One-Year Medication Adherence and Persistence in Rheumatoid Arthritis in Clinical Practice: A Retrospective Analysis of Upadacitinib, Adalimumab, Baricitinib, and Tofacitinib.

Discontinuation Janus kinase inhibitor Medication adherence Real-world Rheumatoid arthritis Treatment persistence Tumor necrosis factor inhibitor Upadacitinib

Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
10 2023
Historique:
received: 06 04 2023
accepted: 17 07 2023
medline: 14 9 2023
pubmed: 6 8 2023
entrez: 5 8 2023
Statut: ppublish

Résumé

This study evaluated 12 months adherence and persistence among Janus kinase inhibitors (upadacitinib, baricitinib, tofacitinib) and adalimumab, a tumor necrosis factor inhibitor (TNFi), in patients with rheumatoid arthritis (RA). This retrospective analysis used administrative claims data from the Merative™ MarketScan In total, 6317 patients were included (683 upadacitinib, 3732 adalimumab, 132 baricitinib, 1770 tofacitinib). Compared with upadacitinib, patients initiating adalimumab [aOR (95% CI): 0.82 (0.69, 0.96)], baricitinib [0.46 (0.31, 0.68)], and tofacitinib [0.74 (0.62, 0.88)] were significantly less likely to achieve PDC ≥ 80%. Risk of treatment discontinuation was significantly higher in patients treated with adalimumab [aHR (95% CI): 1.14 (1.01, 1.29)], baricitinib [1.48 (1.16, 1.90)], and tofacitinib [1.22 (1.07, 1.38)] compared with upadacitinib. Mean time to discontinuation was 256 (upadacitinib), 249 (adalimumab), 221 (baricitinib), and 239 (tofacitinib) days. Similar results were observed in patients with prior TNFi use. Patients with RA, regardless of recent TNFi experience, initiating upadacitinib were significantly more likely to be adherent and less likely to discontinue therapy compared to adalimumab, baricitinib, and tofacitinib in the first 12 months of treatment.

Identifiants

pubmed: 37542646
doi: 10.1007/s12325-023-02619-6
pii: 10.1007/s12325-023-02619-6
pmc: PMC10499920
doi:

Substances chimiques

Adalimumab FYS6T7F842
tofacitinib 87LA6FU830
Antirheumatic Agents 0
upadacitinib 4RA0KN46E0
baricitinib ISP4442I3Y

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

4493-4503

Informations de copyright

© 2023. The Author(s).

Références

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Auteurs

Martin Bergman (M)

College of Medicine, Drexel University, Philadelphia, PA, USA.

Naijun Chen (N)

AbbVie Inc., 26525 N Riverwoods Blvd., Mettawa, North Chicago, IL, 60045, USA.

Richard Thielen (R)

AbbVie Inc., 26525 N Riverwoods Blvd., Mettawa, North Chicago, IL, 60045, USA.

Patrick Zueger (P)

AbbVie Inc., 26525 N Riverwoods Blvd., Mettawa, North Chicago, IL, 60045, USA. patrick.zueger@abbvie.com.

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Classifications MeSH