| Literature DB >> 26285161 |
Philippe Gatault1,2, Dominique Bertrand3, Matthias Büchler1,2, Charlotte Colosio4, Bruno Hurault de Ligny5, Pierre-François Weestel6, Jean-Philippe Rerolle7, Antoine Thierry8, Johnny Sayegh9, Bruno Moulin10, Renaud Snanoudj11, Joseph Rivalan12, Anne-Elisabeth Heng13, Bénédicte Sautenet1, Yvon Lebranchu1,2.
Abstract
We present the results at 8 years of the Spiesser study, a randomized trial comparing de novo sirolimus and cyclosporine in kidney transplant recipients at low immunologic risk. We assessed estimated glomerular filtration (eGFR), graft, patient, and death-censored graft survival (log-rank compared), de novo DSA appearance, risk of malignancy, post-transplant diabetes mellitus (PTDM), and anemia. Intent-to-treat and on-treatment analyses were performed. Graft survival was similar in both groups (sirolimus: 73.3%, cyclosporine: 77.7, P = 0.574). No difference was observed between treatment groups concerning patient survival (P = 0.508) and death-censored graft survival (P = 0.858). In conditional intent-to-treat analysis, mean eGFR was greater in sirolimus than in cyclosporine group (62.5 ± 27.3 ml/min vs. 47.8 ± 17.1 ml/min, P = 0.004), in particular because graft function was excellent in patients maintained under sirolimus (eGFR = 74.0 ml/min). Importantly, no detrimental impact was observed in patients in whom sirolimus has been withdrawn (eGFR = 49.5 ml/min). Overall, 17 patients showed de novo DSAs, with no difference between the two groups (P = 0.520). Malignancy did not differ by treatment. An initial maintenance regimen based on sirolimus provides a long-term improvement in renal function for kidney transplant patients, especially for those maintained on sirolimus.Entities:
Keywords: clinical trial; human leukocyte antigen-antibody posttransplantation; immunosuppression; kidney transplantation; target of rapamycin-inhibitors
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Year: 2016 PMID: 26285161 DOI: 10.1111/tri.12656
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782