Section of Ophthalmology, University of Calgary, Calgary, Alberta, Canada.
Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.
Surv Ophthalmol. 2022 Sep-Oct;67(5):1364-1372. doi: 10.1016/j.survophthal.2022.04.001. Epub 2022 Apr 19.
Refractory diabetic macular edema (DME) to monthly intravitreal anti-vascular endothelial growth factor (VEGF) monotherapy has a prevalence of approximately 40% in landmark clinical trials. Options for these patients include use of intravitreal steroids, focal laser, or switching to an alternative anti-VEGF agent. We summarize the key conclusions from studies analyzing the efficacy of switching anti-VEGF agents for refractory DME. Twenty-four studies were included in analysis. The most common definitions of refractory in the included studies were a central retinal thickness (CRT) greater than 300μm or a reduction in CRT less than 10% after at least 3-6 prior anti-VEGF injections. Switching to intravitreal aflibercept (IVA) from either intravitreal ranibizumab (IVR) or bevacizumab (IVB) is associated with moderate to significant improvement in central subfield thickness and may be an appropriate choice for patients with refractory DME. The improvement in retinal thickness and edema is typically seen after the first 3 injections of IVA post-switch. Switching to IVR has also demonstrated improvement in CRT at 3-6 months post switch in large sample population studies. Future studies are required to elucidate the ideal time point for a switch in anti-VEGF agent or which patients would benefit from this change.
在具有里程碑意义的临床试验中,每月接受玻璃体内抗血管内皮生长因子 (VEGF) 单一疗法治疗的难治性糖尿病黄斑水肿 (DME) 的患病率约为 40%。这些患者的治疗选择包括使用玻璃体内皮质类固醇、光凝或改用其他抗 VEGF 药物。我们总结了分析用于治疗难治性 DME 的抗 VEGF 药物转换疗效的研究的主要结论。共有 24 项研究纳入分析。纳入研究中难治性的最常见定义是中央视网膜厚度 (CRT) 大于 300μm 或在至少 3-6 次先前抗 VEGF 注射后 CRT 减少小于 10%。从玻璃体内雷珠单抗 (IVR) 或贝伐单抗 (IVB) 转换为玻璃体内阿柏西普 (IVA) 与 CRT 中央子区域厚度的中度至显著改善相关,对于难治性 DME 患者可能是一个合适的选择。在转换后的前 3 次 IVA 注射后,视网膜厚度和水肿的改善通常可见。在大型样本人群研究中,转换为 IVR 也证明在转换后 3-6 个月 CRT 有所改善。需要进一步的研究来阐明抗 VEGF 药物转换的理想时间点或哪些患者将从这种改变中受益。