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Ten-year outcomes of anti-vascular endothelial growth factor treatment for neovascular age-related macular disease: A single-centre French study.

Authors :
Wolff B
Macioce V
Vasseur V
Castelnovo L
Michel G
Nguyen V
Daien V
Mauget-Faÿsse M
Gillies M
Source :
Clinical & experimental ophthalmology [Clin Exp Ophthalmol] 2020 Jul; Vol. 48 (5), pp. 636-643. Date of Electronic Publication: 2020 Mar 16.
Publication Year :
2020

Abstract

Importance: Long-term data of intravitreal injections of vascular endothelial growth factor (VEGF) inhibitors are lacking.<br />Background: This study aims to assess visual and anatomic outcomes of eyes with neovascular age-related macular degeneration (nAMD) after 10 years of anti-VEGF therapy.<br />Design: Retrospective analysis of data from a prospectively designed database.<br />Participants: One hundred and sixteen eyes with nAMD (94 participants) that started anti-VEGF therapy at least 10 years earlier.<br />Methods: Eyes were tracked by the Fight Retinal Blindness! registry.<br />Main Outcome Measures: Mean change in visual acuity at 10 years vs baseline. Visual acuity was assessed by the number of letters read on a logarithm of the minimum angle of resolution chart.<br />Results: Eyes received a median of 27.5 injections over 10 years. Mean visual acuity was 57.5 letters (SD 17.5) at baseline. It increased slightly at 1 year, then dropped steadily by 18 letters (95% CI: 13.7; 22.3) at 10 years. Overall, 10% of eyes gained ≥10 letters, 64% lost ≥10 letters and 23% remained stable (±5 letters from baseline). Geographic atrophy and subretinal fibrosis were found in 93% and 71%, respectively, after 10 years, both mostly affecting the centre of the fovea. Pre-treated eyes (47.5%) had significantly worse visual acuity than treatment-naïve eyes at baseline and during follow-up and were significantly more likely to have atrophy and fibrosis.<br />Conclusions and Relevance: Despite short-term stabilization, long-term visual outcomes of nAMD eyes under anti-VEGF therapy may be poor. Development of atrophy and fibrosis, resulting from the natural progression of the disease, may partly explain this evolution.<br /> (© 2020 Royal Australian and New Zealand College of Ophthalmologists.)

Details

Language :
English
ISSN :
1442-9071
Volume :
48
Issue :
5
Database :
MEDLINE
Journal :
Clinical & experimental ophthalmology
Publication Type :
Academic Journal
Accession number :
32112667
Full Text :
https://doi.org/10.1111/ceo.13742