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Effectiveness and safety of bimekizumab for the treatment of plaque psoriasis: a real-life multicenter study—IL PSO (Italian landscape psoriasis)

Authors :
Luigi Gargiulo
Alessandra Narcisi
Luciano Ibba
Anna Balato
Luca Bianchi
Pina Brianti
Dario Buononato
Martina Burlando
Giacomo Caldarola
Anna Campanati
Elena Campione
Carlo G. Carrera
Andrea Carugno
Antonio Cristaudo
Francesco Cusano
Paolo Dapavo
Annunziata Dattola
Clara De Simone
Francesca M. Gaiani
Paolo Gisondi
Alessandro Giunta
Francesco Loconsole
Vincenzo Maione
Edoardo Mortato
Angelo V. Marzano
Martina Maurelli
Matteo Megna
Santo R. Mercuri
Annamaria Offidani
Diego Orsini
Aurora Parodi
Giovanni Pellacani
Luca Potestio
Pietro Quaglino
Antonio G. Richetta
Francesca Romano
Paolo Sena
Marina Venturini
Piergiorgio Malagoli
Antonio Costanzo
Source :
Frontiers in Medicine, Vol 10 (2023)
Publication Year :
2023
Publisher :
Frontiers Media S.A., 2023.

Abstract

IntroductionBimekizumab is a monoclonal antibody that targets Interleukin-17 A and F, approved for the treatment of moderate-to-severe plaque psoriasis. While bimekizumab has been evaluated in several phase-III clinical trials, real-world evidence is still very limited.MethodThis multicenter retrospective study included patients affected by plaque psoriasis treated with bimekizumab from May 1, 2022 to April 30, 2023, at 19 Italian referral hospitals. Patients affected by moderate-to-severe plaque psoriasis eligible for systemic treatments were included. The effectiveness of bimekizumab was evaluated in terms of reduction in psoriasis area and severity index (PASI) compared with baseline at weeks 4 and 16. The main outcomes were the percentages of patients achieving an improvement of at least 75% (PASI75), 90% (PASI90) and 100% (PASI100) in PASI score.ResultsThe study included 237 patients who received at least one injection of bimekizumab. One hundred and seventy-one patients and 114 reached four and 16 weeks of follow-up, respectively. Complete skin clearance was achieved by 43.3% and 75.4% of patients at weeks 4 and 16, respectively. At week 16, 86.8% of patients reported no impact on their quality of life. At week 16, there were no significant differences between bio-naïve and bio-experienced patients in terms of PASI75, PASI90 and PASI100. The most commonly reported adverse events (AEs) were oral candidiasis (10.1%). No severe AEs or AEs leading to discontinuation were observed throughout the study.ConclusionOur experience supports the effectiveness and tolerability of bimekizumab in a real-world setting with similar results compared with phase-III clinical trials.

Details

Language :
English
ISSN :
2296858X
Volume :
10
Database :
Directory of Open Access Journals
Journal :
Frontiers in Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.57a586330ad40f1847d355dbee4ceef
Document Type :
article
Full Text :
https://doi.org/10.3389/fmed.2023.1243843