Faricimab Treat-and-Extend Dosing for Macular Edema Due to Retinal Vein Occlusion. 72-Week Results from the BALATON and COMINO Trials

To assess the efficacy, durability, and safety of dual angiopoietin-2/VEGF inhibition with faricimab dosed per a modified treat-and-extend-based regimen in patients with retinal vein occlusion.Single-arm treatment period after a randomized, double-masked, active comparator-controlled period in the p...

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Bibliográfiai részletek
Szerzők: Danzig Carl J
Dinah Christiana
Ghanchi Faruque
Hattenbach Lars-Olof
Khanani Arshad M
Lai Timothy Y Y
Shimura Masahiko
Abreu Francis
Arrisi Pablo
Liu Ying
Paris Liliana P
Retiere Anne-Cecile
Willis Jeffrey R
Schlottmann Patricio G
Tóth-Molnár Edit
Dokumentumtípus: Cikk
Megjelent: 2025
Sorozat:OPHTHALMOLOGY RETINA 9 No. 9
Tárgyszavak:
doi:10.1016/j.oret.2025.03.005

mtmt:36852360
Online Access:http://publicatio.bibl.u-szeged.hu/38705
Leíró adatok
Tartalmi kivonat:To assess the efficacy, durability, and safety of dual angiopoietin-2/VEGF inhibition with faricimab dosed per a modified treat-and-extend-based regimen in patients with retinal vein occlusion.Single-arm treatment period after a randomized, double-masked, active comparator-controlled period in the phase III BALATON/COMINO (NCT04740905/NCT04740931) trials.Patients with treatment-naïve foveal center-involved macular edema due to branch (BALATON; N = 553) or central/hemiretinal (COMINO; N = 729) retinal vein occlusion.Patients randomized to faricimab 6.0 mg every 4 weeks (Q4W) or aflibercept 2.0 mg Q4W up to week 20 received faricimab 6.0 mg dosed per a modified treat-and-extend-based regimen from week 24 to 72. The dosing frequency was adjusted from Q4W to Q16W based on changes in central subfield thickness (CST) and best-corrected visual acuity.Change from baseline through week 72 in best-corrected visual acuity and CST; durability and safety through week 72.Visual acuity gains and CST reductions achieved at week 24 were maintained through week 72. Adjusted mean best-corrected visual acuity (95.03% confidence interval [CI]) changes from baseline averaged over weeks 64, 68, and 72 in the prior faricimab Q4W and prior aflibercept Q4W arms were +18.1 letters (16.9-19.4) and +18.8 letters (17.5-20.0), respectively, in BALATON and +16.9 letters (15.2-18.6) and +17.1 letters (15.4-18.8), respectively, in COMINO. Adjusted mean (95.03% CI) CST changes from baseline averaged over weeks 64, 68, and 72 in the prior faricimab Q4W and prior aflibercept Q4W arms were -310.9 μm (-315.6 to -306.3) and -307.0 μm (-311.7 to -302.3), respectively, in BALATON and -465.9 μm (-472.5 to -459.3) and -460.6 μm (-467.2 to -453.9), respectively, in COMINO. In the prior faricimab Q4W and prior aflibercept Q4W arms, 64.1% and 56.9% of patients from BALATON and 45.5% and 50.1% from COMINO, respectively, were on ≥Q12W dosing at week 68. Faricimab continued to be well tolerated from weeks 24 to 72; the safety profile was consistent with that established for diabetic macular edema and neovascular age-related macular degeneration.These findings support the sustained efficacy and safety of faricimab in patients with macular edema due to retinal vein occlusion up to 72 weeks, with the potential for reduced treatment burden due to response durability.Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
Terjedelem/Fizikai jellemzők:12
848-859
ISSN:2468-6530