Jaki Mekjavić Polona, Gregorčič Bogdan, Oberč Cvetka, Podgoršek Slava
Eye Hospital, University Medical Center Ljubljana, Grabloviceva 46, SI-1000, Ljubljana, Slovenia.
Medical Faculty, University of Ljubljana, Ljubljana, Slovenia.
BMC Ophthalmol. 2018 Dec 20;18(1):333. doi: 10.1186/s12886-018-1005-x.
To assess visual outcomes over 24 months in patients with neovascular age-related macular degeneration (nAMD) who initiated intravitreal aflibercept therapy under a treat-and-extend (TE) regimen in real-world settings.
In this retrospective, observational, multicentre study in Slovenia, medical records of all treatment-naïve patients with nAMD who started intravitreal aflibercept therapy between October 2013 and April 2015 were reviewed. The primary outcome measure was change in mean visual acuity (VA) from baseline to 24 months in patients who received the TE regimen for 2 years, assessed by standardised Early Treatment Diabetic Retinopathy Study charts and calculated as least-squares means. Other outcome measures included the numbers of injections and visits at 12 months and 24 months.
The primary analysis included 115 eyes of 105 patients who received TE treatment for 2 years (Group A). The mean VA improved from 57.9 ± 14.9 letters at baseline to 64.6 ± 15.8 letters (+ 6.5 letters, p < 0.0001) at 12 months and 64.8 ± 15.6 letters (+ 7.0 letters, p < 0.0001) at 24 months. The mean number of injections per eye was 8.4 ± 1.9 and the mean number of visits was 8.8 ± 1.7 at 12 months; these numbers decreased to 6.1 ± 2.0 and 6.4 ± 1.9, respectively, at 24 months. The additional analysis included 33 eyes of 33 patients who received TE treatment in Year 1, followed by pro re nata treatment in Year 2 (Group B). Compared with Group A whose vision improvement was maintained at 24 months, the VA gain in Group B eyes seen at 12 months (change in mean VA vs baseline: + 6.9 letters, p = 0.0008) was no longer present at 24 months (change in mean VA vs baseline: + 1.2 letters, p = 0.5733).
Using the TE regimen in clinical practice, intravitreal aflibercept significantly improved visual outcomes in treatment-naïve patients with nAMD, which were maintained over time. TE therapy with intravitreal aflibercept is a rational long-term strategy that can produce favourable outcomes in clinical practice.
评估在现实环境中接受玻璃体内阿柏西普治疗并采用治疗-延长(TE)方案的新生血管性年龄相关性黄斑变性(nAMD)患者24个月内的视力结果。
在斯洛文尼亚进行的这项回顾性、观察性、多中心研究中,对2013年10月至2015年4月期间开始接受玻璃体内阿柏西普治疗的所有初治nAMD患者的病历进行了回顾。主要结局指标是接受2年TE方案治疗的患者从基线到24个月时平均视力(VA)的变化,通过标准化的糖尿病视网膜病变早期治疗研究图表进行评估,并计算为最小二乘均值。其他结局指标包括12个月和24个月时的注射次数和就诊次数。
初步分析纳入了105例接受2年TE治疗的患者的115只眼(A组)。平均视力从基线时的57.9±14.9字母提高到12个月时的64.6±15.8字母(提高6.5字母,p<0.0001),24个月时为64.8±15.6字母(提高7.0字母,p<0.0001)。12个月时每只眼的平均注射次数为8.4±1.9次,平均就诊次数为8.8±1.7次;24个月时这些数字分别降至6.1±2.0次和6.4±1.9次。额外分析纳入了33例在第1年接受TE治疗、第2年按需治疗的患者的33只眼(B组)。与24个月时视力改善得以维持的A组相比,B组眼睛在12个月时的视力提高(平均视力相对于基线的变化:提高6.9字母,p=0.0008)在24个月时不再存在(平均视力相对于基线的变化:提高1.2字母,p=0.5733)。
在临床实践中使用TE方案,玻璃体内阿柏西普可显著改善初治nAMD患者的视力结果,且随着时间推移得以维持。玻璃体内阿柏西普的TE疗法是一种合理的长期策略,可在临床实践中产生良好的结果。