[Importance of mycophenolate mofetil for treatment of interstitial lung disease in systemic sclerosis].
Udo SchneiderElise SiegertSven GläserKlaus Krügernull nullAndreas KrausePublished in: Zeitschrift fur Rheumatologie (2021)
Interstitial lung disease in systemic sclerosis (SSc-ILD) is a frequent organ complication with considerable mortality. Therapeutically, immunosuppressants are primarily used, particularly cyclophosphamide (CYC) and mycophenolate mofetil (MMF). Recently acquired data also showed an efficacy of the biologics rituximab and tocilizumab. The therapeutic options have most recently been expanded by the approval of the antifibrotic drug nintedanib. It is particularly beneficial in progressive fibrosing courses of ILD despite immunosuppression. The data from controlled trials on the efficacy and safety of CYC and MMF compiled in this review argue for a preferential use of MMF; however, the approval of MMF for this indication is still lacking. This is urgently needed for improved and simplified care of patients with SSc-ILD.
Keyphrases
- interstitial lung disease
- systemic sclerosis
- rheumatoid arthritis
- electronic health record
- healthcare
- idiopathic pulmonary fibrosis
- big data
- multiple sclerosis
- low dose
- palliative care
- drug administration
- diffuse large b cell lymphoma
- cardiovascular events
- high dose
- risk factors
- quality improvement
- machine learning
- juvenile idiopathic arthritis
- data analysis
- adverse drug
- chronic pain
- replacement therapy