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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

Authors
Park, Jeong-IkSong, Gi-WonRyu, Je HoChoi, Sang-TaeChoi, Nam-GyuJung, Bo-HyunChu, Chong WooKim, Keon-KukJung, Dong-HwanHa, Tae-YongMoon, Deok-BogYang, KwanghoShin, Min -HoChung, Yong-KyuHwang, ShinYoon, Young -InLee, Sung-Gyu
Issue Date
Mar-2023
Publisher
ELSEVIER SCIENCE INC
Citation
TRANSPLANTATION PROCEEDINGS, v.55, no.2, pp.387 - 395
Journal Title
TRANSPLANTATION PROCEEDINGS
Volume
55
Number
2
Start Page
387
End Page
395
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/88061
DOI
10.1016/j.transproceed.2023.01.013
ISSN
0041-1345
Abstract
Background. Mycophenolate mofetil exhibits pharmacologic mechanisms different from cal-cineurin 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).Methods. 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.Results. In the full analysis set population, the incidence of biopsy-proven acute cellular rejec-tion (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 recur-rence 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).Conclusion. 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 transplanta-tion in patients infected with HBV.
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