Network Meta-Analysis of Bevacizumab Gamma Versus Competing Interventions for Treating Neovascular Age-Related Macular Degeneration in the United Kingdom.

Q2 Medicine
Journal of market access & health policy Pub Date : 2025-11-19 eCollection Date: 2025-12-01 DOI:10.3390/jmahp13040058
Maria Lorenzi, Stephen Ebohon, Jennifer Kissner, Jedd Comiskey, Mayke Paap, Christine Bouchet, Andy Garnham, Erika Wissinger
{"title":"Network Meta-Analysis of Bevacizumab Gamma Versus Competing Interventions for Treating Neovascular Age-Related Macular Degeneration in the United Kingdom.","authors":"Maria Lorenzi, Stephen Ebohon, Jennifer Kissner, Jedd Comiskey, Mayke Paap, Christine Bouchet, Andy Garnham, Erika Wissinger","doi":"10.3390/jmahp13040058","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"13 4","pages":"58"},"PeriodicalIF":0.0000,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12641919/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of market access & health policy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/jmahp13040058","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
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.

Abstract Image

Abstract Image

Abstract Image

在英国,贝伐单抗γ与竞争干预治疗新生血管性年龄相关性黄斑变性的网络meta分析
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.90
自引率
0.00%
发文量
0
审稿时长
14 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书