Department of Retina, Ophthalmic Consultants of Boston, Boston, Massachusetts 02114, USA.
Br J Ophthalmol. 2013 Aug;97(8):1032-5. doi: 10.1136/bjophthalmol-2013-303344. Epub 2013 Jun 13.
To investigate the effect of aflibercept 2.0 mg in cases resistant to ranibizumab 0.5 mg and/or bevacizumab 1.25 mg treatment.
To evaluate the anatomic and visual effect of intravitreal aflibercept 2.0 mg in cases of exudative age-related macular degeneration (AMD) with persistent fluid on optical coherence tomography (OCT) despite regular ranibizumab 0.5 mg and/or bevacizumab 1.25 mg treatment at 1 and 6 months.
Retrospective review at Ophthalmic Consultants of Boston, Boston, Massachusetts, USA of exudative AMD cases with persistent fluid on regular ranibizumab 0.5 mg and/or bevacizumab 1.25 mg treatment switched to intravitreal aflibercept 2.0 mg treatment and followed for 6 months. Tabulated data included details of prior treatments, best available visual acuity, central subfoveal thickness on registered spectral domain OCT before and after aflibercept injection centred on the anatomic fovea and macular description before and after aflibercept injection.
A total of 353 eyes with exudative AMD were switched to aflibercept during the study period. Of these, 28 eyes in 28 patients had persistent fluid after an average of 20 regular ranibizumab/bevacizumab injections (range 7-37). At 1 month, 89% (25 eyes) showed anatomic improvement and 18% (five eyes) were dry after a single aflibercept injection. Central subfoveal thickness improved from 295 to 272 microns (p<0.001) after one aflibercept injection. After an average of 4.4 aflibercept injections (range 3-6) over 6 months, the central subfoveal thickness remained improved (274 microns, p=0.008); 64% (18 eyes) showed anatomic improvement and a quarter of eyes (25%, seven eyes) were dry. Visual acuity did not improve at 1 month (logarithm of minimum angle of resolution (logMAR) 0.54, Snellen 20/69, p=0.64) or 6 months (logMAR 0.57, Snellen 20/76, p=0.49). Treatment was well tolerated with no adverse events reported.
A significant proportion of exudative AMD cases with persistent fluid on OCT despite regular ranibizumab 0.5 mg and/or bevacizumab 1.25 mg treatment respond anatomically to aflibercept 2.0 mg. Visual acuity did not improve. Aflibercept may be beneficial anatomically in cases of exudative AMD treated with persistent fluid on ranibizumab and/or bevacizumab.
探讨阿柏西普 2.0mg 治疗对雷珠单抗 0.5mg 和/或贝伐单抗 1.25mg 治疗抵抗病例的疗效。
评估玻璃体内注射阿柏西普 2.0mg 对持续性眼内液的渗出性年龄相关性黄斑变性(AMD)的解剖和视觉效果,这些患者在接受雷珠单抗 0.5mg 和/或贝伐单抗 1.25mg 治疗 1 个月和 6 个月后,光学相干断层扫描(OCT)显示仍有持续性眼内液。
美国马萨诸塞州波士顿眼科顾问公司对在接受雷珠单抗 0.5mg 和/或贝伐单抗 1.25mg 治疗后仍有持续性眼内液的渗出性 AMD 病例进行回顾性分析,这些病例已转为玻璃体内注射阿柏西普 2.0mg 治疗,并随访 6 个月。列出的数据包括先前治疗的详细信息、最佳可用视力、阿柏西普注射前和注射后以解剖中心凹为中心的黄斑中心凹下中心视网膜厚度(在黄斑区描述之前和之后)。
在研究期间,共有 353 只患有渗出性 AMD 的眼睛转为阿柏西普治疗。其中,28 例(28 只眼)在平均接受 20 次雷珠单抗/贝伐单抗治疗后仍有持续性眼内液(7-37 次)。在第 1 个月,89%(25 只眼)在单次阿柏西普注射后出现解剖学改善,18%(5 只眼)眼内液干涸。单次阿柏西普注射后,黄斑中心凹下中心视网膜厚度从 295μm 改善至 272μm(p<0.001)。在 6 个月内平均接受 4.4 次阿柏西普注射(3-6 次)后,黄斑中心凹下中心视网膜厚度仍有改善(274μm,p=0.008);64%(18 只眼)出现解剖学改善,四分之一的眼(25%,7 只眼)眼内液干涸。第 1 个月和第 6 个月的视力均无改善(最小分辨角对数视力(logMAR)0.54,Snellen 20/69,p=0.64;logMAR 0.57,Snellen 20/76,p=0.49)。治疗耐受性良好,无不良反应报告。
尽管接受雷珠单抗 0.5mg 和/或贝伐单抗 1.25mg 治疗,但 OCT 显示仍有持续性眼内液的渗出性 AMD 病例中,相当一部分对阿柏西普 2.0mg 有解剖学反应。视力没有提高。阿柏西普可能对接受雷珠单抗和/或贝伐单抗治疗并伴有持续性眼内液的渗出性 AMD 病例具有解剖学益处。