Zhou Pengyi, Yang Lin, Jin Xuemin
Department of Ophthalmology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, He'nan - China.
Eur J Ophthalmol. 2016 May-Jun;26(3):262-7. doi: 10.5301/ejo.5000691. Epub 2015 Oct 14.
To compare the efficacy and safety of bevacizumab vs ranibizumab for the treatment of idiopathic choroidal neovascularization (ICNV).
This retrospective study included 60 eyes of 60 patients with ICNV who underwent intravitreal injection of bevacizumab (1.25 mg/0.05 mL, n = 30 eyes) or ranibizumab (0.5 mg/0.05 mL, n = 30 eyes). Multiple treatments were based on complete ophthalmologic investigation including slit-lamp biomicroscopy, fundus examination, fundus fluorescein angiography (FFA), optical coherence tomography (OCT), and best-corrected visual acuity (BCVA). The BCVA, central retinal thickness (CRT), intraocular pressure (IOP), FFA results, and complications were compared between the 2 groups during the 2-year follow-up.
Visual acuity was significantly better at 1, 3, 6, 12, and 24 months after treatment (p<0.01), with no significant difference in visual acuity between the bevacizumab and ranibizumab groups. In both groups of patients, the CRT after treatment was significantly less than before. At 12 and 24 months, the CRT in the ranibizumab group was significantly less than in the bevacizumab group (p<0.05). The FFA examination showed that CNV was reduced after intravitreal injection of either drug, with no significant difference in IOP between the 2 groups. No ophthalmologic or systemic complications occurred.
Bevacizumab and ranibizumab are effective and safe in the treatment of ICNV, with similar effects in improving visual acuity and reducing retinal edema. The long-term efficacy of ranibizumab is superior to bevacizumab in reducing CRT.
比较贝伐单抗与雷珠单抗治疗特发性脉络膜新生血管(ICNV)的疗效和安全性。
这项回顾性研究纳入了60例ICNV患者的60只眼,这些患者接受了玻璃体腔内注射贝伐单抗(1.25 mg/0.05 mL,n = 30只眼)或雷珠单抗(0.5 mg/0.05 mL,n = 30只眼)。多次治疗基于全面的眼科检查,包括裂隙灯生物显微镜检查、眼底检查、眼底荧光血管造影(FFA)、光学相干断层扫描(OCT)和最佳矫正视力(BCVA)。在2年的随访期间,比较两组之间的BCVA、中心视网膜厚度(CRT)、眼压(IOP)、FFA结果和并发症。
治疗后1、3、6、12和24个月时视力明显改善(p<0.01),贝伐单抗组和雷珠单抗组之间的视力无显著差异。两组患者治疗后的CRT均明显低于治疗前。在12个月和24个月时,雷珠单抗组的CRT明显低于贝伐单抗组(p<0.05)。FFA检查显示,玻璃体腔内注射任何一种药物后CNV均减少,两组之间的IOP无显著差异。未发生眼科或全身并发症。
贝伐单抗和雷珠单抗治疗ICNV有效且安全,在提高视力和减轻视网膜水肿方面效果相似。雷珠单抗在降低CRT方面的长期疗效优于贝伐单抗。