Trauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.
Chair and Clinical Department of Ophthalmology, Division of Medical Science in Zabrze, Medical University of Silesia in Katowice, 40-760 Katowice, Poland.
Int J Environ Res Public Health. 2022 Feb 17;19(4):2303. doi: 10.3390/ijerph19042303.
Age-related macular degeneration (AMD) is a progressive, chronic disease of the central area of the retina, which, if untreated, leads to blindness. This study aimed to compare the effectiveness of therapy using anti-VEGF drugs, namely brolucizumab and aflibercept, in patients with neovascular AMD (nAMD) during a monitoring period lasting around 20 weeks. The analysis consisted of 40 patients diagnosed with neovascular age-related macular degeneration, with 20 patients receiving aflibercept (Eylea, Bayer) at a dose of 2 mg/50 µL into the vitreous chamber at the following intervals-3 doses, 4 weeks apart, followed by a fourth dose after 8 weeks. The remaining 20 patients received brolucizumab (Beovu, Novartis) at a dose of 6 mg/50 µL, administered in the following schedule-3 initial doses, 4 weeks apart, with the administration of a fourth dose decided for each patient individually by the doctor, depending on disease activity, assessed through imaging tests. To evaluate treatment effectiveness, the following measurements were used: 'read distance and near visual acuity' for each eye separately using the Snellen chart; and non-invasive retinal imaging techniques-optical coherence tomography (OCT) and OCT angiography (OCTA). In patients treated using brolucizumab, during the observation period, statistically significant differences were found in the following parameters: flow area ( = 0.0277); select area ( = 0.0277); FOVEA ( = 0.0073); visus ( = 0.0064). In brolucizumab-treated patients, changes in OCT and OCTA, indicating an improvement, were already visible after the first injection of the drug, whereas in the aflibercept-treated group, changes were only visible after the fourth injection. We found a higher effectiveness of brolucizumab therapy compared to aflibercept in patients with nAMD during an observations period lasting 20 weeks. Our observations are significant, although they require further research.
年龄相关性黄斑变性(AMD)是一种进行性、慢性的视网膜中央区域疾病,如果不治疗,会导致失明。本研究旨在比较在大约 20 周的监测期间使用抗血管内皮生长因子(VEGF)药物,即 brolucizumab 和 aflibercept,治疗新生血管性 AMD(nAMD)患者的疗效。分析包括 40 名被诊断为新生血管性年龄相关性黄斑变性的患者,其中 20 名患者接受 aflibercept(Eylea,拜耳)玻璃体腔注射,剂量为 2 mg/50 μL,间隔 4 周注射 3 次,然后在 8 周后再注射第 4 次。其余 20 名患者接受 brolucizumab(Beovu,诺华)玻璃体腔注射,剂量为 6 mg/50 μL,按以下方案给药:3 次初始剂量,间隔 4 周,根据疾病活动度,由医生单独为每位患者决定是否给予第 4 次注射,通过影像学检查评估。为了评估治疗效果,使用以下测量方法:使用 Snellen 图表分别测量每只眼睛的“远视力和近视力”;以及非侵入性视网膜成像技术——光学相干断层扫描(OCT)和 OCT 血管造影术(OCTA)。接受 brolucizumab 治疗的患者在观察期间,以下参数存在统计学显著差异:血流面积( = 0.0277);选择面积( = 0.0277);FOVEA( = 0.0073);视力( = 0.0064)。在接受 brolucizumab 治疗的患者中,药物首次注射后,OCT 和 OCTA 就已经显示出改善的迹象,而在 aflibercept 治疗组中,只有在第 4 次注射后才显示出变化。我们发现,在 20 周的观察期间,与 aflibercept 相比,brolucizumab 治疗 nAMD 的效果更高。我们的观察结果很有意义,尽管还需要进一步的研究。