# 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

PMC · DOI: 10.3390/jmahp13040058 · Journal of Market Access & Health Policy · 2025-11-19

## TL;DR

This study compares the effectiveness of bevacizumab gamma with other treatments for a type of eye disease in the UK.

## Contribution

The study introduces a network meta-analysis comparing bevacizumab gamma with other anti-VEGF therapies for neovascular age-related macular degeneration.

## Key findings

- Bevacizumab gamma showed similar efficacy to other anti-VEGF treatments in improving visual acuity.
- All treatments were similarly effective except for specific ranibizumab dosing regimens.
- Findings are based on 22 randomized controlled trials included in the analysis.

## 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.

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** Age-Related Macular Degeneration (MESH:D008268), Neovascular (MESH:D016510)
- **Chemicals:** faricimab (MESH:C000723200), Bevacizumab (MESH:D000068258), ranibizumab (MESH:D000069579)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Q12W

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12641919/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12641919/full.md

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Source: https://tomesphere.com/paper/PMC12641919