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Incidence of choroidal neovascularization in the fellow eye in the comparison of age-related macular degeneration treatments trials
Journal article   Open access   Peer reviewed

Incidence of choroidal neovascularization in the fellow eye in the comparison of age-related macular degeneration treatments trials

Maureen G Maguire, Ebenezer Daniel, Ankoor R Shah, Juan E Grunwald, Stephanie A Hagstrom, Robert L Avery, Jiayan Huang, Revell W Martin, Daniel B Roth, Alessandro A Castellarin, …
Ophthalmology (Rochester, Minn.), Vol.120(10), pp.2035-2041
10/2013
DOI: 10.1016/j.ophtha.2013.03.017
PMCID: PMC3758381
PMID: 23706946
url
http://doi.org/10.1016/j.ophtha.2013.03.017View
Open Access

Abstract

To assess the influence of drug; dosing regimen; and traditional, nontraditional, and genetic risk factors on the incidence of choroidal neovascularization (CNV) in the fellow eye of patients treated for CNV with ranibizumab or bevacizumab. Cohort study of patients enrolled in a multicenter, randomized clinical trial. Patients with no CNV in the fellow eye at the time of enrollment in the Comparison of Age-Related Macular Degeneration Treatments Trials (CATT). Eligibility criteria for the clinical trial required that study eyes have evidence on fluorescein angiography and optical coherence tomography of CNV secondary to age-related macular degeneration (AMD) and visual acuity between 20/25 and 20/320. Treatment for the study eye was assigned randomly to either ranibizumab or bevacizumab and to 3 different regimens for dosing over a 2-year period. The genotypes for 4 single nucleotide polymorphisms (SNPs) associated with risk of AMD were determined. Only patients without CNV in the fellow eye at baseline were considered at risk. The CATT ophthalmologists examined patients every 4 weeks through 2 years and recorded treatment for CNV in the fellow eye. Development of CNV in the fellow eye. Among 1185 CATT participants, 727 (61%) had no CNV in the fellow eye at enrollment. At 2 years, CNV had developed in 75 (20.6%) of 365 patients treated with ranibizumab and in 60 (16.6%) of 362 patients treated with bevacizumab (absolute difference, 4.0%; 95% confidence interval [CI], -1.7% to 9.6%; P = 0.17). The risk ratio for pro re nata dosing relative to monthly dosing was 1.1 (95% CI, 0.8-1.6). Greater elevation of the retinal pigment epithelium and fluid in the foveal center of the study eye were associated with increased incidence of CNV in the fellow eye. Incidence was not associated with genotype on rs1061170 (CFH), rs10490924 (ARMS2), rs11200638 (HTRA1), and rs2230199 (C3; P>0.35). Through 2 years, there was no statistically significant difference between ranibizumab and bevacizumab in incidence of CNV in the fellow eye. Genotype on 4 SNPs previously found to be associated with AMD did not affect the risk of CNV in the fellow eye among CATT patients. Proprietary or commercial disclosure may be found after the references.
Choroidal Neovascularization - epidemiology Intravitreal Injections Humans Middle Aged Male Macular Degeneration - drug therapy Bevacizumab Incidence Dose-Response Relationship, Drug Choroidal Neovascularization - drug therapy Choroidal Neovascularization - pathology Ranibizumab Serine Endopeptidases - genetics Aged, 80 and over Angiogenesis Inhibitors - therapeutic use Female Complement C3 - genetics Genetic Predisposition to Disease Antibodies, Monoclonal, Humanized - therapeutic use Macular Degeneration - complications High-Temperature Requirement A Serine Peptidase 1 Genotype Proteins - genetics Macular Degeneration - genetics Aged Polymorphism, Single Nucleotide Complement Factor H - genetics Choroidal Neovascularization - genetics Cohort Studies

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