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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)
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-relea...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Transplantation
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186832/ https://www.ncbi.nlm.nih.gov/pubmed/35769149 http://dx.doi.org/10.4285/jkstn.2019.33.2.20 |
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author | Kim, Myoung Soo Joh, Jae-Won Kim, Dong-Sik Kim, Seoung Hoon Choi, Jin Sub Lee, Jaegeun Lee, Jee Youn Kim, Jong Man Kwon, Choon Hyuck David Choi, Gyu-Seong Yu, Young Dong Yoon, Yong-In Han, Jae Hyun Lee, Yun Jeong Jiang, Hongsi Kim, Soon-Il |
author_facet | Kim, Myoung Soo Joh, Jae-Won Kim, Dong-Sik Kim, Seoung Hoon Choi, Jin Sub Lee, Jaegeun Lee, Jee Youn Kim, Jong Man Kwon, Choon Hyuck David Choi, Gyu-Seong Yu, Young Dong Yoon, Yong-In Han, Jae Hyun Lee, Yun Jeong Jiang, Hongsi Kim, Soon-Il |
author_sort | Kim, Myoung Soo |
collection | PubMed |
description | 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 immediate- release 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. |
format | Online Article Text |
id | pubmed-9186832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Society for Transplantation |
record_format | MEDLINE/PubMed |
spelling | pubmed-91868322022-06-28 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) Kim, Myoung Soo Joh, Jae-Won Kim, Dong-Sik Kim, Seoung Hoon Choi, Jin Sub Lee, Jaegeun Lee, Jee Youn Kim, Jong Man Kwon, Choon Hyuck David Choi, Gyu-Seong Yu, Young Dong Yoon, Yong-In Han, Jae Hyun Lee, Yun Jeong Jiang, Hongsi Kim, Soon-Il Korean J Transplant Original Article 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 immediate- release 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. The Korean Society for Transplantation 2019-06-30 2019-06-30 /pmc/articles/PMC9186832/ /pubmed/35769149 http://dx.doi.org/10.4285/jkstn.2019.33.2.20 Text en © 2019 The Korean Society for Transplantation https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Myoung Soo Joh, Jae-Won Kim, Dong-Sik Kim, Seoung Hoon Choi, Jin Sub Lee, Jaegeun Lee, Jee Youn Kim, Jong Man Kwon, Choon Hyuck David Choi, Gyu-Seong Yu, Young Dong Yoon, Yong-In Han, Jae Hyun Lee, Yun Jeong Jiang, Hongsi Kim, Soon-Il 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) |
title | 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) |
title_full | 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) |
title_fullStr | 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) |
title_full_unstemmed | 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) |
title_short | 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) |
title_sort | 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) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186832/ https://www.ncbi.nlm.nih.gov/pubmed/35769149 http://dx.doi.org/10.4285/jkstn.2019.33.2.20 |
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