Aflibercept for age-related macular degeneration: 4-year outcomes of a 'treat-and-extend' regimen with exit-strategy.
Angiogenesis Inhibitors
/ therapeutic use
Humans
Intravitreal Injections
Macular Degeneration
/ drug therapy
Receptors, Vascular Endothelial Growth Factor
/ therapeutic use
Recombinant Fusion Proteins
/ therapeutic use
Tomography, Optical Coherence
/ methods
Treatment Outcome
Visual Acuity
Wet Macular Degeneration
/ diagnosis
Neovascularisation
Retina
Vitreous
Journal
The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041
Informations de publication
Date de publication:
02 2022
02 2022
Historique:
received:
19
04
2020
revised:
20
08
2020
accepted:
11
10
2020
pubmed:
1
11
2020
medline:
23
4
2022
entrez:
31
10
2020
Statut:
ppublish
Résumé
To report long-term outcomes on best-corrected visual acuity (BCVA) and treatment intervals with a treat-and-extend (T&E) regimen in patients with neovascular age-related macular degeneration (nAMD). This observational study included treatment-naïve patients with nAMD, treated with aflibercept. A specific T&E protocol without a loading phase and predefined exit criteria was administered. After reaching predefined 'exit-criteria', the treatment period was complete, and patients were observed three monthly. Eighty-two patients with a follow-up period of ≥2 years were included. BCVA (mean±SD, ETDRS letters) increased from 51.9±25.2 at baseline to 63.7±17.7 (p<0.0001) at 1 year, 61.7±18.5 (p<0.0001) at 2 years, 62.4±19.5 (p<0.0001, n=61) at 3 years and remained insignificantly higher than baseline at 4 years at 58.5±24.3 (p=0.22). Central subfield thickness (mean±SD, μm) decreased significantly from 387.5±107.6 (p<0.0001) at baseline to 291.9±65.5 (p<0.0001) at 1 year, and remained significantly lower until 4 years at 289.0±59.4 (p<0.0001). Treatment intervals (mean±SD, weeks) could be extended up to 9.3±3.1 weeks at 1 year and remained at 11.2±3.5 weeks at 4 years. Twenty-nine (35%) patients reached exit criteria and continued with three monthly observation only. After 4 years of treatment, initial vision gains were maintained with a reasonable treatment burden, even without an initial loading phase. Our results on functional outcomes are comparable with large controlled studies.
Identifiants
pubmed: 33127830
pii: bjophthalmol-2020-316514
doi: 10.1136/bjophthalmol-2020-316514
pmc: PMC8788035
doi:
Substances chimiques
Angiogenesis Inhibitors
0
Recombinant Fusion Proteins
0
aflibercept
15C2VL427D
Receptors, Vascular Endothelial Growth Factor
EC 2.7.10.1
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
246-250Informations de copyright
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: AE: lecturer fees and travel support from Bayer, grant and educational support from Novartis, consultant for Allergan. MM: consultant – Bayer, Gensight, Zeiss; financial support – Bayer; employee – Isarna (CMO). SW: Allergan, Bayer, Novartis, Heidelberg Engineering, Hoya, Optos, Euretina. Martin Zinkernagel: Allergan, Bayer, Novartis, Heidelberg Engineering.
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