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Real-World Experience Using Intravitreal Brolucizumab Alone or in Combination with Aflibercept in the Management of Neovascular Age-Related Macular Degeneration.
Mehta, Neesurg; Fong, Rodney D; Wilson, Machelle; Moussa, Kareem; Emami-Naeini, Parisa; Moshiri, Ala; Yiu, Glenn; Park, Susanna S.
Afiliação
  • Mehta N; Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
  • Fong RD; Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
  • Wilson M; University of Nevada, Reno School of Medicine, Reno, NV, USA.
  • Moussa K; Department of Public Health Sciences, Division of Biostatistics, University of California, Davis, CA, USA.
  • Emami-Naeini P; Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
  • Moshiri A; Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
  • Yiu G; Department of Ophthalmology, Veterans Administration Hospital, Mather, CA, USA.
  • Park SS; Department of Ophthalmology and Vision Science, University of California Davis Health, Sacramento, CA, USA.
Clin Ophthalmol ; 17: 657-665, 2023.
Article em En | MEDLINE | ID: mdl-36880020
ABSTRACT

Purpose:

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).

Methods:

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.

Results:

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 (p<0.001). Macular fluid decreased and BCVA was stable/improved in 61.5% of eyes on IVBr. Ten eyes with increased macular fluid on IVBr monotherapy when extended to every 8 weeks were treated with combination therapy alternating between IVBr and aflibercept every 4 weeks. In these eyes, 80% had improved macular fluid on OCT and 70% stable or improved BCVA after a median follow-up of 53 weeks on combination therapy. Mild intraocular inflammation developed in four eyes, all occurring on IVBr monotherapy, and none had associated vision loss.

Conclusion:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: Clin Ophthalmol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: Clin Ophthalmol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos