Tofacitinib as a Steroid-Sparing Therapy in Pulmonary Sarcoidosis, an Open-Label Prospective Proof-of-Concept Study

This is a prospective, open-label, proof-of-concept study of tofacitinib, a Janus kinase inhibitor, as a steroid-sparing therapy in corticosteroid-dependent pulmonary sarcoidosis. Five patients with corticosteroid-dependent pulmonary sarcoidosis were treated with tofacitinib 5 mg twice daily. The pr...

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Published inLung Vol. 199; no. 2; pp. 147 - 153
Main Authors Friedman, Marcia A., Le, Brian, Stevens, Janelle, Desmarais, Julianna, Seifer, Daniel, Ogle, Kimberly, Choi, Dongseok, Harrington, Christina A., Jackson, Peter, Rosenbaum, James T.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.04.2021
Springer
Springer Nature B.V
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Summary:This is a prospective, open-label, proof-of-concept study of tofacitinib, a Janus kinase inhibitor, as a steroid-sparing therapy in corticosteroid-dependent pulmonary sarcoidosis. Five patients with corticosteroid-dependent pulmonary sarcoidosis were treated with tofacitinib 5 mg twice daily. The primary endpoint was a ≥ 50% reduction in corticosteroids at week 16 with no worsening in pulmonary function or respiratory symptoms. 60% of patients (3/5) met the primary endpoint. One patient was lost to follow up prior to steroid taper, and another was withdrawn due to worsening of known neurosarcoidosis. The three patients who met the primary endpoint each tapered to ≤ 5 mg/day prednisone, respiratory symptoms improved, and spirometry remained stable. In this proof-of-concept study, the addition of a JAK-inhibitor allowed 60% of patients with pulmonary sarcoidosis to successfully taper corticosteroids. JAK-inhibitors are a promising therapy for pulmonary sarcoidosis, which require further investigation in randomized trials. Trial Registration clinicaltrials.gov NCT03793439; registered Jan 4, 2019.
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Authors’ contributions: JTR conceived of the study. JTR, MAF, JS, KO, and PJ designed the study. MAF, BL, KO, JD, DS, and JTR collected the clinical data. JTR, MAF, JS, PJ, MAF, BL, JD, and DS analyzed the clinical data. CH extracted RNA and performed RNA sequencing. DC analyzed transcriptomic data. MAF and BL wrote the first draft of the manuscript. All authors substantially contributed to this work, all authors critically revised this manuscript for important intellectual contact, all authors approve the version to be publish, and all authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated.
ISSN:0341-2040
1432-1750
DOI:10.1007/s00408-021-00436-8