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Tracheobronchial Stenosis in Granulomatosis with Polyangiitis: Immunosuppressant Use and Airway Dilation Frequency

Denvir, B.; Shah, A. A.; Hillel, A. T.; Seo, P.; Kim, J. S.; Antiochos, B.

2025-07-25 rheumatology
10.1101/2025.07.25.25332215 medRxiv
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ObjectiveTracheobronchial stenosis (TBS) occurs in 13-27% of patients with granulomatosis with polyangiitis (GPA) and may cause life-threatening airway compromise. Despite advances in treatment, TBS remains difficult to manage, with frequent relapses and high procedural burden. The objective of this study was to evaluate the relationship between immunosuppressant use and frequency of relapse in patients with TBS-GPA. MethodsWe performed retrospective review of patients with TBS-GPA seen at Johns Hopkins Medical Institutions between 2013-2024. Baseline demographic and clinical characteristics, immunosuppressant exposure, and tracheal dilation procedure dates were abstracted. A multivariate mixed effects Poisson regression model was used to assess the association between immunosuppressant exposures (rituximab, cyclophosphamide, methotrexate, azathioprine, leflunomide, and mycophenolate) and tracheal dilation incidence, adjusting for age, years since TBS diagnosis, anti-neutrophil cytoplasmic antibody (ANCA) status, GPA disease severity, and concomitant treatment with glucocorticoid injections. ResultsA total of 56 patients with TBS-GPA were included in the analysis, with a mean follow-up duration of 9.9 years. In the adjusted mixed-effects Poisson model, patient-years on leflunomide were associated with a 64% lower incidence of tracheal dilations compared to periods off leflunomide (IRR 0.36, p = 0.002). No statistically significant associations were observed for the other immunosuppressants measured. Among other tested covariates, age under 40, severe GPA, and concomitant glucocorticoid injections were associated with higher dilation frequency. ConclusionLeflunomide use was associated with a lower frequency of tracheal dilations in patients with TBS-GPA. These findings support the need for further evaluation of leflunomide as a treatment option in this population.

Published in ACR Open Rheumatology · not in our set (fewer than 10 published preprints to learn from) · training set

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