B. B. Eye Foundation, 2/5, Sarat Bose Road, Kolkata - 700 020, India.
Indian J Ophthalmol. 2011 May-Jun;59(3):191-6. doi: 10.4103/0301-4738.81023.
Ranibizumab and bevacizumab are used widely for treating patients with choroidal neovascular membrane (CNVM) secondary to age-related macular degeneration (AMD).
To determine and compare the efficacy and safety of intravitreal ranibizumab and bevacizumab in treatment of CNVM due to AMD.
Prospective comparative case series carried out in an eye institute and eye department of a hospital in Kolkata, India.
One hundred and four eyes with CNVM due to AMD were randomized into two groups. Group A (n=54; 24 occult) received monthly intravitreal ranibizumab injections (0.5 mg in 0.05 ml) and Group B (n=50; 22 occult) received monthly bevacizumab injections (1.25 mg in 0.05 ml) for 3 consecutive months and then as per study criteria. Data analysis done using SPSS software. P-value of <0.05 was considered statistically significant.
The mean best corrected visual acuity (BCVA) in the ranibizumab group increased from 58.19 Early Treatment Diabetic Retinopathy Study (ETDRS) letters at baseline to 64 ETDRS letters at month 3 (P<0.001). In bevacizumab group mean BCVA increased from 56.80 to 61.72 ETDRS letters at month 3 (P<0.001). At the end of 18 months, there was no statistically significant difference between groups A and B with respect to change in BCVA (P=0.563) or central macular thickness (CMT; P=0.281), as measured by optical coherence tomography (Stratus OCT 3000). No significant sight-threatening complications developed.
Ranibizumab and bevacizumab are equally safe and efficacious in treating CNVM due to AMD.
雷珠单抗和贝伐单抗被广泛用于治疗年龄相关性黄斑变性(AMD)引起的脉络膜新生血管膜(CNVM)患者。
确定并比较玻璃体内雷珠单抗和贝伐单抗治疗 AMD 引起的 CNVM 的疗效和安全性。
在印度加尔各答的一家眼科研究所和医院的眼科部门进行的前瞻性对照病例系列研究。
104 只患有 AMD 引起的 CNVM 的眼睛被随机分为两组。A 组(n=54;24 例隐匿性)每月接受玻璃体内雷珠单抗注射(0.5mg 于 0.05ml),B 组(n=50;22 例隐匿性)每月接受玻璃体内贝伐单抗注射(1.25mg 于 0.05ml),连续 3 个月,然后根据研究标准进行注射。使用 SPSS 软件进行数据分析。P 值<0.05 被认为具有统计学意义。
雷珠单抗组的平均最佳矫正视力(BCVA)从基线时的 58.19 个早期治疗糖尿病视网膜病变研究(ETDRS)字母增加到第 3 个月时的 64 个 ETDRS 字母(P<0.001)。贝伐单抗组的平均 BCVA 从 56.80 增加到第 3 个月时的 61.72 ETDRS 字母(P<0.001)。在 18 个月结束时,A 组和 B 组在 BCVA 变化(P=0.563)或中央黄斑厚度(CMT;P=0.281)方面没有统计学意义的差异,这是通过光学相干断层扫描(Stratus OCT 3000)测量的。没有发生明显威胁视力的并发症。
雷珠单抗和贝伐单抗在治疗 AMD 引起的 CNVM 方面同样安全有效。