Chinese Hepatolgy ›› 2025, Vol. 30 ›› Issue (2): 240-244.

• Other Ljiver Diseases • Previous Articles     Next Articles

Rucotinib combined with artificial liver for severe hepatic graft-versus-host disease with poor glucocorticoid response:A report of 3 cases

ZHOU Xing-nian, ZHAO Peng, GAO Ting, ZHANG Quan, LI Hong   

  1. 1. The Affiliated Hospital of Guizhou Medical University, Guiyang 550001, China;
    2. Guizhou Provincial People's Hospital, Guiyang 550001, China
  • Received:2023-12-25 Online:2025-02-28 Published:2025-03-17
  • Contact: LI Hong, Email:625062102@qq.com

Abstract: Objective To observe the efficacy of Rucotinib combined with artificial liver in the treatment of 3 cases of severe liver graft-versus-host disease(GVHD) with poor glucocorticoid response. Methods A total of 3 patients with severe liver graft-versus-host disease after allogeneic hematopoietic stem cell transplantation were retrospectively collected from January 2017 to December 2021 in the Infectious disease Department of Affiliated Hospital of Guizhou Medical University. All 3 patients were treated with Rucotinib combined with artificial liver, and received active infection prevention and symptomatic treatment. Results Three patients with severe liver GVHD were treated with Rucotinib combined with artificial liver PE and DPMAS, and the liver function was significantly improved and the prognosis was favorable. Conclusion The prognosis of liver graft-versus-host disease is poor, and early diagnosis and treatment are essential. The abnormal elevation of ALP and glutamyltranspeptide before total bilirubin after allogeneic hematopoietic stem cell transplantation may serve as an important early warning indicator of chronic liver GVHD. Early treatment with rucotinib can improve the over-activation of immune system, reduce the damage of bile duct epithelial cells, thereby reducing liver damage, avoiding artificial liver treatment, and prolonging the survival time of patients.

Key words: Ruxolitinib, Artificial liver, Glucocorticoid, Graft versus host disease