视网膜色素上皮和外层视网膜萎缩(cRORA)进展:GATHER1 试验的事后分析。

IF 2.4 3区 医学 Q2 OPHTHALMOLOGY
Giulia Corradetti, Ayesha Karamat, Sowmya Srinivas, Sophiana Lindenberg, Swetha B Velaga, Federico Corvi, Yamini Attiku, Muneeswar Gupta Nittala, Dhaval Desai, Liansheng Zhu, Dina Abulon, SriniVas R Sadda
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引用次数: 0

摘要

目的:确定接受阿伐酸培高丸(ACP)治疗的地理性萎缩(GA)患者从不完全性视网膜色素上皮和外层视网膜萎缩(iRORA)发展为完全性视网膜色素上皮和外层视网膜萎缩(cRORA)的比率,以及从色素沉着发展为 iRORA/cRORA 的比率:GATHER1前瞻性、随机、双掩蔽II/III期研究的事后分析,该研究评估了ACP 2毫克与假性对比。来自 GATHER1 的光学相干断层扫描 (OCT) 数据被转移到多尼图像阅读和研究实验室,由对萎缩分类会议(CAM)分级特征有经验的阅读者进行掩蔽分析。在基线和第 6、12 和 18 个月时,对距离 GA 病变边界 500 µm 以上的 OCT 容量扫描区域进行评估。基线时有 iRORA 和/或色素(在 OCT 上高度≥ 40 µm)的参与者被纳入分析:结果:在第 6、12 和 18 个月时,ACP 2 mg 组从 iRORA 发展到 cRORA 的眼球比例分别为 5.0%、15.0% 和 20.0%,而假体组分别为 11.8%、30.2% 和 41.8%。在第6、12和18个月时,经ACP 2毫克治疗的眼球从玻璃体混浊发展为iRORA或cRORA的比例分别为3.8%、7.6%和7.6%,而假性治疗眼球的这一比例分别为15.9%、18.1%和27.2%:结论:与假性治疗相比,接受 ACP 2 mg 治疗的眼球从 iRORA 发展到 cRORA 的比率以及从玻璃体混浊发展到 iRORA/cRORA 的比率都有所降低,而且随着时间的推移,组间的差异越来越大,这表明早期干预可能会延缓疾病的进展:试验注册:ClinicalTrials.gov identifier:NCT02686658.注册日期:2016年2月16日:注册日期:2016年2月16日:众所周知,地理萎缩是老年性黄斑变性(AMD)的一种晚期形式,会导致不可逆的视力丧失,是公共卫生领域尚未满足的重大需求。萎缩分类会议(CAM)小组根据光学相干断层扫描中受影响的解剖层,为晚期AMD病变推荐了一种新的命名方法。因此,引入了不完全视网膜色素上皮和视网膜外层萎缩(iRORA)和完全视网膜色素上皮和视网膜外层萎缩(cRORA)这两个术语(Guymer等人,Ophthalmology 127:394-409,2020;Sadda等人,Ophthalmology 125:537-548,2018)。新发现 GATHER1事后分析表明,与假性治疗相比,阿伐伐他汀匹格醇(ACP)2毫克治疗可在6、12和18个月内降低从iRORA发展为cRORA的眼球比例,以及从玻璃体混浊发展为iRORA或cRORA的眼球比例。这些研究结果表明,ACP 在延缓现有的前萎缩性 AMD 病变进展方面具有潜在的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progression to complete retinal pigment epithelium and outer retinal atrophy (cRORA): post hoc analysis of the GATHER1 trial.

Purpose: Determine rates of progression of incomplete retinal pigment epithelium and outer retinal atrophy (iRORA) to complete retinal pigment epithelium and outer retinal atrophy (cRORA) and rates of progression of drusen to iRORA/cRORA in eyes with geographic atrophy (GA) treated with avacincaptad pegol (ACP).

Methods: Post hoc analysis of the GATHER1 prospective, randomized, double-masked Phase II/III study that evaluated ACP 2 mg vs. sham. Optical coherence tomography (OCT) data from GATHER1 were transferred to the Doheny Image Reading and Research Lab for masked analysis by readers experienced with Classification of Atrophy Meeting (CAM) grading features. Regions of OCT volume scans more than 500 µm from the border of GA lesions were evaluated at baseline and at months 6, 12, and 18. Participants with iRORA and/or drusen (≥ 40 µm height on OCT) at baseline were included in the analysis.

Results: The proportion of eyes progressing from iRORA to cRORA in the ACP 2 mg group was 5.0%, 15.0%, and 20.0% at months 6, 12, and 18 respectively, as compared with 11.8%, 30.2%, and 41.8% of eyes in the sham group. The proportion of ACP 2 mg-treated eyes progressing from drusen to iRORA or cRORA was 3.8%, 7.6%, and 7.6% at months 6, 12, and 18 compared with 15.9%, 18.1%, and 27.2% of sham-treated eyes.

Conclusions: Rates of progression from iRORA to cRORA and drusen to iRORA/cRORA were reduced in eyes treated with ACP 2 mg vs. sham, with increasing separation between groups over time, suggesting early intervention may slow disease progression.

Trial registration: ClinicalTrials.gov identifier: NCT02686658. Date of registration: February 16, 2016.

Key messages: What is known Geographic atrophy is an advanced form of age-related macular degeneration (AMD) that leads to irreversible vision loss, presenting a significant public health unmet need. The Classification of Atrophy Meeting (CAM) group recommended a new nomenclature for advanced AMD lesions, based on the affected anatomical layers on optical coherence tomography. Accordingly, the terms incomplete retinal pigment epithelium and outer retinal atrophy (iRORA) and complete retinal pigment epithelium and outer retinal atrophy (cRORA) were introduced (Guymer et al., Ophthalmology 127:394-409, 2020; Sadda et al., Ophthalmology 125:537-548, 2018). What is new GATHER1 post hoc analysis shows that treatment with avacincaptad pegol (ACP) 2 mg decreases the proportion of eyes that progress from iRORA to cRORA, and from drusen to iRORA or cRORA, compared with sham, over 6, 12, and 18 months. These findings suggest a potential role for ACP in delaying the progression of existing pre-atrophic AMD lesions.

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来源期刊
CiteScore
5.40
自引率
7.40%
发文量
398
审稿时长
3 months
期刊介绍: Graefe''s Archive for Clinical and Experimental Ophthalmology is a distinguished international journal that presents original clinical reports and clini-cally relevant experimental studies. Founded in 1854 by Albrecht von Graefe to serve as a source of useful clinical information and a stimulus for discussion, the journal has published articles by leading ophthalmologists and vision research scientists for more than a century. With peer review by an international Editorial Board and prompt English-language publication, Graefe''s Archive provides rapid dissemination of clinical and clinically related experimental information.
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