May 2007
Volume 48, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2007
Efficacy of Intravitreal Bevacizumab (AvastinTM) vs. Ranibizumab (LucentisTM) as First Line Monotherapy for the Treatment of Neovascular Age-Related Macular Degeneration
Author Affiliations & Notes
  • N. J. Sund
    Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan
  • M. M. Lai
    Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan
  • A. Capone, Jr.
    Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan
  • T. S. Hassan
    Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan
  • Footnotes
    Commercial Relationships N.J. Sund, None; M.M. Lai, None; A. Capone, Genentech, Inc, R; Genentech, Inc, C; T.S. Hassan, Genentech, Inc, C; Genentech, Inc, R.
  • Footnotes
    Support None.
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 1813. doi:
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    • Get Citation

      N. J. Sund, M. M. Lai, A. Capone, Jr., T. S. Hassan; Efficacy of Intravitreal Bevacizumab (AvastinTM) vs. Ranibizumab (LucentisTM) as First Line Monotherapy for the Treatment of Neovascular Age-Related Macular Degeneration. Invest. Ophthalmol. Vis. Sci. 2007;48(13):1813.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose:: To report the safety and efficacy of intravitreal Avastin (Genentech, Inc) and Lucentis (Genentech, Inc) as first line monotherapy in the treatment of neovascular AMD.

Methods:: Retrospective, comparative analyses of patients with neovascular AMD treated with either intravitreal 0.5 mg Lucentis, or 1.25mg Avastin. Inclusion criteria consisted of patients >50 years of age with choroidal neovascularization secondary to AMD of all angiographic subtypes, locations, sizes, and Snellen visual acuities (VA) of 20/20 to 20/800. Patients with prior verteporforin photodynamic therapy, laser, or intravitreal or periocular injections were excluded. The primary efficacy endpoint was the proportion of patients who lost less than 3 lines from baseline VA at the last follow-up visit. Secondary VA endpoints included the proportion of patients who had gained 2 or more lines, and the mean change from baseline VA. LogMar converted VAs were used for statistical comparisons.

Results:: Ninety-seven eyes of 89 patients were included in the study. Avastin was given to 44 eyes and Lucentis to 53 eyes. Pre-injection characteristics were similar for both groups. Mean VA - Avastin group = 20/113 (range, 20/25-20/800), Lucentis group = 20/117 (range, 20/20-20/800); Lesion characteristics - Avastin group = 74% occult and 26% classic, Lucentis group = 78% occult and 22% classic; Mean lesion size determined by fluorescein angiography - Avastin group = 2.6 disc areas (DA, range, 0.5-16), Lucentis group = 2.4 DA (range, 1-12). A mean of 1.8 injections (range, 1-3) were given in the Avastin group and 2.0 injections (range, 1-3) in the Lucentis group. Mean follow-up was 113 days (range, 7-315) in the Avastin group, compared to 44 days (range, 6-122) in the Lucentis group. At the last follow-up visit, 97.7% of those given Avastin and 96.2% of those given Lucentis lost fewer than 3 Snellen lines. VA improved by more than 2 lines in 31.8% of the Avastin group compared to 39.6% in the Lucentis group. Mean VA increased by 0.8 lines in the Avastin group and by 0.7 lines in the Lucentis group (P=0.87, student’s t-test). No serious ocular or systemic complications were noted in either group.

Conclusions:: In this single-center non-randomized series, Avastin and Lucentis showed comparable efficacy as first line monotherapy for the treatment of neovascular AMD in terms of VA outcomes in the short term. A large, prospective, randomized clinical trial, with longer follow-up, is necessary to better compare these drugs for the treatment of all subtypes of neovascular AMD.

Keywords: age-related macular degeneration • clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials 
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