Medical Retina Department, Leicester Royal Infirmary, University Hospitals of Leicester, Leicester, UK.
1st Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Adv Ther. 2019 Jul;36(7):1532-1548. doi: 10.1007/s12325-019-00971-0. Epub 2019 May 17.
Emerging anti-vascular endothelial growth factor (anti-VEGF) therapies for neovascular age-related macular degeneration (nAMD) have revolutionised medical retina practice and the management and eventual outcome of nAMD. Recent research has focused on evaluating and comparing the efficacy of the two most widely employed anti-VEGF agents, bevacizumab and ranibizumab; however, a subgroup of patients with nAMD demonstrates a suboptimal response to standard therapy. We have therefore conducted a review of pertinent studies published until August 2018 which have documented the clinical efficacy when switching to a different anti-VEGF. Evidence on baseline disease characteristics, injection frequency and disease outcome has been obtained for patients treated with ranibizumab 0.5 mg and/or bevacizumab 1.25 mg and were switched to aflibercept 2 mg. Our review identified 45 studies investigating switching to aflibercept. Our review showed a clear anatomical benefit after the switch in terms of central retinal thickness and pigment epithelium detachment characteristics, whereas the functional outcomes were variable. Remarkable heterogeneity was documented among the relevant studies with regard to several factors including the baseline characteristics of the cohorts, the non-response definition and previous treatment protocols. Larger prospective trials with appropriate control arms are therefore required to elucidate the potential benefit when switching between anti-VEGF agents in refractory nAMD.
新兴的抗血管内皮生长因子(抗-VEGF)疗法治疗新生血管性年龄相关性黄斑变性(nAMD)彻底改变了医学视网膜学实践以及 nAMD 的管理和最终结果。最近的研究集中在评估和比较两种应用最广泛的抗-VEGF 药物,贝伐单抗和雷珠单抗的疗效上;然而,nAMD 的亚组患者对标准治疗的反应并不理想。因此,我们对截至 2018 年 8 月发表的相关研究进行了综述,这些研究记录了改用不同的抗-VEGF 药物的临床疗效。对接受雷珠单抗 0.5mg 和/或贝伐单抗 1.25mg 治疗且改用阿柏西普 2mg 的患者的基线疾病特征、注射频率和疾病结局进行了证据收集。我们的综述共纳入了 45 项研究,这些研究均涉及改用阿柏西普。我们的综述表明,在改用阿柏西普后,在解剖学上有明确的获益,表现在中心视网膜厚度和色素上皮脱离特征方面,而在功能结局方面则存在差异。与多项因素有关,包括队列的基线特征、无应答定义和之前的治疗方案,相关研究存在显著的异质性。因此,需要开展更大规模的前瞻性试验,并设立适当的对照组,以阐明在难治性 nAMD 中改用抗-VEGF 药物的潜在获益。