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培塞利珠单抗治疗与年龄相关的黄斑变性相关性地图状萎缩的 2 期随机临床试验

Complement C3 Inhibitor Pegcetacoplan for Geographic Atrophy Secondary to Age-Related Macular Degeneration: A Randomized Phase 2 Trial.

机构信息

Retina-Vitreous Associates Medical Group, Beverly Hills, California.

Apellis Pharmaceuticals, Inc, Waltham, Massachusetts.

出版信息

Ophthalmology. 2020 Feb;127(2):186-195. doi: 10.1016/j.ophtha.2019.07.011. Epub 2019 Jul 16.

Abstract

PURPOSE

Geographic atrophy (GA), a late stage of age-related macular degeneration (AMD), is a major cause of blindness. Even while central visual acuity remains relatively well preserved, GA often causes considerable compromise of visual function and quality of life. No treatment currently exists. We evaluated the safety and efficacy of pegcetacoplan, a complement C3 inhibitor, for treatment of GA.

DESIGN

Prospective, multicenter, randomized, sham-controlled phase 2 study.

PARTICIPANTS

Two hundred forty-six patients with GA.

METHODS

Patients with GA were assigned randomly in a 2:2:1:1 ratio to receive intravitreal injections of 15 mg pegcetacoplan monthly or every other month (EOM) or sham intravitreal injections monthly or EOM for 12 months with follow-up at months 15 and 18. Area and growth of GA were measured using fundus autofluorescence imaging.

MAIN OUTCOME MEASURES

The primary efficacy end point was mean change in square root GA lesion area from baseline to month 12. Secondary outcome measures included mean change from baseline in GA lesion area without the square root transformation, distance of GA lesion from the fovea, best-corrected visual acuity (BCVA), low-luminance BCVA, and low-luminance visual acuity deficit. The primary safety end point was the number and severity of treatment-emergent adverse events.

RESULTS

In patients receiving pegcetacoplan monthly or EOM, the GA growth rate was reduced by 29% (95% confidence interval [CI], 9-49; P = 0.008) and 20% (95% CI, 0-40; P = 0.067) compared with the sham treatment group. Post hoc analysis showed that the effect was greater in the second 6 months of treatment, with observed reductions of 45% (P = 0.0004) and 33% (P = 0.009) for pegcetacoplan monthly and EOM, respectively. Two cases of culture-positive endophthalmitis and 1 case of culture-negative endophthalmitis occurred in the pegcetacoplan monthly group. New-onset investigator-determined exudative AMD was reported more frequently in pegcetacoplan-treated eyes (18/86 eyes [20.9%] and 7/79 eyes [8.9%] in monthly and EOM groups, respectively) than in sham-treated eyes (1/81 eyes [1.2%]).

CONCLUSIONS

Local C3 inhibition with pegcetacoplan resulted in statistically significant reductions in the growth of GA compared with sham treatment. Phase 3 studies will define the efficacy and safety profile further.

摘要

目的

年龄相关性黄斑变性(AMD)晚期的地图状萎缩(GA)是失明的主要原因。即使中央视力相对较好,GA 通常也会导致相当大的视觉功能和生活质量受损。目前尚无治疗方法。我们评估了 pegcatacoplan(一种补体 C3 抑制剂)治疗 GA 的安全性和疗效。

设计

前瞻性、多中心、随机、假对照的 2 期研究。

参与者

246 名 GA 患者。

方法

GA 患者以 2:2:1:1 的比例随机分配接受每月或每隔一个月(EOM)玻璃体腔内注射 15mg pegcatacoplan 或每月或 EOM 接受假玻璃体腔内注射,随访至第 15 和 18 个月。使用眼底自发荧光成像测量 GA 病变面积和生长。

主要终点

从基线到第 12 个月时平方根 GA 病变面积的平均变化。次要终点包括从基线到 GA 病变面积的平均变化,不进行平方根转换,GA 病变与黄斑的距离,最佳矫正视力(BCVA),低亮度 BCVA 和低亮度视力缺陷。主要安全性终点是治疗后出现的不良事件的数量和严重程度。

结果

在接受 pegcatacoplan 每月或 EOM 治疗的患者中,GA 的生长速度分别降低了 29%(95%置信区间 [CI],9-49;P=0.008)和 20%(95%CI,0-40;P=0.067)与假治疗组相比。事后分析显示,在治疗的第二个 6 个月中效果更大,每月 pegcatacoplan 观察到的减少分别为 45%(P=0.0004)和 33%(P=0.009),EOM 分别为 33%(P=0.009)。每月 pegcatacoplan 组发生 2 例培养阳性眼内炎和 1 例培养阴性眼内炎。新发生的研究者确定的渗出性 AMD 在 pegcatacoplan 治疗的眼中更为常见(每月和 EOM 组分别为 86 眼中的 18/86 眼[20.9%]和 79 眼中的 7/79 眼[8.9%]),而假治疗组为 81 眼中的 1/81 眼[1.2%])。

结论

与假治疗相比,pegcatacoplan 局部 C3 抑制可使 GA 的生长速度明显降低。进一步的 3 期研究将确定其疗效和安全性。

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