Literature DB >> 28810721

De novo low-dose sirolimus versus mycophenolate mofetil in combination with extended-release tacrolimus in kidney transplant recipients: a multicentre, open-label, randomized, controlled, non-inferiority trial.

Kyu Ha Huh1,2, Jae Geun Lee1, Jongwon Ha3, Chang-Kwon Oh4, Man Ki Ju2,5, Chan-Duck Kim6, Hong Rae Cho7, Cheol Woong Jung8, Beom Jin Lim9, Yu Seun Kim1,2.   

Abstract

BACKGROUND: Most of the previous studies reported that tacrolimus (TAC) with sirolimus (SRL) was associated with worse post-transplant outcomes in kidney transplantation, compared with TAC with mycophenolate mofetil (MMF). These might be attributable to high-dose SRL. However, outcomes using low-dose SRL with TAC for kidney transplantation are uncertain. The aim of this study was to assess the efficacy and safety of low-dose SRL with extended-release tacrolimus (ER-TAC) versus MMF with ER-TAC.
METHODS: We randomly assigned 158 renal transplant patients to receive low-dose SRL or MMF in combination with ER-TAC and corticosteroid. The primary endpoint was the composite efficacy failure rate, including biopsy-proven acute rejection (BPAR), graft loss, death or loss to follow-up, within 12 months post-transplantation. This trial is registered with ClinicalTrial.gov (number NCT01680952).
RESULTS: The efficacy failure rate was 6.6% in the low-dose SRL group and 13.3% in the MMF group in the intention-to-treat population (absolute difference, 6.8%; 95% confidence interval, -2.8% to 16.3%). The incidence of BPAR within 12 months post-transplantation was 5.3% in the low-dose SRL group and 13.3% in the MMF group (P = 0.09). The mean estimated glomerular filtration rate at 12 months post-transplantation was 53.2 mL/min/1.73 m2 in the low-dose SRL group and 52.4 mL/min/1.73 m2 in the MMF group (P = 0.76). The incidences of adverse events and serious adverse events were similar between groups.
CONCLUSION: Low-dose SRL with ER-TAC was not inferior to MMF with ER-TAC with respect to efficacy and safety. When used for immunosuppression in kidney transplantation, low-dose SRL with ER-TAC can effectively prevent acute rejection and preserve renal function.
© The Author 2017. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Entities:  

Keywords:  kidney transplantation; mofetil; mycophenolate; post-transplant outcome; sirolimus; tacrolimus

Mesh:

Substances:

Year:  2017        PMID: 28810721     DOI: 10.1093/ndt/gfx093

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  5 in total

1.  Target of rapamycin inhibitors (TOR-I; sirolimus and everolimus) for primary immunosuppression in kidney transplant recipients.

Authors:  Deirdre Hahn; Elisabeth M Hodson; Lorraine A Hamiwka; Vincent Ws Lee; Jeremy R Chapman; Jonathan C Craig; Angela C Webster
Journal:  Cochrane Database Syst Rev       Date:  2019-12-16

2.  Efficacy and Safety of Tacrolimus-Based Maintenance Regimens in De Novo Kidney Transplant Recipients: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.

Authors:  Manjunatha T A; Rebecca Chng; Wai-Ping Yau
Journal:  Ann Transplant       Date:  2021-12-29       Impact factor: 1.530

Review 3.  Mammalian Target of Rapamycin Inhibitors and Wound Healing Complications in Kidney Transplantation: Old Myths and New Realities.

Authors:  Muhammad Abdul Mabood Khalil; Saeed M G Al-Ghamdi; Ubaidullah Shaik Dawood; Said Sayed Ahmed Khamis; Hideki Ishida; Vui Heng Chong; Jackson Tan
Journal:  J Transplant       Date:  2022-02-28

Review 4.  Medical Aspects of mTOR Inhibition in Kidney Transplantation.

Authors:  Elena Cuadrado-Payán; Fritz Diekmann; David Cucchiari
Journal:  Int J Mol Sci       Date:  2022-07-12       Impact factor: 6.208

5.  Effect of Sirolimus vs. Everolimus on CMV-Infections after Kidney Transplantation-A Network Meta-Analysis.

Authors:  Sebastian Wolf; Verena S Hoffmann; Florian Sommer; Matthias Schrempf; Mingming Li; Martin Ryll; Ulrich Wirth; Matthias Ilmer; Jens Werner; Joachim Andrassy
Journal:  J Clin Med       Date:  2022-07-20       Impact factor: 4.964

  5 in total

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