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Comparative Efficacy of Brolucizumab in the Treatment of Neovascular Age-Related Macular Degeneration: A Systematic Literature Review and Network Meta-Analysis.
Finger, Robert P; Dennis, Natalie; Freitas, Rita; Quenéchdu, Arthur; Clemens, Andreas; Karcher, Helene; Souied, Eric H.
Afiliación
  • Finger RP; Department of Ophthalmology, University of Bonn, Bonn, Germany. robert.finger@ukbonn.de.
  • Dennis N; Health Economics and Market Access, Amaris, Paris, France.
  • Freitas R; Novartis Farma-Produtos Farmacêuticos S.A., Porto Salvo, Portugal.
  • Quenéchdu A; Amaris, Health Economics and Market Access, Montréal, Canada.
  • Clemens A; Novartis Pharma AG, Basel, Switzerland.
  • Karcher H; Department of Cardiology and Angiology I, Faculty of Medicine, Heart Center Freiburg University, University of Freiburg, Freiburg, Germany.
  • Souied EH; Novartis Pharma AG, Basel, Switzerland.
Adv Ther ; 39(8): 3425-3448, 2022 08.
Article en En | MEDLINE | ID: mdl-35678996
ABSTRACT

INTRODUCTION:

A systematic literature review (SLR) and network meta-analysis (NMA) were conducted to evaluate the comparative efficacy of brolucizumab relative to other anti-vascular endothelial growth factor (VEGF) treatments for neovascular age-related macular degeneration (nAMD) at 1 and 2 years, and overall safety and injection frequency of each treatment.

METHODS:

An SLR identifying randomized controlled trials (RCTs) published before June 2021 according to a pre-specified protocol was followed by a Bayesian NMA to compare brolucizumab (6 mg q12w/q8w) against sham and all relevant anti-VEGF regimens. Pooled mean injection frequency, serious adverse ocular events, and discontinuation rates were estimated for each treatment regimen.

RESULTS:

Nineteen RCTs were included in NMA base-case analysis. Brolucizumab (6 mg q12w/q8w) with loading-phase (LP) demonstrated superior best-corrected visual acuity (BCVA) gains to sham both at year 1 (mean difference 16.8 [95%CrI 13.3, 20.4]) and year 2 (mean difference 21.2 [95%CrI 17.4, 25.0]) and was comparable to other anti-VEGFs. Brolucizumab (6 mg q12w/q8w) also showed superior retinal thickness reduction to most comparators including ranibizumab (0.5 mg q4w; year 1 mean difference - 50.1 [95%CrI - 70.3, - 29.8]; year 2 mean difference - 49.5 [95%CrI - 70.8, - 28.6]), aflibercept (2 mg q8w; year 1 mean difference - 39.7 [95%CrI - 52.9, - 26.4]; year 2 mean difference - 35.0 [95%CrI - 49.1, - 21.4]), and faricimab (6 mg q16w/q8w; year 1 mean difference - 27.6 [95%CrI - 42.3, - 12.8]). Brolucizumab (6 mg q12w/q8w) showed similar rates of treatment discontinuation and serious and overall adverse events (both years). At year 2, pooled annualized injection frequency was lowest for brolucizumab (6 mg q12w/q8w) and highest for ranibizumab (0.5 mg q4w) at 5.7 and 11.5 injections annually, respectively.

CONCLUSION:

Among all licensed anti-VEGF treatments, brolucizumab showed superior reduction in retinal thickness and comparable BCVA gains and discontinuation rates, despite having the lowest injection frequency. The current study provides the most up-to-date, robust comparison of treatments for nAMD.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ranibizumab / Degeneración Macular Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Systematic_reviews Límite: Child, preschool / Humans / Infant Idioma: En Revista: Adv Ther Asunto de la revista: TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ranibizumab / Degeneración Macular Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Systematic_reviews Límite: Child, preschool / Humans / Infant Idioma: En Revista: Adv Ther Asunto de la revista: TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: Alemania