April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
One-Year Results of Ranibizumab for Exudative AMD in a Clinical Setting
Author Affiliations & Notes
  • M.-H. Nghiem-Buffet
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • L. Dubois
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • T. Ramin
    Ophthalmology, Hôpital Lariboisière, Paris, France
  • F. Fajnkuchen
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • C. Delahaye-Mazza
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • B. Guiberteau
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • G. Quentel
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • S. Y. Cohen
    Ophthalmology, Centre Ophtalmologique d'Imagerie et de Laser, Paris, France
  • Footnotes
    Commercial Relationships  M.-H. Nghiem-Buffet, None; L. Dubois, None; T. Ramin, None; F. Fajnkuchen, None; C. Delahaye-Mazza, None; B. Guiberteau, None; G. Quentel, None; S.Y. Cohen, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 2377. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      M.-H. Nghiem-Buffet, L. Dubois, T. Ramin, F. Fajnkuchen, C. Delahaye-Mazza, B. Guiberteau, G. Quentel, S. Y. Cohen; One-Year Results of Ranibizumab for Exudative AMD in a Clinical Setting. Invest. Ophthalmol. Vis. Sci. 2009;50(13):2377.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : To analyze the one-year results of ranibizumab in patients with subfoveal exudative AMD in a tertiary care center established in Western Europe, to compare these results with the pivotal studies (MARINA and ANCHOR), and to search factors of favorable outcome.

Methods: : Retrospective analysis of 122 consecutive patients (124 eyes) treated with intravitreal ranibizumab injections. None of these 124 eyes had undergone previous treatment. Change in visual acuity (VA) between baseline and week 52 +/- 6 was analyzed in regard to: age, gender, treated eye, subtype of choroidal neovascularization (classic vs occult), initial protocol (one or 3 initial injections, followed by re-injections decided as needed, based on OCT and VA findings).

Results: : At 52 weeks, mean VA remained stable (+0.7 letters), changing from 56.15 (+/-14) to 56.89 (+/-17) letters on ETDRS chart comparing with a mean improvement of +7.2 letters (MARINA) and 11.3 letters (ANCHOR). 90.3 % of the eyes lost fewer than 15 letters as compared with 94.6% (MARINA) and 96.4% (ANCHOR). Visual acuity improved by 15 or more letters in 8% of the eyes as compared with 33.8% (MARINA) and 40.3% (ANCHOR). At last follow-up, VA was 20/40 or more in 25.8% of the eyes as compared with 40% (MARINA) and 40.3% (ANCHOR). Age, gender, treated eye, type of CNV and protocol of initial management did not have an influence on final results.The mean number of injections per eye was 3.79 and the mean number of visits was 8.06 as compared with the 12 visits and injections in pivotal studies.

Conclusions: : In the present study, mean number of injections was significantly smaller than in pivotal studies. But the results compare unfavorably with these studies. This difference could be explained by inclusion of patients with a VA out of the 20/320-20/50 range and, mostly, by a follow-up which appeared to be far less tight than in pivotal studies.The present study suggests that a closer follow-up of patients treated by ranibizumab is necessary to obtain and keep significant visual improvement, as shown in pivotal studies.

Keywords: age-related macular degeneration • vascular endothelial growth factor • retinal neovascularization 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×