Resolution of Angiographic Macular Leakage with Faricimab versus Aflibercept in Patients with Diabetic Macular Edema in YOSEMITE/RHINE.

IF 4.4 Q1 OPHTHALMOLOGY Ophthalmology. Retina Pub Date : 2024-11-22 DOI:10.1016/j.oret.2024.11.015
Roger A Goldberg, Florie A Mar, Karl Csaky, Manuel Amador, Arshad M Khanani, Kara Gibson, Anton M Kolomeyer, Dawn A Sim, Toshinori Murata, Tracey Wang, Patricia Udaondo, Audrey Souverain, Yevgeniy Eugene Shildkrot, Stela Vujosevic, Eric Nudleman, Sobha Sivaprasad
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Abstract

Purpose: To evaluate if dual angiopoietin-2 (Ang-2)/VEGF-A inhibition with faricimab resulted in greater macular leakage resolution versus aflibercept in patients with diabetic macular edema (DME).

Design: Post hoc analysis of macular leakage assessments prespecified in the YOSEMITE/RHINE (NCT03622580/NCT03622593) phase III trials.

Participants: Adults with visual acuity loss due to center-involving DME.

Methods: Patients were randomized 1:1:1 to faricimab 6.0 mg every 8 weeks (Q8W), faricimab 6.0 mg according to a personalized treat-and-extend (T&E)-based regimen, or aflibercept 2.0 mg Q8W. This analysis included the first 16 weeks (head-to-head dosing period) when all patients received assigned study drug every 4 weeks (Q4W); patients were assessed 4 weeks after receiving 4 doses of assigned study drug Q4W.

Main outcome measures: Macular leakage area on fluorescein angiography assessed by a reading center; proportion of patients with resolution of macular leakage (defined as macular leakage area 0-1 mm2) and high macular leakage (defined as macular leakage area ≥10 mm2) at baseline and week 16; and the proportion of faricimab T&E patients receiving Q16W dosing at week 52 among those with resolution of and high macular leakage at week 16.

Results: Among patients with macular leakage data available at baseline, there were 1216 patients in the pooled faricimab (Q8W + T&E) arms and 593 patients in the aflibercept arm. Baseline median macular leakage area was similar between the faricimab (24.6 mm2) and aflibercept arms (25.6 mm2). At week 16, median macular leakage area was 3.6 mm2 with faricimab versus 7.6 mm2 with aflibercept (nominal P < 0.0001). More faricimab-treated patients (28%) achieved resolution of macular leakage versus aflibercept at week 16 (15%; nominal P < 0.0001). In the faricimab T&E arm, 63% of patients with resolution of macular leakage and 45% of patients with high macular leakage at week 16 achieved Q16W dosing at week 52 (nominal P < 0.01).

Conclusions: Faricimab demonstrated greater macular leakage resolution versus aflibercept during head-to-head dosing. These findings suggest that dual Ang-2/VEGF-A inhibition promotes vascular stability beyond VEGF inhibition alone, supporting faricimab's potential to offer greater disease control and extend durability for patients with DME.

Financial disclosure(s): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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在 YOSEMITE/RHINE 项目中,使用 Faricimab 与 Aflibercept 治疗糖尿病黄斑水肿患者的血管造影黄斑渗漏。
目的:评估使用法尼单抗抑制血管生成素-2(Ang-2)/血管内皮生长因子-A(VEGF-A)是否能比阿夫利拜因更有效地解决糖尿病黄斑水肿(DME)患者的黄斑渗漏问题.设计:对YOSEMITE/RHINE(NCT03622580/NCT03622593)3期试验中预设的黄斑渗漏评估进行事后分析:设计:对YOSEMITE/RHINE(NCT03622580/NCT03622593)3期试验中预设的黄斑渗漏评估进行事后分析:方法:患者按1:1:1随机分配至法尼单抗6.0毫克,每8周一次(Q8W);法尼单抗6.0毫克,根据个性化治疗和延长方案(T&E);或阿弗利百普2.0毫克,每8周一次(Q8W)。该分析包括所有患者接受指定研究药物Q4W的前16周(头对头给药期);患者在接受4次指定研究药物Q4W给药后4周接受评估:由阅片中心评估荧光素血管造影的黄斑渗漏面积;基线和第16周黄斑渗漏缓解(定义为黄斑渗漏面积为0-1平方毫米)和黄斑渗漏严重(定义为黄斑渗漏面积≥10平方毫米)的患者比例;第16周黄斑渗漏缓解和黄斑渗漏严重的患者中,第52周接受Q16W给药的法尼单抗T&E患者比例:在基线时有黄斑渗漏数据的患者中,共有1216名患者接受了法尼单抗(Q8W + T&E)治疗,593名患者接受了阿夫利百普治疗。法尼单抗组(24.6 平方毫米)和阿弗利百普组(25.6 平方毫米)的基线中位黄斑渗漏面积相似。第16周时,法尼单抗治疗组的黄斑中位渗漏面积为3.6平方毫米,而阿夫利韦齐治疗组为7.6平方毫米(名义P < 0.0001)。与阿弗利百普相比,更多的法尼单抗治疗患者(28%)在第16周解决了黄斑渗漏问题(15%;名义 P < 0.0001)。在法尼单抗T&E治疗组中,第16周黄斑渗漏缓解的患者中有63%、黄斑渗漏严重的患者中有45%在第52周达到了Q16W剂量(名义P < 0.01):结论:在头对头用药期间,法利单抗的黄斑渗漏缓解率高于阿夫利百普。这些研究结果表明,Ang-2/VEGF-A双重抑制对血管稳定性的促进作用超过了单纯的VEGF抑制,这支持了法利单抗为DME患者提供更强的疾病控制和延长耐久性的潜力。
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来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
期刊最新文献
Follow-up Algorithm after Bevacizumab Treatment for Retinopathy of Prematurity. Low Dose Bevacizumab 0.03 mg for Treatment of Type I Retinopathy of Prematurity. Re: Muayad et al.: Influence of common medications on diabetic macular edema in type 2 diabetes mellitus (Ophthalmol Retina. 2024 Dec 5:S2468-6530(24)00582-7. doi: 10.1016/j.oret.2024.12.006. Online ahead of print.). Reply. Retinal Vessel Printings in Retinal Pigment Epithelium Exposure.
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