The Real-World Effectiveness, Persistence, Adherence, and Safety of Janus Kinase Inhibitor Baricitinib in Rheumatoid Arthritis: A Long-Term Study
-
Published:2024-04-25
Issue:9
Volume:13
Page:2517
-
ISSN:2077-0383
-
Container-title:Journal of Clinical Medicine
-
language:en
-
Short-container-title:JCM
Author:
Calvo-Garcia Alberto1ORCID, Ramírez Herráiz Esther1ORCID, Llorente Cubas Irene María2, Varas De Dios Blanca3ORCID, Benedí González Juana4, Morell Baladrón Alberto1, García-Vicuña Rosario25ORCID
Affiliation:
1. Pharmacy Service, Hospital Universitario La Princesa, IIS-Princesa, 28006 Madrid, Spain 2. Rheumatology Service, Hospital Universitario La Princesa, IIS-Princesa, 28006 Madrid, Spain 3. Rheumatology Service, Hospital Universitario Santa Cristina, 28006 Madrid, Spain 4. Pharmacology, Pharmacognosy and Botany Department, Pharmacy Faculty, Complutense University of Madrid, 28040 Madrid, Spain 5. Department of Medicine, Faculty of Medicine, Autonomous University of Madrid, 28049 Madrid, Spain
Abstract
Background/Aim: Baricitinib (BAR) is the first oral selective Janus kinase inhibitor approved in Europe for rheumatoid arthritis (RA). Real-world data are still needed to clarify its long-term benefits/risk profile. This study aimed to evaluate the effectiveness, persistence, adherence, and safety of BAR in a real-world setting. Methods: An ambispective study was conducted between October 2017 and December 2021 in RA patients starting BAR. The effectiveness was evaluated, assessing changes from the baseline of the Disease Activity Score using 28-joint counts-C reactive protein (DAS28CRP), and the achievement of low disease activity/remission. Drug persistence was evaluated using Kaplan–Meier analysis. Adherence was estimated using the medication possession ratio (MPR) and the 5-item Compliance Questionnaire for Rheumatology. Safety was assessed determining global incidence proportion and adverse event adjusted incidence rates. Results: In total, 61/64 recruited patients were finally analyzed, 83.6% were female, 78.7% were seropositive, the mean age was 58.1 (15.4) years, and the disease duration was 13.9 (8.3) years. A total of 32.8% of patients were naïve to biologics and 16.4% received BAR as monotherapy. The median exposure to BAR was 12.4 (6.6–31.2) months (range 3.1–51.4). A significant change in DAS28CRP was observed after treatment (difference −1.2, p = 0.000). 70.5% and 60.7% of patients achieved low disease activity or remission, respectively, and 50.8% (31/61) remained on BAR throughout the follow-up, with a median persistence of 31.2 (9.3–53.1) months. The average MPR was 0.96 (0.08) and all patients exhibited “good adherence” according to the questionnaire. In total, 21.3% of patients discontinued baricitinib due to toxicity. Conclusions: In our real-world practice, BAR demonstrated effectiveness, large persistence, high adherence to treatment, and an acceptable safety profile.
Reference59 articles.
1. Diagnosis and Management of Rheumatoid Arthritis: A Review;Aletaha;JAMA,2018 2. Immunopathogenesis of rheumatoid arthritis;Firestein;Immunity,2017 3. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update;Smolen;Ann. Rheum. Dis.,2023 4. Taylor, P.C., Laedermann, C., Alten, R., Feist, E., Choy, E., Haladyj, E., De La Torre, I., Richette, P., Finckh, A., and Tanaka, Y. (2023). A JAK Inhibitor for Treatment of Rheumatoid Arthritis: The Baricitinib Experience. J. Clin. Med., 12. 5. Baricitinib, Methotrexate, or Combination in Patients with RA and No or Limited Prior DMARDs Treatment;Fleischmann;Arthritis Rheumatol.,2017
|
|