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Minimization of maintenance immunosuppression early after renal transplantation: an interim analysis.

作者信息

Bemelman Frederike J, de Maar Eltjo F, Press Rogier R, van Kan Henrikus J, ten Berge Ineke J, Homan van der Heide Jaap J, de Fijter Hans W

机构信息

Department of Internal Medicine, Division of Nephrology, Academic Medical Center, Renal Transplant Unit, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Transplantation. 2009 Aug 15;88(3):421-8. doi: 10.1097/TP.0b013e3181af1df6.


DOI:10.1097/TP.0b013e3181af1df6
PMID:19667948
Abstract

INTRODUCTION: Chronic allograft nephropathy is the main cause of long-term renal transplant failure. Chronic use of calcineurin inhibitors contributes to its pathogenesis. Here, we report on a multicenter randomized trial to study the effects of withdrawal of cyclosporine A (CsA) from a triple immunosuppressive regimen containing CsA, prednisolone (P), and mycophenolate sodium (MPS) early after transplantation. METHODS: Patients continued on P/CsA, P/MPS, or P and everolimus (EVL). Before withdrawal, a transplant biopsy was performed ensuring no subclinical rejection was present. Drug levels were closely monitored. The primary outcome was interstitial graft fibrosis and hyalinosis. Secondary outcome was among others graft rejection. RESULTS: According to trial regulations, an interim analysis was performed after enrollment of half of the intended number of patients (n=113). Mean follow-up was 14+/-5 months from transplantation and 8+/-5 months from conversion. After conversion, acute rejection percentages were 3% in the P/CsA group, 22% in the P/MPS group, and 0% in the P/EVL group (P<0.009). CONCLUSIONS: We conclude that switching immunosuppressive therapy from P/CsA/MPS to therapy with P/CsA or P/EVL at 6 months after renal transplantation is effective in preventing rejection. Double therapy with P/MPS after withdrawal of P/CsA resulted in an increase in severe acute rejection episodes. These results were the immediate reason to halt the P/MPS arm. Serum creatinine values at the latest follow-up (8+/-5 months after conversion and 14+/-5 months after transplantation) in the P/EVL group were lower than in the P/CsA group.

摘要

相似文献

[1]
Minimization of maintenance immunosuppression early after renal transplantation: an interim analysis.

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[2]
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引用本文的文献

[1]
Interventions for BK virus infection in kidney transplant recipients.

Cochrane Database Syst Rev. 2024-10-9

[2]
Conversion From Calcineurin Inhibitors to Mammalian Target of Rapamycin Inhibitors in Kidney Transplant Recipients: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Front Immunol. 2021

[3]
Biopsy-Controlled Non-Invasive Quantification of Collagen Type VI in Kidney Transplant Recipients: A Post-Hoc Analysis of the MECANO Trial.

J Clin Med. 2020-10-7

[4]
Calcineurin inhibitor withdrawal or tapering for kidney transplant recipients.

Cochrane Database Syst Rev. 2017-7-21

[5]
Efficacy and Safety of Everolimus for Maintenance Immunosuppression of Kidney Transplantation: A Meta-Analysis of Randomized Controlled Trials.

PLoS One. 2017-1-20

[6]
Exploring genetic and non-genetic risk factors for delayed graft function, acute and subclinical rejection in renal transplant recipients.

Br J Clin Pharmacol. 2016-7

[7]
Renal transplantation with expanded criteria donors: Which is the optimal immunosuppression?

World J Transplant. 2016-3-24

[8]
Design and rationale of the ATHENA study--A 12-month, multicentre, prospective study evaluating the outcomes of a de novo everolimus-based regimen in combination with reduced cyclosporine or tacrolimus versus a standard regimen in kidney transplant patients: study protocol for a randomised controlled trial.

Trials. 2016-2-17

[9]
Effect of CYP3A4*22, CYP3A5*3, and CYP3A Combined Genotypes on Cyclosporine, Everolimus, and Tacrolimus Pharmacokinetics in Renal Transplantation.

CPT Pharmacometrics Syst Pharmacol. 2014-2-12

[10]
Population pharmacokinetics and pharmacogenetics of everolimus in renal transplant patients.

Clin Pharmacokinet. 2012-7-1

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