Can intravitreal aflibercept injection (IAI) be used as a prophylactic treatment against conversion to exudative age-related macular degeneration (eAMD) in high-risk eyes?
In a randomized, single-masked clinical trial of 128 patients at high risk for eAMD, there was no difference in the proportion of eyes converting to eAMD between the IAI (6 patients [9.5%]) and sham (7 patients [10.9%]) groups at month 24. Patients with eAMD for longer than 2 years in their fellow eye at baseline showed a lower conversion rate in the study eye compared with those with eAMD for no longer than 2 years in the fellow eye.
Although these findings do not support IAI as a prophylactic against conversion to eAMD, such prophylaxis is needed.
Anti–vascular endothelial growth factor (VEGF) agents may provide a prophylactic effect in high-risk eyes with intermediate dry age-related macular degeneration (AMD) against conversion to exudative AMD (eAMD), lowering the risk of vision loss.
To evaluate intravitreal aflibercept injection (IAI) as prophylaxis against the conversion to eAMD in high-risk eyes at 24 months.
Design, Setting, and Participants
This single-masked, sham-controlled, randomized clinical trial performed at 4 US clinical sites enrolled patients with intermediate AMD in 1 eye (study eye), defined as presence of more than 10 medium drusen (≥63 to <125 μm), at least 1 large druse (≥125 μm), and/or retinal pigmentary changes, and eAMD in the fellow eye. Patients were treated from June 23, 2015, to March 13, 2019.
Intravitreal aflibercept injection (2 mg) or sham quarterly injection for 24 months (1:1 randomization).
Main Outcomes and Measures
The primary end point was the proportion of patients with conversion to eAMD at month 24 characterized by development of choroidal neovascularization, as assessed by leakage on fluorescein angiography and fluid on spectral-domain optical coherence tomography by an independent masked reading center.
Of 128 patients enrolled, 127 (63 in the IAI group and 64 in the sham group) were included in the primary analysis (68 men [53.5%]; mean [SD] age, 76.5 [8.1] years). Baseline demographic and clinical characteristics were balanced between the groups. By month 24, 6 patients (9.5%) in the IAI group and 7 (10.9%) in the sham group developed eAMD (P = .98). Patients with a history of eAMD for longer than 2 years in their fellow eye at baseline showed a lower rate of conversion to eAMD in the study eye compared with those with a history of eAMD for 2 years or less in the fellow eye. Safety was consistent with previous studies involving intravitreal anti-VEGF injections.
Conclusions and Relevance
In this evaluation of quarterly anti-VEGF exposure as prophylaxis to reduce conversion of eyes with high-risk dry AMD to eAMD, the rates of conversion were not lower in the IAI group compared with the sham treatment group at month 24. Understanding the mechanism of conversion to eAMD and therapies that could prevent this event remains an important unmet need.
ClinicalTrials.gov Identifier: NCT02462889
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Heier JS, Brown DM, Shah SP, et al. Intravitreal Aflibercept Injection vs Sham as Prophylaxis Against Conversion to Exudative Age-Related Macular Degeneration in High-risk Eyes: A Randomized Clinical Trial. JAMA Ophthalmol. Published online March 18, 2021. doi:10.1001/jamaophthalmol.2021.0221
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