Injection burden and treatment intervals of aflibercept in observe-and-plan regimen for neovascular age-related macular degeneration.

aflibercept neovascular age‐related macular degeneration observe‐and‐plan real‐world data treatment regimen

Journal

Acta ophthalmologica
ISSN: 1755-3768
Titre abrégé: Acta Ophthalmol
Pays: England
ID NLM: 101468102

Informations de publication

Date de publication:
11 May 2024
Historique:
received: 29 01 2024
accepted: 30 04 2024
medline: 11 5 2024
pubmed: 11 5 2024
entrez: 11 5 2024
Statut: aheadofprint

Résumé

The Observe-and-Plan (O&P) regimen allows for individualised treatment. In this study, we evaluated injection burden and intervals using aflibercept in an O&P regimen for eyes with neovascular age-related macular degeneration (AMD). This was a retrospective registry-based study of treatment-naïve eyes with neovascular AMD. Treatment data were compiled for 3 years after commencement of intravitreal aflibercept therapy. We evaluated clinical consequences at the first follow-up after loading dose, the proportion of patients who obtained and kept dry macula after loading dose, number of injections and intervals between injections. Data were obtained for 1103 eyes. After loading dose, 0.4% were lost to follow-up, 7.5% discontinued, 50.9% booked for further injections and 41.3% booked for monthly observations. After loading dose, the macula remained dry in 49.2% at 3 months, 34.0% at 6 months, 23.7% at 12 months and 15.2% at 24 months. For the entire population, median cumulative total number of injections was 7, 12 and 15, after 1, 2 and 3 years, respectively. After the 3rd year, the proportion of eyes in the short 4-6 weeks treatment interval was 51.1%, 8 weeks interval was kept in 14.4% and the extended treatment intervals of 10 and 12 weeks was possible in 34.4%. After loading dose, one in two eyes required further injections. A large proportion required therapy with shorter intervals than the label-recommended 8 weeks. The large majority of those who obtained a dry macula after loading dose turned exudative again, mostly within the first 3 months.

Identifiants

pubmed: 38733136
doi: 10.1111/aos.16709
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Acta Ophthalmologica Scandinavica Foundation. Published by John Wiley & Sons Ltd.

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Auteurs

Yousif Subhi (Y)

Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
Department of Ophthalmology, Zealand University Hospital, Roskilde, Denmark.
Department of Clinical Research, University of Southern Denmark, Odense, Denmark.

Miklos Schneider (M)

Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
Department of Ophthalmology, Semmelweis University, Budapest, Hungary.

Javad Nouri Hajari (JN)

Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Morten la Cour (M)

Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Classifications MeSH