A Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Tacrolimus and Corticosteroids in Combination With or Without Mycophenolate Mofetil in Liver Transplantation Recipients Infected With Hepatitis B Virus

医学 他克莫司 养生 免疫抑制 肝移植 人口 内科学 钙调神经磷酸酶 胃肠病学 移植 不利影响 外科 免疫学 环境卫生
作者
Jeong-Ik Park,Gi‐Won Song,Je Ho Ryu,Sang-Tae Choi,Nam-Gyu Choi,Bo‐Hyun Jung,Chong Woo Chu,Keon-Kuk Kim,Dong‐Hwan Jung,Tae‐Yong Ha,Deok‐Bog Moon,Kwangho Yang,Min‐Ho Shin,Yong‐Kyu Chung,Shin Hwang,Young‐In Yoon,Sung‐Gyu Lee
出处
期刊:Transplantation Proceedings [Elsevier BV]
卷期号:55 (2): 387-395 被引量:2
标识
DOI:10.1016/j.transproceed.2023.01.013
摘要

Mycophenolate mofetil exhibits pharmacologic mechanisms different from calcineurin inhibitors. Therefore, the dose of calcineurin inhibitors can be reduced along with side effects for effective immunosuppression. We aimed to evaluate the efficacy and safety of tacrolimus and corticosteroid in combination with or without mycophenolate mofetil in living donor liver transplantation (LDLT) recipients infected with hepatitis B virus (HBV). A randomized, open-label, comparative, multicenter, phase IV study was conducted with 119 patients from January 2014 to September 2017. In the full analysis set population, 58 and 59 patients were included in the study group (triple-drug regimen: TacroBell + My-rept + corticosteroid) and the control group (dual-drug regimen: TacroBell + corticosteroid), respectively. In the per protocol set population, 49 and 42 patients were included in the study and control groups, respectively. In the full analysis set population, the incidence of biopsy-proven acute cellular rejection (rejection activity index score ≥4) was 3.4% in the study group; however, this finding was not observed in the control group (P = .468). Hepatitis B virus recurrence was observed in one patient in the control group. No cases of biopsy-proven acute cellular rejection and HBV recurrence were observed in the per protocol set population. The incidences of serious adverse events were 25.9% and 18.0% in the study and control groups, respectively; however, the difference between the groups was not statistically significant (P = .376). Although the study involved a small number of patients, the triple-drug regimen can be considered safe and effective for immunosuppression after living donor liver transplantation in patients infected with HBV.
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