的长期获益数据有限。本研究旨在提供 4 年中使用 aflibercept 采用改良的“治疗-延长-固定”方案的治疗结局、安全性、持久性和生活质量数据。
这是一项前瞻性、多中心、单队列观察性研究,纳入了接受 aflibercept 治疗的初治 nAMD 患者,这些患者是 MATE 试验的 2 年扩展研究对象,该试验比较了早期和晚期“治疗-延长”方案治疗 2 年的疗效。评估屈光度矫正最佳视力(BCVA)、中心视网膜厚度(CRT)、治疗间隔和不良事件。使用黄斑疾病依赖生活质量量表(MacDQoL)和黄斑疾病治疗满意度问卷(MacTSQ)评估生活质量。
在完成 MATE 试验的 40 名患者中,有 26 名入组,其中 20 名完成了总计 4 年的研究。在 0 个月时,平均 BCVA 为 60.7 个字母,在 48 个月时为 64.8 个字母,而 CRT 从 423.7μm 下降到 292.2μm。有 5 名患者因病情无活动而停止治疗。其余患者的平均治疗次数和就诊次数分别为 27 次和 30.0 次,在 48 个月时,4 名患者的治疗间隔延长至 12 周。在 0 个月和 48 个月时,AMD 特异性生活质量和治疗满意度均保持稳定,平均 BCVA 在 12、24 和 48 个月时与 AMD 特异性生活质量评分显著相关。
结果表明,当采用 aflibercept 的“治疗-延长-固定”方案治疗时,治疗间隔可延长至 12 周,在 48 个月时可维持 BCVA,并保持 AMD 特异性生活质量和治疗满意度。