Real-World Experience Using Intravitreal Brolucizumab Alone or in Combination with Aflibercept in the Management of Neovascular Age-Related Macular Degeneration.

aflibercept age-related macular degeneration anti-VEGF brolucizumab intravitreal injection; optical coherence tomography

Journal

Clinical ophthalmology (Auckland, N.Z.)
ISSN: 1177-5467
Titre abrégé: Clin Ophthalmol
Pays: New Zealand
ID NLM: 101321512

Informations de publication

Date de publication:
2023
Historique:
received: 01 12 2022
accepted: 09 02 2023
entrez: 7 3 2023
pubmed: 8 3 2023
medline: 8 3 2023
Statut: epublish

Résumé

To evaluate real-world experience using intravitreal brolucizumab (IVBr), alone or in combination with aflibercept, in eyes with neovascular age-related macular degeneration (nAMD) treated previously with other inhibitors of VEGF (anti-VEGF). This was a retrospective study of all eyes with nAMD treated with IVBr on a treat-and-extend protocol at a single center. Best-corrected visual acuity (BCVA), optical coherence tomography (OCT) at baseline and final visit, and drug-related adverse events were analyzed. Eyes with recurrent macular fluid on IVBr every 8 weeks were treated with a combination therapy alternating between IVBr and aflibercept every month. Among 52 eyes (40 patients) on IVBr, all had been previously treated with other anti-VEGF therapy, with 73% having persistent macular fluid. After a mean follow-up of 46.2±27.4 weeks on IVBr, the mean treatment interval for intravitreal therapy increased to 8.8±2.1 weeks on IVBr from a baseline of 6.1±3.1 weeks ( In the real world, IVBr used to treat eyes with nAMD previously treated with other anti-VEGF therapies appears to be well tolerated and associated with an improvement in macular fluid, stabilization of BCVA, and/or increase in intravitreal treatment interval. Combination therapy alternating between IVBr and aflibercept monthly appears to be well tolerated and can be considered for eyes with macular fluid on IVBr every 8 weeks.

Identifiants

pubmed: 36880020
doi: 10.2147/OPTH.S399590
pii: 399590
pmc: PMC9984903
doi:

Types de publication

Journal Article

Langues

eng

Pagination

657-665

Informations de copyright

© 2023 Mehta et al.

Déclaration de conflit d'intérêts

Dr Glenn Yiu reports personal fees from AbbVie, Adverum, Alimera, Bausch & Lomb, Clearside, Endogena, Genentech, Gyroscope, Intergalactic, Iridex, Janssen, Myro, NGM Biopharmaceutical, Novartis, Regeneron, Thea, Topcon, and Zeiss, outside the submitted work. Professor Dr Susanna S Park reports grants from Roche/Novartis and Ophthea outside the submitted work. The authors report no other conflicts of interest directly related to this work.

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Auteurs

Neesurg Mehta (N)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.

Rodney D Fong (RD)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
University of Nevada, Reno School of Medicine, Reno, NV, USA.

Machelle Wilson (M)

Department of Public Health Sciences, Division of Biostatistics, University of California, Davis, CA, USA.

Kareem Moussa (K)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.

Parisa Emami-Naeini (P)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
Department of Ophthalmology, Veterans Administration Hospital, Mather, CA, USA.

Ala Moshiri (A)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.

Glenn Yiu (G)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.

Susanna S Park (SS)

Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.

Classifications MeSH