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Efficacy and Safety of bimekizumab in elderly patients: real-world multicenter retrospective study – IL PSO (Italian Landscape Psoriasis)

Authors :
D. Orsini
M. Megna
C. Assorgi
A. Balato
R. Balestri
N. Bernardini
A. Bettacchi
T. Bianchelli
L. Bianchi
G. Buggiani
M. Burlando
AMG. Brunasso
G. Caldarola
N. Cameli
A. Campanati
E. Campione
A. Carugno
K. Chersi
A. Conti
A. Costanzo
E. Cozzani
A. Cuccia
D. D’Amico
G. Dal Bello
E. G. Dall’Olio
P. Dapavo
C. De Simone
E. V. Di Brizzi
A. Di Cesare
V. Dini
M. Esposito
E. Errichetti
M. C. Fargnoli
C. S. Fiorella
A. Foti
Z. Fratton
F. M. Gaiani
P. Gisondi
R. Giuffrida
A. Giunta
C. Guarneri
A. Legori
F. Loconsole
P. Malagoli
A. Narcisi
M. Paolinelli
L. Potestio
F. Prignano
G. Rech
A. Rossi
N. Skroza
F. Trovato
M. Venturini
A. G. Richetta
G. Pellacani
A. Dattola
Source :
Journal of Dermatological Treatment, Vol 35, Iss 1 (2024)
Publication Year :
2024
Publisher :
Taylor & Francis Group, 2024.

Abstract

Purpose of the article: The aim of this multicenter observational study is to report data from real world on the use of bimekizumab in patients aged ≥ 65 years with moderate-to-severe plaque psoriasis. Elderly patients are poorly represented in clinical trials on bimekizumab for plaque psoriasis, and real-world studies are important to guide clinical choices.Materials and methods: A retrospective multicenter study was conducted in 33 dermatological outpatient clinics in Italy. Patients aged ≥ 65 years, with moderate-to-severe plaque psoriasis and treated with bimekizumab were enrolled. No exclusion criteria were applied. Bimekizumab was administered following the Italian Guidelines for the management of plaque psoriasis and according to the summary of product characteristics, in adult patients who were candidates for systemic treatments. Overall, 98 subjects were included, and received bimekizumab up to week 36. Clinical and demographic data were collected before the initiation of treatment with bimekizumab. At baseline and each dermatological examination (4, 16, and 36 weeks), clinical outcomes were measured by the following parameters: (1) PASI score; (2) site-specific (scalp, palmoplantar, genital, nail) Psoriasis Global Assessment (PGA). At each visit, the occurrence of any adverse events (AEs) was recorded, including serious AEs and AEs leading to bimekizumab discontinuation.Results: The mean PASI score was 16.6 ± 9.4 at baseline and significantly decreased to 4.3 ± 5.2 after 4 weeks (p

Details

Language :
English
ISSN :
09546634 and 14711753
Volume :
35
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Dermatological Treatment
Publication Type :
Academic Journal
Accession number :
edsdoj.7ef04e4cae9b4655894c0414dffd2eb3
Document Type :
article
Full Text :
https://doi.org/10.1080/09546634.2024.2393376