Effectiveness and safety of ranibizumab in patients with central retinal vein occlusion: results from the real-world, global, LUMINOUS study.


Journal

Eye (London, England)
ISSN: 1476-5454
Titre abrégé: Eye (Lond)
Pays: England
ID NLM: 8703986

Informations de publication

Date de publication:
08 2022
Historique:
received: 14 12 2020
accepted: 15 07 2021
revised: 13 07 2021
pubmed: 31 7 2021
medline: 27 7 2022
entrez: 30 7 2021
Statut: ppublish

Résumé

To evaluate the effectiveness, treatment patterns and long-term safety of ranibizumab 0.5 mg in treatment-naïve patients with central retinal vein occlusion (CRVO) in a real-world setting. LUMINOUS, a 5-year, global, prospective, multicentre, multi-indication, observational, open-label study, recruited treatment naïve or prior treated patients who were treated as per the local ranibizumab label. Here, we report the mean change in visual acuity (VA; Early Treatment Diabetic Retinopathy Study [ETDRS] letters), treatment exposure over year (Y) 1 and 5-year safety in treatment-naïve CRVO patients. At baseline, the mean age of treatment-naïve CRVO patients (n = 327) was 68.9 years, with a mean (Standard deviation [SD]) VA of 40.6 (23.9) letters. At Y1, patients (n = 144) had a mean (SD) VA gain from baseline of 10.8 (19.66) letters, with a mean (SD) of 5.4 (2.65) ranibizumab injections. Patients demonstrated mean (SD) VA gains of 2.7 (19.35), 11.6 (20.56), 13.9 (18.08), 11.1 (18.46) and 8.2 (24.86) letters with 1, 2-3, 4-5, 6-8 and >8 ranibizumab injections, respectively. Mean (SD) VA gains at Y1 in patients receiving loading (67.4%) and no loading dose (32.6%) was 11.9 (20.42) and 8.4 (17.99) letters, respectively. Over five years, the incidence of ocular/non-ocular adverse events (AEs) and serious AEs was 11.3%/8.6% and 1.2%/6.7%, respectively. These results demonstrate the effectiveness of ranibizumab in treatment-naïve CRVO patients at Y1 with clinically meaningful VA gains and no new safety findings over five years. These findings may help inform routine practice and enable better clinical management to achieve optimal visual outcomes.

Identifiants

pubmed: 34326500
doi: 10.1038/s41433-021-01702-y
pii: 10.1038/s41433-021-01702-y
pmc: PMC9307792
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Ranibizumab ZL1R02VT79

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1656-1661

Informations de copyright

© 2021. The Author(s).

Références

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Auteurs

Andrew Lotery (A)

Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.

Andreas Clemens (A)

Novartis Pharma AG, Basel, Switzerland. andreas.clemens@novartis.com.
Department of Cardiology and Angiology I, Heart Center Freiburg University, Faculty of Medicine, University of Freiburg, Freiburg, Germany. andreas.clemens@novartis.com.

Raman Tuli (R)

Department of Ophthalmology, University of Ottawa, Ottawa, Canada.

Xun Xu (X)

Department of Ophthalmology, Shanghai First People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, China.

Masahiko Shimura (M)

Department of Ophthalmology, Tokyo Medical University Hachioji Medical Center, Hachioji-shi, Tokyo-To, Japan.

Marco Nardi (M)

Ophthalmology Unit, University of Pisa, Pisa, Italy.

Focke Ziemssen (F)

Department for Ophthalmology, Eberhard Karl University Tübingen, Tübingen, Germany.

Cornelia Dunger-Baldauf (C)

Novartis Pharma AG, Basel, Switzerland.

Ramin Tadayoni (R)

Université de Paris, Ophthalmology Department, AP-HP, Lariboisière, Saint Louis and Fondation Rothschild Hospitals, Paris, France.

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