Glucocorticoid sparing effect of Janus Kinase inhibitors compared to biological Disease Modifying Anti-Rheumatic Drugs in rheumatoid arthritis, a single-center retrospective analysis.

Baricitinib Filgotinib Glucocorticoid JAKi TNFi Tofacitinib Upadacitinib

Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
21 Aug 2024
Historique:
received: 18 04 2024
revised: 25 07 2024
accepted: 16 08 2024
medline: 21 8 2024
pubmed: 21 8 2024
entrez: 21 8 2024
Statut: aheadofprint

Résumé

Glucocorticoid sparing in rheumatoid arthritis (RA) treatment is crucial to minimizing adverse effects associated with long-term use. Janus kinase inhibitors (JAKi) could potentially offer a more potent glucocorticoid-sparing effect than biological Disease-Modifying Antirheumatic Drugs (bDMARDs). This is a single-center retrospective analysis of RA patients treated with JAKi or bDMARDs. Glucocorticoid tapering, rescue therapy and discontinuation were analyzed through mixed-effects models, Poisson regression, and multivariable logistic regression, respectively, adjusting for baseline disease activity, demographic factors, and treatment line. A total of 716 RA patients treated with JAKi (n = 156) or bDMARDs (n = 560) were evaluated. JAKi treatment was associated with a more rapid reduction in glucocorticoid dose within the first 6 months and 60% higher odds of discontinuation compared with bDMARDs (adjusted odds ratio 1.63, 95% CI 1.02-2.60, p 0.039). Despite a higher baseline glucocorticoid dose, over 50% of JAKi-treated patients discontinued glucocorticoids after 12 months, vs ∼40% for bDMARDs. The need for glucocorticoid rescue therapy was significantly higher in the bDMARD group (rate ratio 2.66 (95% CI, 1.88-3.74)). Our findings indicate that JAK inhibitors facilitate more rapid glucocorticoid tapering compared with bDMARDs in RA patients. These results underscore the potential of JAK inhibitors to reduce long-term glucocorticoid exposure, highlighting their value in RA management strategies, including minimizing glucocorticoid-related adverse effects.

Sections du résumé

BACKGROUND BACKGROUND
Glucocorticoid sparing in rheumatoid arthritis (RA) treatment is crucial to minimizing adverse effects associated with long-term use. Janus kinase inhibitors (JAKi) could potentially offer a more potent glucocorticoid-sparing effect than biological Disease-Modifying Antirheumatic Drugs (bDMARDs).
MATERIAL AND METHODS METHODS
This is a single-center retrospective analysis of RA patients treated with JAKi or bDMARDs. Glucocorticoid tapering, rescue therapy and discontinuation were analyzed through mixed-effects models, Poisson regression, and multivariable logistic regression, respectively, adjusting for baseline disease activity, demographic factors, and treatment line.
RESULTS RESULTS
A total of 716 RA patients treated with JAKi (n = 156) or bDMARDs (n = 560) were evaluated. JAKi treatment was associated with a more rapid reduction in glucocorticoid dose within the first 6 months and 60% higher odds of discontinuation compared with bDMARDs (adjusted odds ratio 1.63, 95% CI 1.02-2.60, p 0.039). Despite a higher baseline glucocorticoid dose, over 50% of JAKi-treated patients discontinued glucocorticoids after 12 months, vs ∼40% for bDMARDs. The need for glucocorticoid rescue therapy was significantly higher in the bDMARD group (rate ratio 2.66 (95% CI, 1.88-3.74)).
CONCLUSION CONCLUSIONS
Our findings indicate that JAK inhibitors facilitate more rapid glucocorticoid tapering compared with bDMARDs in RA patients. These results underscore the potential of JAK inhibitors to reduce long-term glucocorticoid exposure, highlighting their value in RA management strategies, including minimizing glucocorticoid-related adverse effects.

Identifiants

pubmed: 39167121
pii: 7738105
doi: 10.1093/rheumatology/keae455
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Giovanni Adami (G)

Rheumatology Unit, University of Verona, Verona, Italy.

Riccardo Bixio (R)

Rheumatology Unit, University of Verona, Verona, Italy.

Giulia Virelli (G)

Rheumatology Unit, University of Verona, Verona, Italy.

Isotta Galvagni (I)

Rheumatology Unit, University of Verona, Verona, Italy.

Francesca Mastropaolo (F)

Rheumatology Unit, University of Verona, Verona, Italy.

Andrea Morciano (A)

Rheumatology Unit, University of Verona, Verona, Italy.

Francesca Ruzzon (F)

Rheumatology Unit, University of Verona, Verona, Italy.

Valeria Messina (V)

Rheumatology Unit, University of Verona, Verona, Italy.

Elena Fracassi (E)

Rheumatology Unit, University of Verona, Verona, Italy.

Davide Gatti (D)

Rheumatology Unit, University of Verona, Verona, Italy.

Ombretta Viapiana (O)

Rheumatology Unit, University of Verona, Verona, Italy.

Antonio Carletto (A)

Rheumatology Unit, University of Verona, Verona, Italy.

Maurizio Rossini (M)

Rheumatology Unit, University of Verona, Verona, Italy.

Classifications MeSH