SIRE: Short interval in real life Does intensive anti-VEGF treatment in the first year predict subsequent treatment burden in exudative age-related macular degeneration?

IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye Pub Date : 2025-03-20 DOI:10.1038/s41433-025-03734-0
B Matagrin, I Fenniri, N Chirpaz, J Billant, E Agard, R Chudzinski, C Burillon, C Dot
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引用次数: 0

Abstract

Background: Anti-VEGF's have changed the prognosis of exudative age-related macular degeneration (AMD). Ranibizumab and aflibercept have proven their functional efficacy, but their use has revealed in real life a wide variety of patient profiles with varied responses to treatment. This work focused on patients receiving "intensive" IVT treatment with a sustained injection rhythm, also referred to as having a high treatment burden.

Objective: The main objective of this work was to determine, in real-life conditions, the proportion of patients receiving "intensive" treatment among those being followed for exudative AMD. Secondary objectives were to analyse the long-term functional outcomes of these patients, their anatomical characteristics, and the evolution of their treatment regimen.

Method: A retrospective descriptive single-centre real-life study was conducted on patients treated for exudative AMD with intensive treatment (intervals of less than 8 weeks during the first year of treatment). A subgroup analysis compared patients who exceeded Q8 during follow-up (Group 1) versus patients remaining in intensive treatment (Group 2).

Results: A total of 301 records were analysed, with 24.9% of the eyes (n = 75) considered under intensive treatment. The mean age was 84 years ( ± 7.5), and 61% were men. Type 1 choroidal neovascularization (CNV) accounted for 64% of our cohort, type 2 CNV represented 29.3%, and type 3 was involved in 6.7%. The mean follow-up was 5.6 years ( ± 3.6), with an average number of 41 IVT ( ± 26.7). Visual acuity was maintained at 0.53 ( ± 0.2) baseline vs. 0.61 ( ± 0.2) after 5 years of follow-up (p = 0.02). Central retinal thickness (CRT) and subretinal fluid (SRF) were significantly reduced during our follow-up, and PED height remained stable. Almost half of the eyes (44%) had an extension of their interval ( > Q8) beyond the first year; however, this objective was achieved on average after 4.5 years of treatment. The visual acuity of Group 2 ( < Q8), despite receiving more injections, was superior to that of Group 1 ( > Q8) with baseline values of 0.57 ( ± 0.2) and 0.48 ( ± 0.2) (p = 0.161) respectively, and at 5 years 0.79 ( ± 0.2) and 0.54 ( ± 0.2) (p = 0.026). Similarly, CRT, PED height, and SRF were higher in Group 2. The distribution of neovascular types showed more type 2 in Group 1 (45.5% vs. 16.7%).

Conclusion: Patients requiring intensive treatment represent about ¼ of our AMD patient population. Despite the high treatment burden, these patients maintain their visual acuity at 5 years. An extension of intervals is observed in nearly half of the patients, occurring late. Intensive treatment during the first year appears to be predictive of a future hight treatment burden.

第一年强化抗vegf治疗能否预测渗出性年龄相关性黄斑变性的后续治疗负担?
背景:抗vegf改变了渗出性年龄相关性黄斑变性(AMD)的预后。雷尼单抗和阿非利西普已经证明了它们的功能功效,但它们的使用在现实生活中揭示了各种各样的患者对治疗的不同反应。这项工作的重点是接受持续注射节奏的“强化”IVT治疗的患者,也被称为具有高治疗负担的患者。目的:这项工作的主要目的是确定,在现实生活条件下,接受“强化”治疗的患者在接受随访的渗出性AMD患者中所占的比例。次要目的是分析这些患者的长期功能结局、解剖特征和治疗方案的演变。方法:对接受强化治疗的渗出性AMD患者(治疗第一年间隔少于8周)进行回顾性描述性单中心现实研究。亚组分析比较了随访期间超过Q8的患者(第1组)和仍在强化治疗的患者(第2组)。结果:共分析了301例记录,其中24.9%的眼睛(n = 75)在强化治疗中。平均年龄84岁(±7.5岁),61%为男性。1型脉络膜新生血管(CNV)占我们队列的64%,2型CNV占29.3%,3型涉及6.7%。平均随访5.6年(±3.6年),平均IVT 41次(±26.7次)。随访5年后,视力维持在基线0.53(±0.2)和0.61(±0.2)(p = 0.02)。随访期间,视网膜中央厚度(CRT)和视网膜下液(SRF)明显减少,PED高度保持稳定。几乎一半(44%)的眼睛在第一年后的间隔时间延长(> Q8);然而,这一目标是在平均治疗4.5年后实现的。第2组(Q8)的视力基线值分别为0.57(±0.2)和0.48(±0.2)(p = 0.161),第5年的视力基线值分别为0.79(±0.2)和0.54(±0.2)(p = 0.026)。同样,第2组CRT、PED高度、SRF均较高。1组新生血管类型以2型为主(45.5% vs. 16.7%)。结论:需要强化治疗的患者约占AMD患者总数的四分之一。尽管治疗负担沉重,但这些患者在5年内仍能保持视力。在近一半的患者中观察到间隔延长,发生时间较晚。第一年的强化治疗似乎预示着未来的高治疗负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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