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Five-Year Outcomes with Anti-Vascular Endothelial Growth Factor Treatment of Neovascular Age-Related Macular Degeneration: The Comparison of Age-Related Macular Degeneration Treatments Trials
Journal article   Open access   Peer reviewed

Five-Year Outcomes with Anti-Vascular Endothelial Growth Factor Treatment of Neovascular Age-Related Macular Degeneration: The Comparison of Age-Related Macular Degeneration Treatments Trials

Maureen G Maguire, Daniel F Martin, Gui-Shuang Ying, Glenn J Jaffe, Ebenezer Daniel, Juan E Grunwald, Cynthia A Toth, Frederick L Ferris III, Stuart L Fine and Comparison of Age-related Macular Degeneration Treatments Trials (CATT) Research Group
Ophthalmology (Rochester, Minn.), Vol.123(8), pp.1751-1761
08/2016
DOI: 10.1016/j.ophtha.2016.03.045
PMCID: PMC4958614
PMID: 27156698
url
https://doi.org/10.1016/j.ophtha.2016.03.045View
Published (Version of record) Open Access

Abstract

To describe outcomes 5 years after initiating treatment with bevacizumab or ranibizumab for neovascular age-related macular degeneration (AMD). Cohort study. Patients enrolled in the Comparison of AMD Treatments Trials. Patients were assigned randomly to ranibizumab or bevacizumab and to 1 of 3 dosing regimens. After 2 years, patients were released from the clinical trial protocol. At 5 years, patients were recalled for examination. Visual acuity (VA) and morphologic retinal features. Visual acuity was obtained for 647 of 914 (71%) living patients with average follow-up of 5.5 years. The mean number of examinations for AMD care after the clinical trial ended was 25.3, and the mean number of treatments was 15.4. Most patients (60%) were treated 1 time or more with a drug other than their assigned drug. At the 5-year visit, 50% of eyes had VA of 20/40 or better and 20% had VA of 20/200 or worse. Mean change in VA was -3 letters from baseline and -11 letters from 2 years. Among 467 eyes with fluorescein angiography, mean total lesion area was 12.9 mm(2), a mean of 4.8 mm(2) larger than at 2 years. Geographic atrophy was present in 213 of 515 (41%) gradable eyes and was subfoveal in 85 eyes (17%). Among 555 eyes with spectral-domain optical coherence tomography, 83% had fluid (61% intraretinal, 38% subretinal, and 36% sub-retinal pigment epithelium). Mean foveal total thickness was 278 μm, a decrease of 182 μm from baseline and 20 μm from 2 years. The retina was abnormally thin (<120 μm) in 36% of eyes. Between 2 and 5 years, the group originally assigned to ranibizumab for 2 years lost more VA than the bevacizumab group (-4 letters; P = 0.008). Otherwise, there were no statistically significant differences in VA or morphologic outcomes between drug or regimen groups. Vision gains during the first 2 years were not maintained at 5 years. However, 50% of eyes had VA of 20/40 or better, confirming anti-vascular endothelial growth factor therapy as a major long-term therapeutic advance for neovascular AMD.
Bevacizumab - therapeutic use Prospective Studies Follow-Up Studies Intravitreal Injections Geographic Atrophy - diagnosis Tomography, Optical Coherence Humans Male Treatment Outcome Wet Macular Degeneration - physiopathology Ranibizumab - therapeutic use Vascular Endothelial Growth Factor A - antagonists & inhibitors Wet Macular Degeneration - diagnosis Wet Macular Degeneration - drug therapy Subretinal Fluid Aged, 80 and over Angiogenesis Inhibitors - therapeutic use Female Aged Retina - pathology Visual Acuity - physiology Cohort Studies Fluorescein Angiography

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