Ranibizumab 0.5 mg treat-and-extend regimen for diabetic macular oedema: the RETAIN study
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
26453639
PubMed Central
PMC4893084
DOI
10.1136/bjophthalmol-2015-307249
PII: bjophthalmol-2015-307249
Knihovny.cz E-zdroje
- Klíčová slova
- Clinical Trial, Macula, Treatment Lasers, Treatment Medical, Vision,
- MeSH
- časové faktory MeSH
- diabetická retinopatie komplikace diagnóza MeSH
- inhibitory angiogeneze aplikace a dávkování MeSH
- injekce intravitreální MeSH
- jednoduchá slepá metoda MeSH
- lidé středního věku MeSH
- lidé MeSH
- macula lutea diagnostické zobrazování MeSH
- makulární edém diagnóza farmakoterapie etiologie MeSH
- následné studie MeSH
- optická koherentní tomografie MeSH
- ranibizumab aplikace a dávkování MeSH
- retrospektivní studie MeSH
- vaskulární endoteliální růstový faktor A antagonisté a inhibitory MeSH
- výsledek terapie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zraková ostrost * MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- inhibitory angiogeneze MeSH
- ranibizumab MeSH
- vaskulární endoteliální růstový faktor A MeSH
AIMS: To demonstrate non-inferiority of ranibizumab treat-and-extend (T&E) with/without laser to ranibizumab pro re nata (PRN) for best-corrected visual acuity (BCVA) in patients with diabetic macular oedema (DMO). METHODS: A 24-month single-masked study with patients randomised 1:1:1 to T&E+laser (n=121), T&E (n=128) or PRN (control; n=123). All patients received monthly injections until BCVA stabilisation. The investigator decided on re-treatment in the PRN and treatment-interval adaptations in the T&E groups based on loss of BCVA stability due to DMO activity. Likewise, laser treatment was at investigator's discretion. Collectively, these features reflect a real-life scenario. Endpoints included mean average change in BCVA from baseline to months 1-12 (primary), mean BCVA change from baseline to months 12 and 24, treatment exposure and safety profile. RESULTS: Both T&E regimens were non-inferior to PRN based on mean average BCVA change from baseline to months 1-12 (T&E+laser: +5.9 and T&E: +6.1 vs PRN: +6.2 letters; both p<0.0001). Mean BCVA change at month 24 was similar across groups (+8.3, +6.5 and +8.1 letters, respectively). The mean number of injections was 12.4 and 12.8 in the T&E+laser and T&E groups and 10.7 in the PRN group. The T&E regimens showed 46% reduction in the number of clinic visits. Over 70% of patients maintained their BCVA, with treatment intervals of ≥2 months over 24 months. Safety profile was consistent with that described in the product information. CONCLUSIONS: T&E is a feasible treatment option for patients with DMO, with a potential to reduce treatment burden. Slightly more injections were required versus PRN, likely due to the specifics of the T&E regimen applied here. TRIAL REGISTRATION NUMBER: NCT01171976.
Centre d'Imagerie et Laser Paris France
Department of Ophthalmology University Hospital Hradec Králové Czech Republic
Department of Ophthalmology Vista Klinik Binningen Switzerland University of Basel Basel Switzerland
Novartis Pharma AG Basel Switzerland
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ClinicalTrials.gov
NCT01171976