Literature DB >> 21697773

Conversion of long-term kidney transplant recipients from calcineurin inhibitor therapy to everolimus: a randomized, multicenter, 24-month study.

Hallvard Holdaas1, Lionel Rostaing, Daniel Serón, Edward Cole, Jeremy Chapman, Bengt Fellstrøm, Erik H Strom, Alan Jardine, Karsten Midtvedt, Uwe Machein, Bettina Ulbricht, Alexander Karpov, Philip J O'Connell.   

Abstract

BACKGROUND: Benefits of conversion from calcineurin inhibitor (CNI) to mammalian target of rapamycin inhibitor-based immunosuppression in long-term kidney transplant patients remain uncertain.
METHODS: ASCERTAIN was a 24-month, open-label, multicenter study. Kidney transplant patients more than 6 months posttransplant receiving CNI (baseline glomerular filtration rate [GFR] 30-70 mL/min/1.73 m) were randomized to everolimus with CNI elimination (n=127) or CNI minimization (n=144), or continued CNI unchanged (controls, n=123) to assess the effect on measured GFR at month 24 after randomization.
RESULTS: Renal function was stable in all groups to month 24. Mean measured GFR at month 24, the primary endpoint, was 48.0±22.0 mL/min/1.73 m, 46.6±21.1 mL/min/1.73 m, and 46.0±20.4 mL/min/1.73 m in the CNI elimination, CNI minimization, and control groups, respectively. Differences between CNI elimination (1.12 mL/min/1.73 m, 95% confidence interval [CI] -3.51 to 5.76, P=0.63) and CNI minimization (0.59 mL/min/1.73 m, 95% CI -3.88 to 5.07, P=0.79) versus controls at month 24 were nonsignificant that is, the primary endpoint was not met. No efficacy endpoint differed significantly between groups. Post hoc analyses showed that patients with baseline creatinine clearance (CrCl) more than 50 mL/min had a significantly greater increase in measured GFR after CNI elimination versus controls (difference 11.4 mL/min/1.73 m, 95% CI 2.1 to 20.8 mL/min/1.73 m, P=0.017). Adverse events resulted in discontinuation in 36 (28.3%) CNI elimination patients, 24 (16.7%) CNI minimization patients, and 5 (4.1%) controls (P<0.001 vs. CNI elimination; P=0.020 vs. CNI minimization).
CONCLUSION: Conversion to everolimus with CNI elimination or minimization a mean of 5.6 years after kidney transplantation had no overall renal benefit and was associated with more frequent adverse events and discontinuations. Patients with CrCl more than 50 mL/min may benefit from a change in therapy more than 6 months after renal transplantation.

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Year:  2011        PMID: 21697773     DOI: 10.1097/TP.0b013e318224c12d

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  34 in total

Review 1.  Everolimus-based calcineurin-inhibitor sparing regimens for kidney transplant recipients: a systematic review and meta-analysis.

Authors:  Liya Su; Ngalei Tam; Ronghai Deng; Philip Chen; Haibo Li; Linwei Wu
Journal:  Int Urol Nephrol       Date:  2014-07-16       Impact factor: 2.370

2.  Transplantation: mTOR inhibition in kidney transplant recipients.

Authors:  Sarah E Yost; Rochelle Byrne; Bruce Kaplan
Journal:  Nat Rev Nephrol       Date:  2011-08-30       Impact factor: 28.314

Review 3.  Calcineurin inhibitor withdrawal or tapering for kidney transplant recipients.

Authors:  Krishna M Karpe; Girish S Talaulikar; Giles D Walters
Journal:  Cochrane Database Syst Rev       Date:  2017-07-21

4.  In human cell cultures, everolimus is inferior to tacrolimus in inhibiting cellular alloimmunity, but equally effective as regards humoral alloimmunity.

Authors:  Theodoros Eleftheriadis; Georgios Pissas; Maria Sounidaki; Georgia Antoniadi; Nikolaos Antoniadis; Vassilios Liakopoulos; Ioannis Stefanidis
Journal:  Int Urol Nephrol       Date:  2017-05-15       Impact factor: 2.370

Review 5.  Roles of mTOR complexes in the kidney: implications for renal disease and transplantation.

Authors:  Daniel Fantus; Natasha M Rogers; Florian Grahammer; Tobias B Huber; Angus W Thomson
Journal:  Nat Rev Nephrol       Date:  2016-08-01       Impact factor: 28.314

6.  Inhibitors of mTOR and risks of allograft failure and mortality in kidney transplantation.

Authors:  T Isakova; H Xie; S Messinger; F Cortazar; J J Scialla; G Guerra; G Contreras; D Roth; G W Burke; M Z Molnar; I Mucsi; M Wolf
Journal:  Am J Transplant       Date:  2012-10-01       Impact factor: 8.086

Review 7.  Everolimus in kidney transplant recipients at high cardiovascular risk: a narrative review.

Authors:  Ernesto Paoletti; Franco Citterio; Alberto Corsini; Luciano Potena; Paolo Rigotti; Silvio Sandrini; Elisabetta Bussalino; Giovanni Stallone
Journal:  J Nephrol       Date:  2019-04-27       Impact factor: 3.902

8.  Differential risks for adverse outcomes 3 years after kidney transplantation based on initial immunosuppression regimen: a national study.

Authors:  Vikas R Dharnidharka; Mark A Schnitzler; Jiajing Chen; Daniel C Brennan; David Axelrod; Dorry L Segev; Kenneth B Schechtman; Jie Zheng; Krista L Lentine
Journal:  Transpl Int       Date:  2016-09-28       Impact factor: 3.782

9.  Mammalian Target of Rapamycin Inhibitors and Clinical Outcomes in Adult Kidney Transplant Recipients.

Authors:  Sunil V Badve; Elaine M Pascoe; Michael Burke; Philip A Clayton; Scott B Campbell; Carmel M Hawley; Wai H Lim; Stephen P McDonald; Germaine Wong; David W Johnson
Journal:  Clin J Am Soc Nephrol       Date:  2016-07-21       Impact factor: 8.237

10.  Identification and characterization of kidney transplants with good glomerular filtration rate at 1 year but subsequent progressive loss of renal function.

Authors:  Walter D Park; Timothy S Larson; Matthew D Griffin; Mark D Stegall
Journal:  Transplantation       Date:  2012-11-15       Impact factor: 4.939

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