Comparison of drug retention of TNF inhibitors, other biologics and JAK inhibitors in RA patients who discontinued JAK inhibitor therapy.
Humans
Janus Kinase Inhibitors
/ therapeutic use
Tumor Necrosis Factor Inhibitors
/ therapeutic use
Biological Products
/ therapeutic use
Arthritis, Rheumatoid
/ drug therapy
Prospective Studies
Treatment Outcome
Tumor Necrosis Factor-alpha
Antirheumatic Agents
/ therapeutic use
Biological Factors
/ therapeutic use
JAKi discontinuation
JAKi therapy
RA
efficacy
Journal
Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501
Informations de publication
Date de publication:
23 12 2022
23 12 2022
Historique:
received:
06
12
2021
revised:
29
04
2022
pubmed:
18
5
2022
medline:
28
12
2022
entrez:
17
5
2022
Statut:
ppublish
Résumé
JAK Inhibitors (JAKi) are recommended DMARDs for patients with moderate-to-severe RA who failed first-line therapy with methotrexate. There is a lack of data allowing an evidence-based choice of subsequent DMARD therapy for patients who had discontinued JAKi treatment. We aimed to compare the effectiveness of TNF inhibitor (TNFi) therapy vs JAKi vs other mode of action (OMA) biologic DMARD (bDMARD) in RA patients who were previously treated with a JAKi. RA patients who discontinued JAKi treatment within the Swiss RA registry SCQM were included for this observational prospective cohort study. The primary outcome was drug retention for either TNFi, OMA bDMARD or JAKi. The hazard ratio for treatment discontinuation was calculated adjusting for potential confounders. A descriptive analysis of the reasons for discontinuation was performed. Four hundred treatment courses of JAKi were included, with a subsequent switch to either JAKi, TNFi or OMA bDMARD. The crude overall drug retention was higher in patients switching to another JAKi as compared with TNFi and comparable to OMA. A significant difference of JAKi vs TNFi persisted after adjusting for potential confounders. In a real-world population of RA patients who discontinued treatment with a JAKi, switching to another JAKi resulted in a higher drug retention than switching to a TNFi. A switch to a second JAKi seems an effective therapeutic option.
Identifiants
pubmed: 35579338
pii: 6586789
doi: 10.1093/rheumatology/keac285
doi:
Substances chimiques
Janus Kinase Inhibitors
0
Tumor Necrosis Factor Inhibitors
0
Biological Products
0
Tumor Necrosis Factor-alpha
0
Antirheumatic Agents
0
Biological Factors
0
Types de publication
Observational Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
89-97Informations de copyright
© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.