Department of Ophthalmology, Glostrup Hospital, Glostrup, Denmark University of Copenhagen, Copenhagen, Denmark.
Acta Ophthalmol. 2013 Feb;91(1):42-7. doi: 10.1111/j.1755-3768.2011.02268.x. Epub 2011 Oct 19.
To describe predictors of visual outcome in patients treated with intravitreal ranibizumab for choroidal neovascularisation (CNV) in age-related macular degeneration (AMD).
Retrospective review of 279 patients with CNV in AMD who fulfilled MARINA/ANCHOR study eligibility criteria and were treated with repeated intravitreal injections of ranibizumab 0.5 mg in routine clinical practice, beginning with three initial injections at 4-week intervals followed by individualized retreatment for the subsequent 9 months. Study parameters included best-corrected visual acuity (BCVA) and morphological characteristics.
Mean BCVA relative to baseline was +4.7 (p < 0.0001), +4.2 (p < 0.0001)and -0.4 (p > 0.667) Early Treatment Diabetic Retinopathy Study letters after 3, 6 and 12 months, respectively, after a mean of 5.1 injections when the proportion of patients with BCVA ≥ 70 letters had doubled compared with baseline. Predictive factors for BCVA ≤ 35 letters after 12 months were BCVA ≤ 35 letters at baseline and month 3 (p < 0.0001) while BCVA ≥ 70 letters at month 12 was associated with BCVA ≥ 70 letters at baseline and month 3 (p < 0.001) and with total lesion size <4 DA (p = 0.0147).
Under a ranibizumab regimen with substantially fewer injections than with fixed four-weekly injection regimens, BCVA was improved compared with the natural history of neovascular AMD, but did not achieve the visual gain observed in randomized clinical trials using fixed 4-week retreatment. Visual acuity at month 3, after the initial fixed-interval injections, was the strongest predictor of BCVA at month 12.
描述接受玻璃体内雷珠单抗治疗年龄相关性黄斑变性(AMD)脉络膜新生血管(CNV)患者的视力结果预测因素。
对 279 例符合 MARINA/ANCHOR 研究入选标准并接受玻璃体内雷珠单抗 0.5mg 重复注射治疗的 AMD 合并 CNV 患者进行回顾性分析,这些患者在常规临床实践中接受治疗,最初每 4 周注射 3 次,随后在接下来的 9 个月内根据个体情况进行重复治疗。研究参数包括最佳矫正视力(BCVA)和形态学特征。
与基线相比,3、6 和 12 个月时的平均 BCVA 分别增加了+4.7(p<0.0001)、+4.2(p<0.0001)和-0.4(p>0.667)ETDRS 字母,在平均注射 5.1 次后,BCVA≥70 字母的患者比例是基线时的两倍。12 个月时 BCVA≤35 字母的预测因素是基线和第 3 个月时 BCVA≤35 字母(p<0.0001),而第 12 个月时 BCVA≥70 字母与基线和第 3 个月时 BCVA≥70 字母(p<0.001)和总病变面积<4 DA(p=0.0147)有关。
在雷珠单抗治疗方案下,与固定的每 4 周注射方案相比,注射次数显著减少,与新生血管性 AMD 的自然病程相比,BCVA 得到了改善,但与使用固定 4 周重复治疗的随机临床试验中观察到的视力增益不同。最初固定间隔注射后第 3 个月的视力是第 12 个月时 BCVA 的最强预测因素。