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根据“治疗并延长”方案,比较抗血管生成药物(雷珠单抗、阿柏西普、贝伐单抗和Ziv-阿柏西普)对渗出型年龄相关性黄斑变性的治疗反应——真实的头对头研究。

Comparison of antiangiogenic agents (ranibizumab, aflibercept, bevacizumab and ziv-aflibercept) in the therapeutic response to the exudative form of age-related macular degeneration according to the treat-and-extend protocol- true head-to-head study.

作者信息

Kanadani Tereza, Rabelo Neiffer, Takahashi Denise, Magalhães Lucas, Farah Michel

机构信息

Retina Institute, Belo Horizonte, Brazil.

, Nova Lima, Brazil.

出版信息

Int J Retina Vitreous. 2024 Feb 2;10(1):13. doi: 10.1186/s40942-024-00537-5.

Abstract

PURPOSE

To evaluate the structural and functional changes in eyes with neovascular age related macular degeneration (nAMD) in a real-world setting, using Treat and Extend protocol (T&E), comparing four antiangiogenic agents.

METHODS

Prospective, observational, case series study performed in 131 patients with the exudative form of nAMD. Patients were randomly assigned into four groups according to the antiangiogenic agent. During the first year, all eyes received at least 3 monthly intravitreal injections of antiangiogenic agents, and afterwards, were submitted to the T&E.

RESULTS

There was statistically significant difference (p < 0.05) between pre- and post-treatment in the best corrected visual acuity measurements by drug used. Patients who used aflibercept had significantly fewer injections than patients using the other drugs (mean = 9.03). No significant difference was observed between the drugs bevacizumab, ranibizumab and ziv-aflibercept. With regard to biomarkers, patients who used aflibercept and had lower baseline central retinal thickness, absence of hyperreflective foci and no subretinal hyperreflective material had the lowest number of injections.

CONCLUSION

Results indicate that over 2 years, Intravitreal aflibercept on T&E provided better visual and anatomical improvements when compared to other drugs used in this study with significantly fewer injections.

摘要

目的

在真实世界环境中,使用治疗与延长方案(T&E)评估新生血管性年龄相关性黄斑变性(nAMD)患者眼睛的结构和功能变化,并比较四种抗血管生成药物。

方法

对131例渗出型nAMD患者进行前瞻性、观察性病例系列研究。根据抗血管生成药物将患者随机分为四组。在第一年,所有眼睛至少接受3次每月一次的玻璃体内抗血管生成药物注射,之后接受T&E方案。

结果

根据所用药物,治疗前后最佳矫正视力测量结果存在统计学显著差异(p < 0.05)。使用阿柏西普的患者注射次数明显少于使用其他药物的患者(平均 = 9.03次)。贝伐单抗、雷珠单抗和聚乙二醇化阿柏西普之间未观察到显著差异。关于生物标志物,使用阿柏西普且基线中心视网膜厚度较低、无高反射灶且无视网膜下高反射物质的患者注射次数最少。

结论

结果表明,在2年多的时间里,与本研究中使用的其他药物相比,采用T&E方案的玻璃体内注射阿柏西普在视力和解剖学改善方面效果更好,且注射次数显著减少。

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