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Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction

Calcineurin inhibitors (CNIs) are frequently given at a reduced dose in combination with mycophenolate mofetil (MMF) to avoid nephrotoxicity, but the optimal reduction in CNI dose has not been established. In this prospective, open-label, multicenter study, liver transplant recipients with chronic r...

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Autores principales: Wang, Pusen, Que, Weitao, Li, Hao, Yan, Lvnan, Fu, Zhiren, Ye, Qifa, Chen, Guihua, Dou, Kefeng, Lu, Shichun, Yang, Zhanyu, Zhu, Zhijun, Peng, Zhihai, Zhong, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593662/
https://www.ncbi.nlm.nih.gov/pubmed/28915690
http://dx.doi.org/10.18632/oncotarget.15490
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author Wang, Pusen
Que, Weitao
Li, Hao
Yan, Lvnan
Fu, Zhiren
Ye, Qifa
Chen, Guihua
Dou, Kefeng
Lu, Shichun
Yang, Zhanyu
Zhu, Zhijun
Peng, Zhihai
Zhong, Lin
author_facet Wang, Pusen
Que, Weitao
Li, Hao
Yan, Lvnan
Fu, Zhiren
Ye, Qifa
Chen, Guihua
Dou, Kefeng
Lu, Shichun
Yang, Zhanyu
Zhu, Zhijun
Peng, Zhihai
Zhong, Lin
author_sort Wang, Pusen
collection PubMed
description Calcineurin inhibitors (CNIs) are frequently given at a reduced dose in combination with mycophenolate mofetil (MMF) to avoid nephrotoxicity, but the optimal reduction in CNI dose has not been established. In this prospective, open-label, multicenter study, liver transplant recipients with chronic renal dysfunction who were administered a CNI-based immunosuppressive regimen were included in the intent-to-treat (ITT) population. The primary endpoint was declination in renal function, which was defined as a ≥ 20% decrease in the glomerular filtration rate during the year following regimen adjustment. In the ITT population, renal function declined after regimen adjustment in three patients (7%) in the MMF plus 50% CNI reduction group. Additionally, three of 40 patients (7.5%) in the MMF plus 75% CNI reduction group experienced at least one clinically suspected or biopsy-proven acute rejection. There were no differences between the two groups. The corrected mean improvement in creatinine clearance at week 52 was 6.551 mL/min in the MMF plus 50% CNI reduction group and 6.442 mL/min in the MMF plus at least 75% CNI reduction group. Thus, a regimen of MMF combined with a 50% or at least 70% reduction in CNI dose could improve renal function and was both tolerable and safe.
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spelling pubmed-55936622017-09-14 Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction Wang, Pusen Que, Weitao Li, Hao Yan, Lvnan Fu, Zhiren Ye, Qifa Chen, Guihua Dou, Kefeng Lu, Shichun Yang, Zhanyu Zhu, Zhijun Peng, Zhihai Zhong, Lin Oncotarget Clinical Research Paper Calcineurin inhibitors (CNIs) are frequently given at a reduced dose in combination with mycophenolate mofetil (MMF) to avoid nephrotoxicity, but the optimal reduction in CNI dose has not been established. In this prospective, open-label, multicenter study, liver transplant recipients with chronic renal dysfunction who were administered a CNI-based immunosuppressive regimen were included in the intent-to-treat (ITT) population. The primary endpoint was declination in renal function, which was defined as a ≥ 20% decrease in the glomerular filtration rate during the year following regimen adjustment. In the ITT population, renal function declined after regimen adjustment in three patients (7%) in the MMF plus 50% CNI reduction group. Additionally, three of 40 patients (7.5%) in the MMF plus 75% CNI reduction group experienced at least one clinically suspected or biopsy-proven acute rejection. There were no differences between the two groups. The corrected mean improvement in creatinine clearance at week 52 was 6.551 mL/min in the MMF plus 50% CNI reduction group and 6.442 mL/min in the MMF plus at least 75% CNI reduction group. Thus, a regimen of MMF combined with a 50% or at least 70% reduction in CNI dose could improve renal function and was both tolerable and safe. Impact Journals LLC 2017-02-18 /pmc/articles/PMC5593662/ /pubmed/28915690 http://dx.doi.org/10.18632/oncotarget.15490 Text en Copyright: © 2017 Wang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Clinical Research Paper
Wang, Pusen
Que, Weitao
Li, Hao
Yan, Lvnan
Fu, Zhiren
Ye, Qifa
Chen, Guihua
Dou, Kefeng
Lu, Shichun
Yang, Zhanyu
Zhu, Zhijun
Peng, Zhihai
Zhong, Lin
Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title_full Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title_fullStr Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title_full_unstemmed Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title_short Efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
title_sort efficacy and safety of a reduced calcineurin inhibitor dose combined with mycophenolate mofetil in liver transplant patients with chronic renal dysfunction
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593662/
https://www.ncbi.nlm.nih.gov/pubmed/28915690
http://dx.doi.org/10.18632/oncotarget.15490
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