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Efficacy and safety of prolonged-release versus immediate-release tacrolimus in de novo liver transplant recipients in South Korea: A randomized open-label phase 4 study (MAPLE)open access

Authors
Kim, Myoung SooJoh, Jae-WonKim, Dong-SikKim, Seoung HoonChoi, Jin SubLee, JaegeunLee, Jee YounKim, Jong ManKwon, Choon Hyuck DavidChoi, Gyu-SeongYu, Young DongYoon, Yong-InHan, Jae HyunLee, Yun JeongJiang, HongsiKim, Soon-Il
Issue Date
Jun-2019
Publisher
Korean Society for Transplantation
Keywords
Humans; Immunosuppressive agents; Liver transplantation; Prolonged-release tacrolimus; Republic of Korea; Treatment outcome
Citation
Korean Journal of Transplantation, v.33, no.2, pp 20 - 29
Pages
10
Indexed
SCOPUS
KCI
Journal Title
Korean Journal of Transplantation
Volume
33
Number
2
Start Page
20
End Page
29
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/65270
DOI
10.4285/jkstn.2019.33.2.20
ISSN
2671-8790
Abstract
Background: Prolonged-release tacrolimus is associated with better long-term graft and patient survival than the immediate-release formulation in liver transplant patients. However, no clinical data are available to assess the efficacy and safety of early conversion from twice-daily, immediate-release tacrolimus to once-daily, prolonged-release tacrolimus in de novo liver transplant recipients in Korea. Methods: A 24-week, randomized, open-label study was conducted in 36 liver transplant recipients. All patients received immediaterelease tacrolimus (0.1-0.2 mg/kg/day, divided into two doses) for 4 weeks after transplantation, at which time 50% of the patients were converted, at a ratio of 1 mg to 1 mg, to prolonged-release tacrolimus (once-daily). The primary efficacy endpoint was the incidence of biopsy-confirmed acute rejection (BCAR) from weeks 4 to 24 after transplantation (per-protocol set). Medication adherence, adverse event profiles, laboratory tests, vital signs, and physical changes were also recorded. Results: BCAR frequency at 24 weeks was similar between the two treatment groups; two cases (mean±standard deviation, 0.14±0.53 cases) of BCAR were reported in one patient treated with prolonged-release tacrolimus (n=14), while no such cases were reported among patients treated with immediate-release tacrolimus (n=12). The tacrolimus blood concentration at weeks 12 and 24, medication adherence, and adverse event profiles were also similar between the formulations, with no unusual laboratory test results, vital signs, or physical changes reported. Conclusions: Early conversion to a simplified, once-daily, prolonged-release tacrolimus regimen may be an effective treatment option for liver transplant recipients in Korea. Larger-scale studies are warranted to confirm non-inferiority to immediate-release tacrolimus formulation in de novo liver transplant recipients. © 2021 Korean Journal of Transplantation. All rights reserved.
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Anam Hospital (Department of Hepato-Biliary-Pancreatic Surgery, Anam Hospital)
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