The first experience with brolucizumab for neovascular age-related macular degeneration

Q4 Medicine
A. Kulikov, D. Maltsev, A. Malafeeva, S.M. Perminova, V. R. Zhalimova, A. Vasiliev, A. Kazak
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引用次数: 4

Abstract

Aim: to assess the efficacy and safety of brolucizumab in Russian patients with neovascular age-related macular degeneration (nAMD). Patients and Methods: this study enrolled 47 patients with nAMD divided into two groups. Group 1 included 13 treatment-naïve patients/13 eyes (12 men and 1 woman, mean age 72.4±9.5 years, mean best-corrected visual acuity (BCVA) 0.43±0.32). Group 2 included 34 patients having active nAMD despite ongoing treatment/34 eyes (25 men and 9 women, mean age 74.1±8.0 years, mean BCVA 0.46±0.25). All patients received at least two intravitreal injections of brolucizumab (in total, 137 injections) with a 1-month interval. Patients were examined one month after the 2nd injections. BCVA, central macular thickness (CMT), macular volume (MV), sub/intraretinal fluid, and adverse events were evaluated. Results: in group 1, a significant increase in BCVA from 34.9±6.6 letters to 44.1±4.2 letters (p=0.02) was reported. Meanwhile, in group 2, BCVA remained unchanged (35.0±3.5 letters before treatment vs. 33.8±3.7 letters after treatment, p>0.05). In group 1, CMT and MV significantly reduced, while in group 2, only MV significantly reduced (p<0.05). A significant reduction in the cumulative rate of sub/ intraretinal fluid was detected in both groups (p<0.05). Conclusions: treatment-naïve patients who received brolucizumab demonstrated a significant improvement of anatomical and functional parameters. Meanwhile, patients with active nAMD despite ongoing treatment who received brolucizumab demonstrated a significant reduction in disease activity and tendency to the improvement of anatomical (but not functional) parameters. Keywords: age-related macular degeneration, brolucizumab, optical coherence tomography, anti-VEGF therapy. For citation: Kulikov A.N., Maltsev D.S., Malafeeva A.Yu. et al. The first experience with brolucizumab for neovascular age-related macular degeneration. Russian Journal of Clinical Ophthalmology. 2022;22(2):108–115 (in Russ.). DOI: 10.32364/2311-7729-2022-22-2-108-115.
布卢珠单抗治疗新生血管性年龄相关性黄斑变性的首次经验
目的:评估brolucizumab在俄罗斯新生血管性年龄相关性黄斑变性(nAMD)患者中的疗效和安全性。患者和方法:本研究纳入47例nAMD患者,分为两组。1组13例treatment-naïve患者/13只眼(男12女1),平均年龄72.4±9.5岁,平均最佳矫正视力(BCVA) 0.43±0.32。组2包括34例持续治疗仍有活动性nAMD的患者/34只眼(男性25例,女性9例,平均年龄74.1±8.0岁,平均BCVA 0.46±0.25)。所有患者接受至少2次玻璃体内注射brolucizumab(共137次注射),间隔1个月。第二次注射后1个月复查。评估BCVA、黄斑中心厚度(CMT)、黄斑体积(MV)、视网膜下/视网膜内液体和不良事件。结果:1组BCVA由34.9±6.6个字母显著增加至44.1±4.2个字母(p=0.02)。同时,2组BCVA无变化(治疗前为35.0±3.5个字母,治疗后为33.8±3.7个字母,p>0.05)。1组CMT和MV显著降低,2组仅MV显著降低(p<0.05)。两组患者视网膜下/腔内积液率均显著降低(p<0.05)。结论:treatment-naïve接受brolucizumab治疗的患者显示出解剖和功能参数的显著改善。与此同时,接受brolucizumab治疗的活动性nAMD患者显示出疾病活动性显著降低和解剖(但不是功能)参数改善的趋势。关键词:年龄相关性黄斑变性,brolucizumab,光学相干断层扫描,抗vegf治疗。引证:Kulikov A.N, Maltsev D.S, Malafeeva a.u u。et al。布卢珠单抗治疗新生血管性年龄相关性黄斑变性的首次经验。俄罗斯临床眼科杂志。2022;22(2):108-115(俄文)。DOI: 10.32364 / 2311-7729-2022-22-2-108-115。
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
CiteScore
0.60
自引率
0.00%
发文量
21
审稿时长
20 weeks
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