4.7 Article

Real-World Experience with Brolucizumab in Wet Age-Related Macular Degeneration: The REBA Study

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 10, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/jcm10132758

Keywords

age-related macular degeneration; anti-vascular endothelial growth factor; brolucizumab; exudation; switch therapy

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The study aimed to determine the efficacy and safety of intravitreal brolucizumab therapy for neovascular age-related macular degeneration in real-world settings. Results showed good anatomical and functional responses to the treatment, with two significant untoward events noted.
The aim of the present study was to determine the efficacy and safety of intravitreal brolucizumab therapy for neovascular age-related macular degeneration (AMD) in the real-world setting. The REBA study (real-world experience with brolucizumab in wet AMD) was a retrospective, observational, multicentric study that included 78 consecutive patients (105 eyes), with neovascular AMD, who received brolucizumab therapy. Both treatment-naive and switch-therapy patients were included. Switch therapy was based either on fluid recurrence, fluid recalcitrance, or inability to extend beyond q4/q6. All relevant data were collected. The primary outcome measure was change in best-corrected visual acuity (BCVA) over time. Secondary outcome measures included determination of change in central subfield thickness (CST) and complications. The mean baseline BCVA was 49.4 +/- 5.4 letters and 40 +/- 3.2 letters, and corresponding mean BCVA gain was +11.9 +/- 3.9 letters (p = 0.011) and +10.4 +/- 4.8 letters (p = 0.014) in the treatment-naive and switch-therapy groups, respectively. The change in CST was significantly decreased in the treatment-naive (p = 0.021) and the switch-therapy (p = 0.013) groups. The mean follow-up was 10.4 months in both groups. One patient in the switch-therapy group developed vascular occlusion and another a macular hole after the fifth brolucizumab injection. Both patients recovered uneventfully. In conclusion, patients showed a very good anatomical and functional response to brolucizumab therapy in the real world, regardless of prior treatment status, until the end of the follow-up period. Two significant untoward events were noted.

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