Shen Mengxi, Berni Alessandro, Liu Jeremy, Hiya Farhan, Herrera Gissel, El-Mulki Omar S, Beqiri Sara, Cheng Yuxuan, Kastner James, Trivizki Omer, Kumar Sivathanu, Zhang Yi, Le Viet Hoan, O'Brien Robert C, Nicola Maura Di, Yehoshua Zohar, Dubovy Sander R, Wang Ruikang K, Gregori Giovanni, Rosenfeld Philip J
Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, USA; Department of Ophthalmology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Am J Ophthalmol. 2025 Sep 5. doi: 10.1016/j.ajo.2025.09.006.
To report on the real-world experience of using intravitreal pegcetacoplan for the treatment of geographic atrophy (GA) in age-related macular degeneration (AMD).
Retrospective interventional case series.
Eyes with symptomatic GA secondary to AMD were treated with 15mg of intravitreal pegcetacoplan and participated in an ongoing prospective swept-source optical coherence tomography angiography (SS-OCTA) imaging study. All eyes underwent SS-OCTA imaging before and during pegcetacoplan therapy to assess for GA lesion size, the presence of non-exudative macular neovascularization (MNV), and the onset of exudation. The growth rate of GA and best-corrected visual acuity (BCVA) were assessed for eyes followed for 1 year.
From April 12, 2023, to November 11, 2024, 154 eyes were injected with pegcetacoplan, and 103 eyes had 1-year follow-up. At baseline, 11 eyes had been previously treated with anti-VEGF therapy, and 9 eyes were diagnosed with treatment-naïve non-exudative MNV by SS-OCTA. Each eye received an average of 10±2 injections, with an average interval of 1.2 months between injections. For the 97 eyes with 1 year of follow-up and measurable GA, the square-root (sqrt) GA growth rate after pegcetacoplan treatment was 0.24±0.15 mm/year. Of these 97 eyes, 63 eyes had prior annual visits before pegcetacoplan treatment was started. In these eyes, the annual sqrt GA growth rate was 0.33±0.22 mm/year before pegcetacoplan and 0.21±0.12 mm/year after pegcetacoplan, resulting in a 37% decrease in the growth rate (p<0.001). There were no significant differences in GA growth rate between foveal and non-foveal GA, either before or after the use of pegcetacoplan (all p≥0.80). The mean BCVA declined from 63±14 to 59±15 letters over one year (p=0.001), with no significant difference between foveal and non-foveal GA (p=0.36). Among the 29 eyes developing exudation during pegcetacoplan treatment, 19 (66%) had no evidence of any detectable MNV at baseline and during treatment on SS-OCTA.
Eyes treated with pegcetacoplan after 1 year had a 37% reduction in GA growth rate compared with their prior annual growth rate. Pegcetacoplan slowed the growth for foveal and non-foveal GA at a similar rate. Most of the pegcetacoplan-associated exudation was not due to detectable MNV.
报告玻璃体内注射培西加可兰治疗年龄相关性黄斑变性(AMD)所致地图样萎缩(GA)的真实世界经验。
回顾性干预病例系列。
对继发于AMD的有症状GA的眼睛,用15mg玻璃体内培西加可兰进行治疗,并参与一项正在进行的前瞻性扫频源光学相干断层扫描血管造影(SS-OCTA)成像研究。所有眼睛在培西加可兰治疗前和治疗期间均接受SS-OCTA成像,以评估GA病变大小、非渗出性黄斑新生血管(MNV)的存在情况以及渗出的发生情况。对随访1年的眼睛评估GA的生长速率和最佳矫正视力(BCVA)。
从2023年4月12日至2024年11月11日,154只眼睛接受了培西加可兰注射,103只眼睛进行了1年的随访。基线时,11只眼睛先前接受过抗VEGF治疗,9只眼睛经SS-OCTA诊断为未经治疗的非渗出性MNV。每只眼睛平均接受10±2次注射,注射间隔平均为1.2个月。对于97只随访1年且GA可测量的眼睛,培西加可兰治疗后GA的平方根(sqrt)生长速率为0.24±0.15mm/年。在这97只眼睛中,63只眼睛在开始培西加可兰治疗前有年度检查数据。在这些眼睛中,培西加可兰治疗前GA的年度sqrt生长速率为0.33±0.22mm/年,治疗后为0.21±0.12mm/年,生长速率降低了37%(p<0.001)。使用培西加可兰前后,黄斑中心凹和非黄斑中心凹GA的生长速率均无显著差异(所有p≥0.80)。1年中平均BCVA从63±14下降至59±15字母(p=0.001),黄斑中心凹和非黄斑中心凹GA之间无显著差异(p=0.36)。在培西加可兰治疗期间发生渗出的29只眼睛中,19只(66%)在基线和治疗期间的SS-OCTA检查中未发现任何可检测到的MNV证据。
接受培西加可兰治疗1年后的眼睛,其GA生长速率与之前的年度生长速率相比降低了37%。培西加可兰以相似的速率减缓了黄斑中心凹和非黄斑中心凹GA的生长。大多数与培西加可兰相关的渗出并非由可检测到的MNV引起。