Occlusive Retinal Vasculitis Following Intravitreal Brolucizumab.

To analyze a case series of retinal vasculitis reported to the American Society of Retina Specialists (ASRS) following Food and Drug Administration approval of brolucizumab for treatment of neovascular age-related macular degeneration. The ASRS Research and Safety in Therapeutics Committee analyzed clinical and imaging characteristics from submitted reports of retinal vasculitis after brolucizumab. Retinal vasculitis was reported in 26 eyes of 25 patients (22 [88%] female) after treatment with brolucizumab. Imaging studies were available for 24 of 26 eyes. Most cases (92%) were associated with intraocular inflammation, which presented at a mean of 25 days (range, 3-63 days) after the most recent brolucizumab injection. Mean visual acuity (VA) was 20/52 (range, 20/25-4/200) before the adverse event, 20/151 (range, 20/25-hand motion) at presentation of the adverse event, and 20/243 (range, 20/30-light perception) at last follow-up. Twelve eyes (46%) had a greater than 3-line decrease in VA at final follow-up, and 12 eyes (46%) had a final VA of 20/200 or worse. Analysis of retinal imaging identified vasculopathy that involved retinal arteries (91%), retinal veins (79%), and choroidal vessels (48%). Occlusive disease was apparent on imaging in 83% of eyes. Treatment approaches were varied. Retinal vasculitis has been identified in a series of eyes following brolucizumab. Although a few eyes in this series were asymptomatic or minimally symptomatic, some eyes had significant vision loss. A careful examination for signs of active inflammation prior to brolucizumab injection is recommended. Once vasculopathy is suspected, angiographic imaging may help define the spectrum of involvement. Optimal treatment strategies remain unknown.

Déclaration de conflit d'intérêts

Declaration of Conflicting Interests The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Relevant potential conflicts of interest are reported as follows: A.J.W.: none; P.H.: Genentech (consultant, lecture fees) and Allergan (consultant); T.G.M.: none; J.F.A.: Springer SBM LLC (patents/royalties), DORC International B.V. (consultant, lecture fees), Allergan Inc (consultant, lecture fees), Bayer (consultant, lecture fees), Mallinckrodt (consultant), and TOPCON (grant support); K.J.B.: Bausch&Lomb (consultant, lecture fees), Allergan (consultant, lecture fees), Regeneron (consultant, lecture fees), Novartis (consultant, lecture fees), and Genentech (consultant); N.C.: Allergan (consultant), Bayer (consultant), Novartis (consultant); G.G.E.: Novartis (stock), and Regeneron (stock); R.A.G: Genentech (research, speaker, advisory), Regeneron (advisory), Novartis (research, speaker, advisory), Allergan (research, speaker, advisory), Aerie (research), Santen (research), Graybug (research), and NovoNordisk (research); S.J.K.: none; J.P.: none; E.W.S.: none; H.T.: Alimera (stock); R.W.W.: Novartis (research).