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Aflibercept for age-related macular degeneration: a game-changer or quiet addition?

Publication ,  Journal Article
Browning, DJ; Kaiser, PK; Rosenfeld, PJ; Stewart, MW
Published in: Am J Ophthalmol
August 2012

PURPOSE: To describe the pharmacokinetics, preclinical studies, and clinical trials of the newly approved anti-vascular endothelial growth factor (VEGF) drug aflibercept (Eylea (VEGF Trap-Eye); Regeneron; and Bayer). DESIGN: Review with editorial commentary. METHODS: A review of the medical literature and pertinent Internet postings combined with analysis of key studies with expert opinion regarding the use of aflibercept for the treatment of exudative age-related macular degeneration. RESULTS: Aflibercept, a fusion protein with binding domains from native VEGF receptors, binds VEGF-A, VEGF-B, and placental growth factors 1 and 2 with high affinity. Preclinical ophthalmologic studies demonstrated that aflibercept suppresses choroidal neovascularization in several animal models. The results of phase 1 and 2 trials showed excellent short-term suppression of choroidal neovascularization in patients with exudative age-related macular degeneration and suggested a longer durability of aflibercept compared with other anti-VEGF drugs. The pivotal phase 3 Vascular Endothelial Growth Factor (VEGF) Trap-Eye: Investigation of Efficacy and Safety in Wet Age-Related Macular Degeneration 1 and 2 trials showed that monthly and bimonthly aflibercept were noninferior to monthly ranibizumab at preventing vision loss (< 15-letter loss) with comparable vision gains and safety. Year 2 treatment involved monthly pro re nata injections with required injections every 3 months and maintained vision gains from the first year, with an average of 4.2 injections of aflibercept and 4.7 injections of ranibizumab. CONCLUSIONS: Aflibercept promises to deliver excellent visual outcomes for exudative age-related macular degeneration patients while undergoing fewer injections compared with ranibizumab. With a wholesale cost of $1850 per dose, the cost per patient with aflibercept treatment promises to be lower than with ranibizumab.

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Published In

Am J Ophthalmol

DOI

EISSN

1879-1891

Publication Date

August 2012

Volume

154

Issue

2

Start / End Page

222 / 226

Location

United States

Related Subject Headings

  • Vascular Endothelial Growth Factor A
  • Recombinant Fusion Proteins
  • Receptors, Vascular Endothelial Growth Factor
  • Ophthalmology & Optometry
  • Macular Degeneration
  • Humans
  • Drug Evaluation, Preclinical
  • Drug Approval
  • Clinical Trials as Topic
  • Animals
 

Citation

APA
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ICMJE
MLA
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Browning, D. J., Kaiser, P. K., Rosenfeld, P. J., & Stewart, M. W. (2012). Aflibercept for age-related macular degeneration: a game-changer or quiet addition? Am J Ophthalmol, 154(2), 222–226. https://doi.org/10.1016/j.ajo.2012.04.020
Browning, David J., Peter K. Kaiser, Philip J. Rosenfeld, and Michael W. Stewart. “Aflibercept for age-related macular degeneration: a game-changer or quiet addition?Am J Ophthalmol 154, no. 2 (August 2012): 222–26. https://doi.org/10.1016/j.ajo.2012.04.020.
Browning DJ, Kaiser PK, Rosenfeld PJ, Stewart MW. Aflibercept for age-related macular degeneration: a game-changer or quiet addition? Am J Ophthalmol. 2012 Aug;154(2):222–6.
Browning, David J., et al. “Aflibercept for age-related macular degeneration: a game-changer or quiet addition?Am J Ophthalmol, vol. 154, no. 2, Aug. 2012, pp. 222–26. Pubmed, doi:10.1016/j.ajo.2012.04.020.
Browning DJ, Kaiser PK, Rosenfeld PJ, Stewart MW. Aflibercept for age-related macular degeneration: a game-changer or quiet addition? Am J Ophthalmol. 2012 Aug;154(2):222–226.
Journal cover image

Published In

Am J Ophthalmol

DOI

EISSN

1879-1891

Publication Date

August 2012

Volume

154

Issue

2

Start / End Page

222 / 226

Location

United States

Related Subject Headings

  • Vascular Endothelial Growth Factor A
  • Recombinant Fusion Proteins
  • Receptors, Vascular Endothelial Growth Factor
  • Ophthalmology & Optometry
  • Macular Degeneration
  • Humans
  • Drug Evaluation, Preclinical
  • Drug Approval
  • Clinical Trials as Topic
  • Animals