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Observational Study
. 2025 Jan 6;11(1):e005062.
doi: 10.1136/rmdopen-2024-005062.

Evaluation of rheumatoid arthritis-associated interstitial lung disease in patients treated with JAK inhibitors: a MAJIK-SFR cohort study

Affiliations
Observational Study

Evaluation of rheumatoid arthritis-associated interstitial lung disease in patients treated with JAK inhibitors: a MAJIK-SFR cohort study

Félicien Triboulet et al. RMD Open. .

Abstract

Objective: To examine the course of interstitial lung disease associated with rheumatoid arthritis (RA-ILD) in France on treatment with Janus kinase inhibitors (JAKis) using the MAJIK-SFR registry.

Methods: Prospective national multicentre observational study identifying patients with RA-ILD from the MAJIK-SFR registry. Pulmonary assessment data were collected at JAKi initiation and follow-up visits (6 months, 12 months and a median of 21 months postinclusion), including chest high-resolution CT (HRCT), pulmonary function tests (forced vital capacity (FVC) and diffusing capacity of the lungs for carbon monoxide (DLCO)), acute exacerbations of ILD, respiratory infections and lung cancers.

Results: We enrolled 42 patients (26 women, 62%) with RA-ILD with a mean age of 61±13 years and a mean disease duration of 16±10 years. Compared with the 778 RA patients without ILD from the MAJIK registry, RA-ILD patients were older, displayed more severe and active disease and had more prevalent comorbidities. Non-specific interstitial pneumonia and usual interstitial pneumonia accounted for 46% and 43% of the chest HRCT ILD patterns, respectively. No significant changes in FVC and DLCO were observed during the follow-up period. Chest HRCT lesions remained stable in 69% of patients. Progressive ILD was identified in 8 patients (19%). 16 (38%) respiratory tract infections were observed. Only one acute regressive exacerbation of ILD was noted, and no lung cancer was diagnosed. No deaths occurred. JAKi was discontinued in 17 patients including 8 for inefficacy on joint involvement and 5 for intolerance.

Conclusion: The analysis indicates stability of RA-ILD in patients treated with JAKi. The tolerance profile of JAKi in this higher risk population did not reveal new safety signal.

Keywords: Biological Therapy; Pulmonary Fibrosis; Rheumatoid Arthritis.

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Conflict of interest statement

Competing interests: JA: Honoraria: Galapagos, Alfasigma, Lilly, Pfizer, Abbvie, Bristol-Myers Squibb, Sanofi, Roche-Chugai, Nordic Pharma, Medac, Novartis, Biogen, Fresenius Kabi, Janssen and MSD. Research grants: Bristol-Myers Squibb, Pfizer (Passerelle), Novartis (Dreamer), Fresenius Kabi, Galapagos/Alfasigma, Nordic Pharma. M-ET and CP: Honoraria: Galapagos, Alfasigma, Lilly, Pfizer, Abbvie.

Figures

Figure 1
Figure 1. Flow chart of the study. ILD, interstitial lung disease; JAKi, Janus kinase inhibitor; RA, rheumatoid arthritis, COPD: chronic obstructive pulmonary disease.
Figure 2
Figure 2. Changes in FVC (A) and DLCO (B) during follow-up (median, 95% CI). DLCO, diffusing capacity of the lungs for carbon monoxide; FVC, forced vital capacity.

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