Real-world Safety and Efficacy of Risankizumab in Psoriatic Patients: A Multicenter, Retrospective, and Not-interventional Study.

[[Artículo traducido]]Eficacia y seguridad del risankizumab en pacientes con psoriasis en el mundo real: un estudio retrospectivo, multicéntrico y no intervencionista.
Datos del mundo real Monoclonal antibody Psoriasis Psoriasis Area and Severity Index (PASI) Real-world data Risankizumab anticuerpo monoclonal Índice de Área y Severidad de la Psoriasis (PASI)

Journal

Actas dermo-sifiliograficas
ISSN: 1578-2190
Titre abrégé: Actas Dermosifiliogr
Pays: Spain
ID NLM: 0373062

Informations de publication

Date de publication:
23 Oct 2024
Historique:
received: 25 01 2024
accepted: 24 02 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

risankizumab-a humanized monoclonal antibody that targets the p19 subunit of IL-23-has been recently approved to treat moderate-to-severe plaque psoriasis. Real-world data based on a representative pool of patients are currently lacking. Objective To assess the mid- and long-term safety and efficacy profile of risankizumab in patients with moderate-to-severe psoriasis in the routine clinical practice. This was a retrospective and multicenter study of consecutive psoriatic patients on risankizumab from April 2020 through November 2022. The primary endpoint was the number of patients who achieved a 100% improvement in their Psoriasis Area and Severity Index (PASI) (PASI100) on week 52. A total of 510 patients, 198 (38.8%) women and 312 (61.2%) men were included in the study. The mean age was 51.7 ± 14.4 years. A total of 227 (44.5%) study participants were obese (body mass index [BMI] > 30kg/m Risankizumab proved to be a safe and effective therapy for patients with moderate-to-severe psoriasis in the routine clinical practice.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
risankizumab-a humanized monoclonal antibody that targets the p19 subunit of IL-23-has been recently approved to treat moderate-to-severe plaque psoriasis. Real-world data based on a representative pool of patients are currently lacking. Objective To assess the mid- and long-term safety and efficacy profile of risankizumab in patients with moderate-to-severe psoriasis in the routine clinical practice.
METHODS METHODS
This was a retrospective and multicenter study of consecutive psoriatic patients on risankizumab from April 2020 through November 2022. The primary endpoint was the number of patients who achieved a 100% improvement in their Psoriasis Area and Severity Index (PASI) (PASI100) on week 52.
RESULTS RESULTS
A total of 510 patients, 198 (38.8%) women and 312 (61.2%) men were included in the study. The mean age was 51.7 ± 14.4 years. A total of 227 (44.5%) study participants were obese (body mass index [BMI] > 30kg/m
CONCLUSIONS CONCLUSIONS
Risankizumab proved to be a safe and effective therapy for patients with moderate-to-severe psoriasis in the routine clinical practice.

Identifiants

pubmed: 39454868
pii: S0001-7310(24)00854-8
doi: 10.1016/j.ad.2024.10.042
pii:
doi:

Types de publication

Journal Article

Langues

eng spa

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 AEDV. Publicado por Elsevier España, S.L.U. All rights reserved.

Auteurs

A Martorell (A)

Department of Dermatology, Hospital de Manises, Valencia, Spain. Electronic address: martorelldermatologia@gmail.com.

S Santos-Alarcón (S)

Department of Dermatology, Hospital Virgen de los Lirios, Alcoy, Spain.

A Sahuquillo-Torralba (A)

Department of Dermatology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.

R Rivera-Díaz (R)

Department of Dermatology, Hospital Universitario 12 de Octubre, Madrid, Spain.

I Belinchón-Romero (I)

Department of Dermatology, Hospital General Universitario de Alicante, Spain.

D Ruiz-Genao (D)

Department of Dermatology, Hospital Universitario de Alcorcón, Madrid, Spain.

A Romero-Maté (A)

Department of Dermatology, Hospital Universitario de Fuenlabrada, Madrid, Spain.

R Ruiz-Villaverde (R)

Department of Dermatology, Hospital Universitario PTS, Granada, Spain.

M Ferrán-Farrés (M)

Department of Dermatology, Hospital del Mar, Barcelona, Spain.

F Gallardo-Hernández (F)

Department of Dermatology, Hospital del Mar, Barcelona, Spain.

M Almenara-Blasco (M)

Department of Dermatology, Hospital Universitario Miguel Servet, Zaragoza, Spain.

J Alonso-Suárez (J)

Department of Dermatology, Hospital Clínico Universitario Virgen de la Victoria, Málaga, Spain.

Á González-Cantero (Á)

Department of Dermatology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

E Martínez-Lorenzo (E)

Department of Dermatology, Hospital Universitario de Toledo, Spain.

J M Fernández-Armenteros (JM)

Department of Dermatology, Hospital Arnau de Vilanova de Lleida, Barcelona, Spain.

E de Alcázar-Viladomiu (E)

Department of Dermatology, Hospital Universitario Trias i Pujol, Barcelona, Spain.

J García-Latasa (J)

Department of Dermatology, Hospital Royo Villanova, Zaragoza, Spain.

V Rocamora-Durant (V)

Department of Dermatology, Hospital de Manacor, Mallorca, Spain.

M Ara-Martín (M)

Department of Dermatology, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.

A Mateu-Puchades (A)

Department of Dermatology, Hospital Universitario Doctor Peset, Valencia, Spain.

M Llamas-Velasco (M)

Department of Dermatology, Hospital de la Princesa, Madrid, Spain.

E Vilarrasa-Rull (E)

Department of Dermatology, Hospital Sant Pau, Barcelona, Spain.

M Velasco-Pastor (M)

Department of Dermatology, Arnau de Vilanova, Valencia, Spain.

P De la Cueva (P)

Department of Dermatology, Hospital Universitario Infanta Leonor, Madrid, Spain.

J M Carrascosa (JM)

Department of Dermatology Hospital Universitari Germans Trias i Pujol (HUGiT), Spain.

J Magdaleno-Tapial (J)

Department of Dermatology, Hospital General Universitario de Valencia, Valencia, Spain.

Classifications MeSH