Canakinumab as first-line biological therapy in Still's disease and differences between the systemic and the chronic-articular courses: Real-life experience from the international AIDA registry.
AOSD
adult onset Still’s disease
autoinflammatory diseases
biological therapy
interleukin-1
sJIA
systemic juvenile idiopathic arthritis
Journal
Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047
Informations de publication
Date de publication:
2022
2022
Historique:
received:
16
10
2022
accepted:
28
11
2022
entrez:
9
1
2023
pubmed:
10
1
2023
medline:
10
1
2023
Statut:
epublish
Résumé
Interleukin (IL)-1 inhibitors are largely employed in patients with Still's disease; in cases with refractory arthritis, IL-6 inhibitors have shown to be effective on articular inflammatory involvement. The aim of the present study is to assess any difference in the effectiveness of the IL-1β antagonist canakinumab prescribed as first-line biologic agent between the systemic and the chronic-articular Still's disease. Data were drawn from the retrospective phase of the AutoInflammatory Disease Alliance (AIDA) international registry dedicated to Still's disease. Patients with Still's disease classified according to internationally accepted criteria (Yamaguchi criteria and/or Fautrel criteria) and treated with canakinumab as first-line biologic agent were enrolled. A total of 26 patients (17 females, 9 males; 18 patients developing Still's disease after the age of 16 years) were enrolled; 16 (61.5%) patients suffered from the systemic pattern of the disease; 10 (38.5%) patients suffered from the chronic-articular type. No differences were observed between the systemic and the chronic-articular Still's disease in the frequency of complete response, of flares after the start of canakinumab ( Canakinumab used for Still's disease has been effective in controlling both clinical and laboratory manifestations disregarding the type of disease course when used as first-line biotechnological agent. These excellent results might have been further enhanced by the early start of IL-1 inhibition.
Identifiants
pubmed: 36619631
doi: 10.3389/fmed.2022.1071732
pmc: PMC9813488
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1071732Informations de copyright
Copyright © 2022 Vitale, Caggiano, Maggio, Lopalco, Emmi, Sota, La Torre, Ruscitti, Bartoloni, Conti, Fabiani, Mattioli, Gaggiano, Cardinale, Dagna, Campochiaro, Giacomelli, Balistreri, Laskari, Tufan, Ragab, Almaghlouth, Więsik-Szewczyk, Pereira, Frediani, Iannone, Sfikakis and Cantarini.
Déclaration de conflit d'intérêts
Payment or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing or educational events: LC, Novartis. PR, Sobi, Abbvie, Novartis Ely Lilly, and BMS. CC, Sobi Novartis, Jannsen, and Boehringer. EW-S, Novartis and Sobi. LD, Novartis, Sobi, Roche, Galapagos, Jannsen, and Pfizer. PS, Abbvie, UCB, Novartis, Lilly, Genesis, Enorasis, Amgen, and Yansen. Support for attending meetings and travel: CC, Novartis and Amgen. EW-S, Sobi. LD, Novartis. Participation on a Data Safety Monitoring Board or Advisory Board: CC, Boehringer. LD, Novartis. Consulting fees: LD, Novartis, SOBI, Roche, Galapagos, Jannsen, and Pfizer. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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