Visual outcome following initiation of first injection versus after three monthly doses of aflibercept 2 mg for treatment naïve age-related macular degeneration to inform clinical trial designs: PRECISE Report No. 6.

IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye Pub Date : 2025-05-12 DOI:10.1038/s41433-025-03797-z
Swati Chandak, Sarega Gurudas, Raheeba Pakeer Muhammed, Ayse Keskin, Sridevi Thottarath, Faruque Ghanchi, Anna Grabowska, Stephen James Talks, Ian Pearce, Martin McKibbin, Ajay Kotagiri, Geeta Menon, Benjamin J L Burton, Richard Gale, Sobha Sivaprasad
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引用次数: 0

Abstract

Purpose: To study the outcome of the first dose versus three monthly doses of 2 mg aflibercept in the initiation phase of neovascular age-related macular degeneration (nAMD) to inform future clinical trial design on novel durable agents. These agents may take time to act and so initial dosing with aflibercept 2 mg is required for immediate effect.

Methods: Visual acuity (VA) outcomes and associations with baseline VA and OCT characteristics were analysed using logistic regression via generalised estimating equations. In addition, VA outcomes based on different combinations of eligibility criteria were assessed.

Results: A total of 1999 eyes of 1862 patients were analysed. The mean age was 79.3 (SD 7.8) years. The mean presenting VA was 58.0 (SD 14.5) ETDRS letter score. A statistical difference in VA was found after first injection (visit 2, 61.6, SD 14.3 ETDRS letter score) and after three monthly injections (visit 4, 62.7, SD 14.9 ETDRS letter score) (P < 0.001). Lower baseline VA and OCT features suggestive of structural changes in the fovea are associated with lower VA after both first and post- initiating doses. Eyes with baseline VA > / = 54 letters alone had similar VA outcomes to eyes with both VA > / = 54 letters and central subfield thickness (CST) of <500 microns.

Conclusion: Mean VA outcomes after three monthly anti-VEGF injections are significantly better than after the first initiating dose. However, baseline OCT characteristics associated with VA in these two timepoints are not clinically different.

第一次注射后的视力结果与三个月剂量2毫克阿伯西普治疗naïve年龄相关性黄斑变性临床试验设计:精确报告6号。
目的:研究在新生血管性年龄相关性黄斑变性(nAMD)起始阶段,首次给药与3个月给药2mg阿伯西普的疗效,为未来新型长效药物的临床试验设计提供信息。这些药物可能需要一段时间才能起作用,因此初始剂量为2毫克的阿伯西普才能立即起作用。方法:通过广义估计方程,采用logistic回归分析视力(VA)结果及其与基线VA和OCT特征的关系。此外,评估了基于不同资格标准组合的VA结果。结果:对1862例患者1999只眼进行了分析。平均年龄79.3岁(SD 7.8)。平均表现VA为58.0 (SD 14.5) ETDRS字母评分。第一次注射后(就诊2,61.6,SD 14.3 ETDRS字母评分)和三个月注射后(就诊4,62.7,SD 14.9 ETDRS字母评分)(P / = 54字母)的VA结果与VA > / = 54字母和中心子场厚度(CST)的眼睛相似)有统计学差异。结论:三个月注射抗vegf后的平均VA结果明显优于第一次起始剂量后。然而,这两个时间点与VA相关的基线OCT特征在临床上并无差异。
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来源期刊
Eye
Eye 医学-眼科学
CiteScore
6.40
自引率
5.10%
发文量
481
审稿时长
3-6 weeks
期刊介绍: Eye seeks to provide the international practising ophthalmologist with high quality articles, of academic rigour, on the latest global clinical and laboratory based research. Its core aim is to advance the science and practice of ophthalmology with the latest clinical- and scientific-based research. Whilst principally aimed at the practising clinician, the journal contains material of interest to a wider readership including optometrists, orthoptists, other health care professionals and research workers in all aspects of the field of visual science worldwide. Eye is the official journal of The Royal College of Ophthalmologists. Eye encourages the submission of original articles covering all aspects of ophthalmology including: external eye disease; oculo-plastic surgery; orbital and lacrimal disease; ocular surface and corneal disorders; paediatric ophthalmology and strabismus; glaucoma; medical and surgical retina; neuro-ophthalmology; cataract and refractive surgery; ocular oncology; ophthalmic pathology; ophthalmic genetics.
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