| Literature DB >> 27639190 |
F J Bemelman1, J W de Fijter2, J Kers3, C Meyer4, H Peters-Sengers1, E F de Maar5, K A M I van der Pant1, A P J de Vries2, J-S Sanders5, A Zwinderman6, M M Idu7, S Berger5, M E J Reinders2, C Krikke8, I M Bajema9, M C van Dijk10, I J M Ten Berge1, J Ringers11, J Lardy12, D Roelen13, D-J Moes14, S Florquin3, J J Homan van der Heide5.
Abstract
In renal transplantation, use of calcineurin inhibitors (CNIs) is associated with nephrotoxicity and immunosuppression with malignancies and infections. This trial aimed to minimize CNI exposure and total immunosuppression while maintaining efficacy. We performed a randomized controlled, open-label multicenter trial with early cyclosporine A (CsA) elimination. Patients started with basiliximab, prednisolone (P), mycophenolate sodium (MPS), and CsA. At 6 months, immunosuppression was tapered to P/CsA, P/MPS, or P/everolimus (EVL). Primary outcomes were renal fibrosis and inflammation. Secondary outcomes were estimated glomerular filtration rate (eGFR) and incidence of rejection at 24 months. The P/MPS arm was prematurely halted. The trial continued with P/CsA (N = 89) and P/EVL (N = 96). Interstitial fibrosis and inflammation were significantly decreased and the eGFR was significantly higher in the P/EVL arm. Cumulative rejection rates were 13% (P/EVL) and 19% (P/CsA), (p = 0.08). A post hoc analysis of HLA and donor-specific antibodies at 1 year after transplantation revealed no differences. An individualized immunosuppressive strategy of early CNI elimination to dual therapy with everolimus was associated with decreased allograft fibrosis, preserved allograft function, and good efficacy, but also with more serious adverse events and discontinuation. This can be a valuable alternative regimen in patients suffering from CNI toxicity. © Copyright 2016 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: calcineurin inhibitor (CNI); clinical research/practice; clinical trial; immunosuppressant; immunosuppression/immune modulation; kidney transplantation/nephrology
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Year: 2016 PMID: 27639190 DOI: 10.1111/ajt.14048
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086