SAGE Open Medical Case Reports (Dec 2022)

Successful peficitinib addition on anti-MDA5 antibody-positive dermatomyositis refractory to triple therapy and glucocorticoid reduction

  • Yuki Oba,
  • Masayuki Yamanouchi,
  • Daisuke Ikuma,
  • Hiroki Mizuno,
  • Noriko Inoue,
  • Akinari Sekine,
  • Eiko Hasegawa,
  • Tatsuya Suwabe,
  • Naoki Sawa,
  • Yoshifumi Ubara

DOI
https://doi.org/10.1177/2050313X221141277
Journal volume & issue
Vol. 10

Abstract

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Anti-melanoma differentiation–associated gene 5 antibody-positive dermatomyositis is the poorest prognosis of all dermatomyositis due to its associated rapidly progressive interstitial lung disease. Intensive treatment is required from the onset and triple therapy with prednisolone, calcineurin inhibitors, and intravenous cyclophosphamide is recommended. However, some patients are refractory or dependent on this treatment and additional immunosuppressive therapy is required. Recently, the efficacy of tofacitinib, a JAK inhibitor, has been reported. Here, we describe a case of a 50-year-old woman with anti-melanoma differentiation–associated gene 5 antibody-positive dermatomyositis who became refractory to triple therapy and prednisolone reduction, and achieved remission with the addition of peficitinib, a JAK inhibitor. This is the first report showing that peficitinib is effective for anti-melanoma differentiation–associated gene 5 antibody-positive dermatomyositis and it may be a potential treatment option.