Sydney Retina, Sydney, New South Wales, Australia.
Sydney Institute of Vision Science, Sydney, New South Wales, Australia.
Clin Exp Ophthalmol. 2020 Jan;48(1):53-60. doi: 10.1111/ceo.13636. Epub 2019 Oct 10.
To examine the effect of switching from intravitreal bevacizumab or ranibizumab to aflibercept in eyes with persistent macular oedema due to retinal vein occlusion (RVO).
We report the results of a prospective interventional study on the effect of aflibercept 2 mg in eyes with persistent macular oedema after long-term treatment with bevacizumab or ranibizumab.
Non-randomized, prospective clinical trial.
Eighteen eyes of eighteen patients were included.
Eyes with persistent macular oedema despite a minimum of four previous intravitreal bevacizumab/ranibizumab injections were recruited into this 48-week trial. Three loading doses of intravitreal aflibercept were administered every 4-weeks, thereafter every 8-weeks until week 48.
Mean change from baseline in best corrected visual acuity (BCVA) as measured by early treatment diabetic retinopathy score (ETDRS) and central macular thickness (CMT) as measured by spectral domain optical coherence tomography (SD-OCT) at 48 weeks.
Patients had received a mean of 40.0 ± 17.8 bevacizumab/ranibizumab intravitreal injections prior to switching to aflibercept. The mean number of previous injections administered in the 12-months preceding entry into the study was 10.2 ± 2.4. Mean vision change at week 48 was +21.1 ± 5.1 ETDRS letters in the BRVO group and +18.8 ± 5.9 letters at in the CRVO group (P < .001 for both groups). Mean decrease in CMT was 87.6 ± 48.8 μm and 191.0 ± 128.3 μm, in the BRVO and CRVO groups, respectively (P < .001). Using linear regression analyses, a higher number of previous intravitreal ranibizumab/bevacizumab injections and thicker pre-switch CMT were correlated with greater visual gains.
Switching to aflibercept from bevacizumab or ranibizumab in eyes with persistent macular oedema due to RVO can lead to functional and anatomical improvement. This effect was more obvious in eyes with a greater CMT prior to the switch.
目的:研究因视网膜静脉阻塞(RVO)导致的黄斑水肿持续存在的患者由玻璃体腔内注射贝伐单抗或雷珠单抗转换为阿柏西普的效果。
背景:我们报告了一项前瞻性干预研究的结果,该研究评估了在接受贝伐单抗或雷珠单抗长期治疗后,玻璃体腔内注射 2mg 阿柏西普对黄斑水肿持续存在的眼睛的影响。
设计:非随机、前瞻性临床试验。
参与者:纳入了 18 名患者的 18 只眼。
方法:纳入了在接受至少 4 次玻璃体腔内贝伐单抗/雷珠单抗注射后仍存在黄斑水肿的患者,这些患者参与了这项 48 周的试验。前 3 次玻璃体腔内注射阿柏西普为负荷剂量,每 4 周 1 次,之后每 8 周 1 次,直至第 48 周。
主要观察指标:在第 48 周时,使用早期糖尿病视网膜病变评分(ETDRS)测量的最佳矫正视力(BCVA)和光谱域光学相干断层扫描(SD-OCT)测量的中央黄斑厚度(CMT)的平均变化。
结果:在转换为阿柏西普之前,患者平均接受了 40.0±17.8 次贝伐单抗/雷珠单抗玻璃体腔内注射。在进入研究前的 12 个月内,平均接受的注射次数为 10.2±2.4 次。在 BRVO 组,第 48 周时视力变化的平均值为+21.1±5.1 ETDRS 字母,在 CRVO 组为+18.8±5.9 字母(两组均 P<.001)。BRVO 组和 CRVO 组的 CMT 平均下降分别为 87.6±48.8μm 和 191.0±128.3μm(P<.001)。线性回归分析显示,更多的玻璃体腔内雷珠单抗/贝伐单抗注射次数和转换前更厚的 CMT 与更好的视力改善相关。
结论和相关性:因 RVO 导致的黄斑水肿持续存在的患者由玻璃体腔内注射贝伐单抗或雷珠单抗转换为阿柏西普可导致功能和解剖学改善。在转换前 CMT 更大的眼中,这种效果更为明显。