Study of Tofacitinib in Refractory Dermatomyositis: An Open‐Label Pilot Study of Ten Patients

• Published in: Arthritis & rheumatology (Hoboken, N.J.) Vol. 73; no. 5; pp. 858 - 865
• Main Authors: Paik, Julie J., Casciola‐Rosen, Livia, Shin, Joseph Yusup, Albayda, Jemima, Tiniakou, Eleni, Leung, Doris G., Gutierrez‐Alamillo, Laura, Perin, Jamie, Florea, Liliana, Antonescu, Corina, Leung, Sherry G., Purwin, Grazyna, Koenig, Andrew, Christopher‐Stine, Lisa
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.05.2021
• Subjects: Adult; Biopsy; Chemokine CXCL10 - metabolism; Chemokine CXCL9 - metabolism; Chemokines; Clinical trials; Creatine; Creatine kinase; Criteria; CXCL10 protein; Dermatomyositis; Dermatomyositis - drug therapy; Dermatomyositis - metabolism; Dermatomyositis - physiopathology; Female; Gene expression; Gene sequencing; Health services; Humans; Immunohistochemistry; Inflammatory diseases; Interferon; Janus Kinase Inhibitors - therapeutic use; Kinases; Male; Middle Aged; Muscle, Skeletal - metabolism; Musculoskeletal diseases; Myositis; Pilot Projects; Piperidines - therapeutic use; Proof of Concept Study; Prospective Studies; Pyrimidines - therapeutic use; RNA-Seq; Safety; Sequence analysis; Skin - metabolism; Stat1 protein; STAT1 Transcription Factor - metabolism; Statistical analysis; Statistical methods; Treatment Outcome
• DOI: 10.1002/art.41602
• ISSN: 2326-5191; 2326-5205

Objective This open‐label 12‐week study was conducted to evaluate the efficacy and safety of tofacitinib, a JAK inhibitor, in treatment‐refractory active dermatomyositis (DM). Methods Tofacitinib in extended‐release doses of 11 mg was administered daily to 10 subjects with DM. Prior to treatment, a complete washout of all steroid‐sparing agents was performed. The primary outcome measure was assessment of disease activity improvement based on the International Myositis Assessment and Clinical Studies group definition of improvement. Response rate was measured as the total improvement score according to the 2016 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) myositis response criteria. Secondary outcome measures included Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI) scores, chemokine levels, immunohistochemical analysis of STAT1 expression in the skin, RNA sequencing analysis, and safety. Results At 12 weeks, the primary outcome was met in all 10 subjects. Five (50%) of 10 subjects experienced moderate improvement in disease activity, and the other 50% experienced minimal improvement according to the 2016 ACR/EULAR myositis response criteria. The secondary outcome of the mean change in the CDASI activity score over 12 weeks was statistically significant (mean ± SD 28 ± 15.4 at baseline versus 9.5 ± 8.5 at 12 weeks) (P = 0.0005). Serum chemokine levels of CXCL9/CXCL10 showed a statistically significant change from baseline. A marked decrease in STAT1 signaling in association with suppression of interferon target gene expression was demonstrated in 3 of 9 skin biopsy samples from subjects with dermatomyositis. The mean ± SD level of creatine kinase in the 10 subjects at baseline was 82 ± 34.8 IU/liter, highlighting that disease activity was predominantly located in the skin. Conclusion This is the first prospective, open‐label clinical trial of tofacitinib in DM that demonstrates strong clinical efficacy of a pan‐JAK inhibitor, as measured by validated myositis response criteria. Future randomized controlled trials using JAK inhibitors should be considered for treating DM.