Faricimab对1型黄斑新生血管的疗效:ai辅助量化Naïve和switch眼12个月内色素上皮脱离(PED)体积减少。

IF 1.9 Q2 OPHTHALMOLOGY
Jennifer Cattaneo, Paolo Forte, Giovanni Forte, Chiara M Eandi
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引用次数: 0

摘要

背景:本研究评估玻璃体内Faricimab在减少色素上皮脱离(PED)和液体体积方面的疗效treatment-naïve眼和对抗vegf单药治疗无反应的眼,所有被诊断为1型黄斑新生血管(T1 MNV),为期12个月。方法:在瑞士洛桑的Jules Gonin眼科医院进行了一项回顾性、单中心队列研究。回顾了2022年9月至2023年3月期间treatment-naïve和无应答切换患者继发于新生血管性年龄相关性黄斑变性(nAMD)的T1 MNV的临床记录。患者接受每月3次法利昔单抗注射的负荷剂量,随后进行治疗和延长(T&E)方案。在基线、3个月、6个月和12个月的随访中,采用多模式成像,包括结构OCT和人工智能辅助分析,量化PED体积和相关液体生物标志物。统计分析包括线性混合模型,以评估视网膜内(IRF)、视网膜下液(SRF)和PED体积的差异和趋势。结果:65例患者65只眼入组,其中女性占70.7%;平均年龄80.7岁,SD = 6.9岁)。80%的患者接受了抗vegf治疗(Switch组),20%的患者基线水平为treatment-Naïve。12个月时,Switch组玻璃体内治疗更频繁(平均次数= 8.3 vs. 6.0;p = 0.009)。随访12个月后,Naïve眼的BCVA得到改善(较基线增加6.9个ETDRS字母,p = 0.053), Switch眼的BCVA得到维持。无眼内炎症病例。两组的SRF和IRF体积均显著减少。在随访期间,两组患者的PED体积均显著减少(平均斜率= -206 nL, 95%CL = -273/-138;p值结论:12个月内,玻璃体内注射Faricimab可显著降低treatment-Naïve和无应答Switch患者的PED体积。该研究强调了Faricimab作为nAMD T1 MNV的有效治疗选择的潜力,提供了PED体积和相关液体生物标志物的显着改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Faricimab efficacy in type 1 macular neovascularization: AI-assisted quantification of pigment epithelium detachment (PED) volume reduction over 12 months in Naïve and switch eyes.

Background: This study evaluates the efficacy of intravitreal Faricimab in reducing pigment epithelium detachment (PED) and fluid volumes in both treatment-naïve eyes and eyes unresponsive to anti-VEGF mono-therapies, all diagnosed with type 1 macular neovascularization (T1 MNV) over a period of 12-month.

Methods: A retrospective, single-center cohort study was conducted at the Jules Gonin Eye Hospital, Lausanne, Switzerland. Clinical records of treatment-naïve and non-responder switch patients presenting T1 MNV secondary to neovascular age-related macular degeneration (nAMD) from September 2022 to March 2023 were reviewed. Patients received a loading dose of three monthly Faricimab injections followed by a treat-and-extend (T&E) regimen. Multimodal imaging, including structural OCT and AI-assisted analysis, was used to quantify PED volumes and related fluid biomarkers at baseline, 3-month, 6-month, and 12-month follow-up. Statistical analyses included linear mixed models to evaluate differences and trends in intraretinal (IRF), subretinal fluid (SRF) and PED volumes.

Results: 65 eyes of 65 patients were enrolled (female: 70.7%; mean age = 80.7yrs, SD = 6.9yrs). 80% had received anti-VEGF treatment (Switch group) and 20% were treatment-Naïve at baseline. At 12 months, intravitreal treatments were more frequent in the Switch group (mean number = 8.3 vs. 6.0; p = 0.009). BCVA improved at the 12-month follow-up in Naïve eyes (+ 6.9 ETDRS letters from baseline, p = 0.053) and was maintained in Switch eyes. No cases of intraocular inflammation were observed. Significant reduction in SRF and IRF volumes were noted in both groups. A significant reduction in PED volume was observed over the follow-up period in both groups (mean slope = -206 nL, 95%CL = -273/-138; p-value < 0.001).

Conclusions: Intravitreal Faricimab significantly reduced PED volumes in both treatment-Naïve and non-responder Switch patients over 12 months. The study highlights Faricimab's potential as an effective treatment option for T1 MNV in nAMD, offering significant improvements in PED volume and related fluid biomarkers.

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来源期刊
CiteScore
3.50
自引率
4.30%
发文量
81
审稿时长
19 weeks
期刊介绍: International Journal of Retina and Vitreous focuses on the ophthalmic subspecialty of vitreoretinal disorders. The journal presents original articles on new approaches to diagnosis, outcomes of clinical trials, innovations in pharmacological therapy and surgical techniques, as well as basic science advances that impact clinical practice. Topical areas include, but are not limited to: -Imaging of the retina, choroid and vitreous -Innovations in optical coherence tomography (OCT) -Small-gauge vitrectomy, retinal detachment, chromovitrectomy -Electroretinography (ERG), microperimetry, other functional tests -Intraocular tumors -Retinal pharmacotherapy & drug delivery -Diabetic retinopathy & other vascular diseases -Age-related macular degeneration (AMD) & other macular entities
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