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雷珠单抗1+按需给药方案与贝伐单抗在临床环境中的对比研究。

Comparative study of 1+PRN ranibizumab versus bevacizumab in the clinical setting.

作者信息

Carneiro Angela M, Mendonça Luis S, Falcão Manuel S, Fonseca Sofia L, Brandão Elisete M, Falcão-Reis Fernando M

机构信息

Department of Ophthalmology of Hospital de São João, Porto, Portugal.

出版信息

Clin Ophthalmol. 2012;6:1149-57. doi: 10.2147/OPTH.S33017. Epub 2012 Jul 19.

Abstract

PURPOSE

We compared the efficacy of intravitreal ranibizumab and bevacizumab for treating neovascular age-related macular degeneration using an on-demand regimen.

METHODS

A total of 186 wet age-related macular degeneration eyes of 186 treatment-naïve patients were compared retrospectively (67 eyes treated with ranibizumab with 91 treated with bevacizumab). At baseline, mean age, best corrected visual acuity, and angiographic lesion types were similar in both groups. Best corrected visual acuity and ocular coherence tomography were evaluated.

RESULTS

Sixty eyes treated with ranibizumab and 85 eyes treated with bevacizumab completed a 12-month evaluation. At 12 months, mean best corrected visual acuity increased by +6.65 letters with ranibizumab treatment and by +5.59 with bevacizumab treatment (P = 0.64). Visual acuity improved by ≥15 letters in 15 eyes treated with ranibizumab and in 21 eyes treated with bevacizumab (P = 0.75). An overall reduction in ocular coherence tomography central thickness occurred for all time points. The mean number of injections per eye was 5.97 with ranibizumab and 5.92 with bevacizumab (P = 0.90).

CONCLUSION

Intravitreal therapies with ranibizumab or bevacizumab have similar visual and anatomical results. These results confirm those of comparison of Age-Related Macular Degeneration Treatment Trials in as-needed cohorts in clinical practice. Randomized long-term clinical trials are necessary to examine the systemic safety of these treatments.

摘要

目的

我们比较了玻璃体内注射雷珠单抗和贝伐单抗按需给药方案治疗新生血管性年龄相关性黄斑变性的疗效。

方法

回顾性比较186例初治患者的186只湿性年龄相关性黄斑变性眼(67只眼接受雷珠单抗治疗,91只眼接受贝伐单抗治疗)。基线时,两组的平均年龄、最佳矫正视力和血管造影病变类型相似。评估最佳矫正视力和光学相干断层扫描。

结果

60只接受雷珠单抗治疗的眼和85只接受贝伐单抗治疗的眼完成了12个月的评估。12个月时,雷珠单抗治疗组的平均最佳矫正视力提高了+6.65字母,贝伐单抗治疗组提高了+5.59字母(P = 0.64)。15只接受雷珠单抗治疗的眼和21只接受贝伐单抗治疗的眼视力提高≥15字母(P = 0.75)。所有时间点光学相干断层扫描中心厚度均出现总体下降。雷珠单抗治疗组每只眼的平均注射次数为5.97次,贝伐单抗治疗组为5.92次(P = 0.90)。

结论

玻璃体内注射雷珠单抗或贝伐单抗治疗具有相似的视力和解剖学结果。这些结果证实了年龄相关性黄斑变性治疗试验在临床实践中按需队列比较的结果。需要进行随机长期临床试验来检验这些治疗的全身安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c4/3422156/d1f207d9d8b0/opth-6-1149f1.jpg

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