Successful peficitinib addition on anti-MDA5 antibody-positive dermatomyositis refractory to triple therapy and glucocorticoid reduction.
Yuki ObaMasayuki YamanouchiDaisuke IkumaHiroki MizunoNoriko InoueAkinari SekineEiko HasegawaTatsuya SuwabeNaoki SawaYoshifumi UbaraPublished in: SAGE open medical case reports (2022)
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.
Keyphrases
- interstitial lung disease
- systemic sclerosis
- rheumatoid arthritis
- disease activity
- idiopathic pulmonary fibrosis
- genome wide
- end stage renal disease
- systemic lupus erythematosus
- copy number
- high dose
- newly diagnosed
- risk assessment
- multiple sclerosis
- ejection fraction
- chronic kidney disease
- low dose
- dna methylation
- mesenchymal stem cells
- replacement therapy
- prognostic factors
- signaling pathway
- cell therapy
- cell death
- peritoneal dialysis
- ulcerative colitis
- breast cancer cells
- patient reported outcomes
- human health
- genome wide identification
- cell cycle arrest