Network Meta-Analysis of Bevacizumab Gamma Versus Competing Interventions for Treating Neovascular Age-Related Macular Degeneration in the United Kingdom.
Maria Lorenzi, Stephen Ebohon, Jennifer Kissner, Jedd Comiskey, Mayke Paap, Christine Bouchet, Andy Garnham, Erika Wissinger
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引用次数: 0
Abstract
This study aimed to determine the relative efficacy of bevacizumab gamma (an ophthalmic formulation of bevacizumab) versus alternative interventions relevant to the treatment of neovascular age-related macular degeneration (nAMD) in the United Kingdom (UK) via a systematic literature review (SLR) and network meta-analysis (NMA). An SLR was conducted to identify randomized controlled trials (RCTs) of anti-vascular endothelial growth factor (anti-VEGF) therapies for the treatment of nAMD in adult patients relevant to the UK context. The included anti-VEGF treatments were ranibizumab, aflibercept, faricimab, and bevacizumab gamma. Bayesian NMA models were used to estimate relative efficacy in terms of change from baseline (CFB) in best-corrected visual acuity (BCVA) at 12 months, the proportion of patients gaining 15 or more letters at 12 months, and the proportion of patients losing less than 15 letters at 12 months. Twenty-two relevant RCTs were included in the NMA. At 12 months, all anti-VEGF treatments were similarly efficacious to ranibizumab 0.5 mg every four weeks (Q4W) in terms of CFB in BCVA, the proportion of patients gaining 15 or more letters, and the proportion of patients losing less than 15 letters (except for ranibizumab 0.5 mg every 12 weeks [Q12W] and ranibizumab 0.5 mg pro re nata [PRN]). Bevacizumab gamma provided similar improvements in visual acuity to other anti-VEGF treatments.
本研究旨在通过系统文献综述(SLR)和网络荟萃分析(NMA),确定贝伐单抗γ(贝伐单抗的眼科配方)与英国(UK)治疗新生血管性年龄相关性黄斑变性(nAMD)相关的替代干预措施的相对疗效。我们进行了一项SLR,以确定与英国相关的成人患者中抗血管内皮生长因子(anti-VEGF)治疗nAMD的随机对照试验(rct)。纳入的抗vegf治疗包括雷尼单抗、阿非利塞普、法利西单抗和贝伐单抗。使用贝叶斯NMA模型来估计12个月时最佳矫正视力(BCVA)的基线变化(CFB)的相对疗效,12个月时获得15个或更多字母的患者比例,以及12个月时失去小于15个字母的患者比例。NMA纳入了22项相关rct。在12个月时,所有抗vegf治疗在BCVA的CFB、获得15个或更多字母的患者比例以及损失小于15个字母的患者比例方面均与兰尼单抗0.5 mg / 4周(Q4W)相似(除了兰尼单抗0.5 mg / 12周[Q12W]和兰尼单抗0.5 mg pro re nata [PRN])。与其他抗vegf治疗相比,贝伐单抗提供了类似的视力改善。