Journal
AMERICAN JOURNAL OF OPHTHALMOLOGY
Volume 148, Issue 1, Pages 43-58Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2009.01.024
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Funding
- GENENTECH INC, SOUTH SAN FRANCISCO, CALIFORNIA
- THE DEPARTMENT OF OPHTHALmology at the Bascom Palmer Eye Institute, Miami, Florida
- National Eye Institute, National Institutes of Health, Bethesda, Maryland [P30 EY014801]
- German Research Foundation (DFG), Bonn, Germany
- Novortis Ophthalmics
- Alcon Laboratories
- CoMentis
- Quark
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PURPOSE: To assess the long-term efficacy of a variable-dosing regimen with ranibizumab in the Prospective Optical Coherence Tomography (OCT) Imaging of Patients with Neovascular Age-Related Macular Degeneration (AMID) Treated with intraOcular Ranibizumab (PrONTO) Study, patients were followed for 2 years. DESIGN: A 2-year prospective, uncontrolled, variable-dosing regimen with intravitreal ranibizumab based on OCT. METHODS: In this open-label, prospective, single,center, uncontrolled clinical study, AMD patients with neovascularization involving the central fovea and a central retinal thickness (CRT) of at least 300 mu m as measured by OCT were enrolled to receive 3 consecutive monthly intravitreal injections of ranibizumab (0.5 mg) [Lucentis; Genentech Inc, South San Francisco, California, USA]. During the first year, retreatment with ranibizumab was performed at each monthly visit if any criterion was fulfilled such as an increase in OCT CRT of at least 100 mu m or a loss of 5 letters or more. During the second year, the retreatment criteria were amended to include retreatment if any qualitative increase in the amount of fluid was detected using OCT. RESULTS: Forty patients were enrolled and 37 completed the 2-year study. At month 24, the mean visual acuity (VA) improved by 11.1 letters (P < .001) and the OCT-CRT decreased by 212 mu m (P < .001). VA improved by 15 letters or more in 43% of patients. These VA and OCT outcomes were achieved with an average of 9.9 injections over 24 months. CONCLUSIONS: The PrONTO Study using an OCT guided variable-dosing regimen with intravitreal ranibizumab resulted in VA outcomes comparable with the outcomes from the phase III clinical studies, but fewer intravitreal injections were required. (Am J Ophthalmol 2009; 148:43-58. (C) 2009 by Elsevier Inc. All rights reserved.)
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