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European journal of clinical pharmacology, 2024-04, Vol.80 (4), p.481-492
2024
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Autor(en) / Beteiligte
Titel
Tofacitinib for the treatment of severe rare skin diseases: a narrative review
Ist Teil von
  • European journal of clinical pharmacology, 2024-04, Vol.80 (4), p.481-492
Ort / Verlag
Berlin/Heidelberg: Springer Berlin Heidelberg
Erscheinungsjahr
2024
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Purpose Autoimmune bullous diseases, connective tissue diseases, and vasculitis represent a group of severe rare skin diseases. While glucocorticoids and immunosuppressive agents serve as standard treatments for these diseases, their efficacy is limited due to adverse side effects, indicating the need for alternative approaches. Biologics have been used in the management of some rare skin diseases. However, the use of biologics is associated with concerns, such as infection risk and high costs, prompting the quest for efficacious and cost-effective alternatives. This study discusses the safety issues associated with tofacitinib and its potential in treating rare skin diseases. Methods This narrative review focuses on the pharmacodynamic properties of tofacitinib and its impact on the JAK/STAT pathway. In addition, we present a comprehensive discussion of the effects and mechanism of action of tofacitinib for each severe rare skin disease. Results This role of tofacitinib in treating severe rare skin diseases has been discussed, shedding light on its promising prospects as a treatment modality. Few reports of serious adverse events are available in patients treated with tofacitinib. Conclusion We explored the mechanism of action, efficacy, and safety considerations of tofacitinib and found that it can be used as a treatment option for rare skin diseases. However, multicenter clinical studies are needed to confirm the efficacy and safety of JAK inhibitors.
Sprache
Englisch
Identifikatoren
ISSN: 0031-6970
eISSN: 1432-1041
DOI: 10.1007/s00228-024-03621-9
Titel-ID: cdi_proquest_miscellaneous_2915988940

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