Switching to brolucizumab from aflibercept in age-related macular degeneration with type 1 macular neovascularization and polypoidal choroidal vasculopathy: an 18-month follow-up study

Purpose To assess the effect of switching to brolucizumab from aflibercept on eyes with type 1 macular neovascularization (MNV) and polypoidal choroidal vasculopathy (PCV) at 18 months. Methods This study was a retrospective, observational case series that included 19 eyes of 19 patients with type 1MNV and 23 eyes of 22 patients with PCV. We compared the injection intervals, visual acuity, total lesion size, and the number of polypoidal lesions between baseline and 18 months. The correlations between the data including treatment interval, total lesion size, and the number of polyps were also assessed. Results Treatment intervals were significantly extended; from 7.4 +/- 1.4 weeks to 11.6 +/- 2.6 weeks for type 1 MNV, p < 0.001; from 6.9 +/- 1.3 to 11.7 +/- 3.1 weeks for PCV, p < 0.001. In type 1 MNV eyes, strong correlation was found between total lesion size and brolucizumab injection intervals (r= - 0 .81 ; p = 0.0002) and moderate correlation was found between treatment frequency with aflibercept and that with brolucizumab (r = 0.76; p= 0.040). In PCV eyes, we found strong correlation between the number of polyps and brolucizumab treatment frequency (r= - 0.81; p = 0.0016) and moderate correlation between total lesion size and brolucizumab treatment interval (r= - 0.48; p= 0.034). Intraocular inflammation occurred in 2 of 19 eyes (10.3%) with type 1 MNV and 5 of 23 eyes (21.7%) with PCV. Conclusion The properties to extend brolucizumab injection intervals might be the smaller lesion size and lower aflibercept frequency for type 1 MNV and the smaller number of polyps and the smaller size of lesion for PCV.

Automated summary

This study assessed the effects of switching to brolucizumab from aflibercept on eyes with type 1 macular neovascularization (MNV) and polypoidal choroidal vasculopathy (PCV). The results show that brolucizumab can extend the injection intervals and is correlated with lesion size, treatment frequency, and the number of polyps.