Switch to Aflibercept in the Treatment of Neovascular AMD: One-Year Results in Clinical Practice

• Tipo: Artigo em Revista Científica Internacional
• Data: 2015

Autores

Pinheiro Costa, J (Autor) Outra; Costa, JM (Autor) Outra; Beato, JN (Autor) Outra; Freitas da Costa, P (Autor) Outra; Brandao, E (Autor) Outra; Manuel Falcão (Autor) FMUP; Falcão-Reis F (Autor) FMUP; Ângela Carneiro (Autor) FMUP

Revista

Título: Ophthalmologica

Vol. 233

Páginas: 155-161

ISSN: 0030-3755

Editora: Karger

Indexação

ISI Web of Knowledge - 39 Citações

Scopus - 39 Citações

Outras Informações

ID Authenticus: P-00G-BHZ

DOI: 10.1159/000381221

Abstract (EN): Purpose: To report the clinical outcomes of intravitreal aflibercept therapy in eyes with refractory and recurrent neovascular age-related macular degeneration (AMD) switched from intravitreal bevacizumab or ranibizunnab. Methods: This is a retrospective review of eyes with neovascular AMD switched to intravitreal aflibercept with at least 1 year of follow-up after the switch. All patients had had a minimum of 3 injections of bevacizumab or ranibizumab before the switch. Aflibercept was used in patients considered refractory to bevacizumab (group 1) and in recurrent patients on therapy with ranibizumab due to an institutional policy decision (group 2). Changes in best-corrected visual acuity, fluid on optical coherence tomography (OCT), central retinal thickness (CRT) and the frequency of injections were compared. Results: Eighty-five eyes of 69 patients were analyzed, 39 eyes in group 1 and 46 in group 2. The mean follow-up time was 31.6 months prior to the switch and 14.7 months on treatment with aflibercept. One year after the switch, there was a nonsignificant mean decrease of 2 letters in visual acuity in both groups (group 1: from 58.2 to 55.8 letters, p = 0.086; group 2: from 56.4 to 54.5 letters, p = 0.168), but the mean number of injections per month was significantly lower (from 0.76 to 0.57, p<0.001). With the switch, 90.6% of the patients showed anatomic improvement with a reduction of fluid on OCT, and both groups presented significant improvement in CRT (group 1: 65.3 mu m, p = 0.051; group 2: 91.0 mu m, p < 0.001). Conclusion: Aflibercept appears to be a valuable tool for the management of patients with poor responses to other anti-vascular endothelial growth factor drugs. These patients could have anatomic improvement, and the injection intervals could be extended. (C) 2015 S. Karger AG, Basel

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 7