The Retention Rate and Safety of JAK Inhibitors in Rheumatoid Arthritis: Real Word Data from a Monocentric Cohort

Author:

Donzella Denise1ORCID,Bellis Elisa1ORCID,Crepaldi Gloria1,Data Valeria1,Gatto Mariele1ORCID,Lomater Claudia1,Liperoti Gaetano1,Marucco Elena1,Saracco Marta1,Iagnocco Annamaria1

Affiliation:

1. Academic Rheumatology Centre, Ospedale Mauriziano—Clinical and Biological Sciences Department, University of Turin, 10024 Turin, Italy

Abstract

Background/Objectives: To date, the literature concerning real-world data on the retention rate and safety of Janus kinase inhibitors (JAKis) is limited. To retrospectively evaluate the overall drug retention rate (DRR) of different JAKis in a monocentric cohort of patients with rheumatoid arthritis (RA). Methods: Patients diagnosed with RA and treated with JAKis who were evaluated at our outpatient clinic from March 2017 to December 2023 were included in the study. Demographic, clinical characteristics, and comorbidities were recorded. The DRR was evaluated as the time to drug discontinuation, and baseline predictors of drug discontinuation were investigated through Cox regression after adjusting for baseline confounders. Results: The global DRR for JAKis was 51.3%. The DRR was 37.5% for tofacitinib, 46.6% for baricitinib, 69.4% for upadacitinib, and 53.5% for filgotinib. Considering all JAKis, the only significant predictor of drug discontinuation was the use of JAKis as a first-line treatment (HR 95% CI [0.25 (0.13–0.46)]. When considering each JAKi individually, a longer disease duration predicted TOF discontinuation (HR95% CI [1.05 (1.01–1.09)], while seropositivity protected against TOF being withdrawn (HR95% CI [0.41 (0.17–0.97)]. No independent predictors emerged for other JAKis. Conclusions: the use of JAKis as a first-line treatment as well as disease duration and serology may impact the DRR of JAKis, which may inform tailored treatment strategies in clinical practice.

Publisher

MDPI AG

Reference13 articles.

1. Rheumatoid Arthritis—Common Origins, Divergent Mechanisms;Gravallese;N. Engl. J. Med.,2023

2. Janus Kinase-Targeting Therapies in Rheumatology: A Mechanisms-Based Approach;Tanaka;Nat. Rev. Rheumatol.,2022

3. EULAR Recommendations for the Management of Rheumatoid Arthritis with Synthetic and Biological Disease-Modifying Antirheumatic Drugs: 2019 Update;Smolen;Ann. Rheum. Dis.,2020

4. Oral Surveillance and JAK Inhibitor Safety: The Theory of Relativity;Winthrop;Nat. Rev. Rheumatol.,2022

5. European Medicines Agency—EMA (2024, March 03). EMA Confirms Measures to Minimise Risk of Serious Side Effects with Janus Kinase Inhibitors for Chronic Inflammatory Disorders. EMA/142279/2023. Available online: https://www.ema.europa.eu/en/documents/referral/janus-kinase-inhibitors-jaki-article-20-procedure-ema-confirms-measures-minimise-risk-serious-side-effects-janus-kinase-inhibitors-chronic-inflammatory-disorders_en.pdf-0.

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