Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/30219
Title: Reduced exposure to calcineurin inhibitors in renal transplantation
Authors: Ekberg, Henrik
Tedesco-Silva, Helio
Demirbas, Alper
Vitko, Stefan
Nashan, Bjorn
Guerkan, Alp
Margreiter, Raimund
Hugo, Christian
Grinyo, Josep M.
Frei, Ulrich
Vanrenterghem, Yves
Daloze, Pierre
Halloran, Philip F.
ELITE Symphony Study
Lund Univ
Universidade Federal de São Paulo (UNIFESP)
Akdeniz Univ
Inst Klin & Expt Med
Hannover Med Sch
SB Tepecik Hosp
Univ Klin
Univ Hosp
Ciutat Univ Bellvitge
Free Univ Berlin
Katholieke Univ Leuven
CHU Montpellier
Univ Alberta
Issue Date: 20-Dec-2007
Publisher: Massachusetts Medical Soc
Citation: New England Journal of Medicine. Waltham: Massachusetts Medical Soc, v. 357, n. 25, p. 2562-2575, 2007.
Abstract: Background: Immunosuppressive regimens with the fewest possible toxic effects are desirable for transplant recipients. This study evaluated the efficacy and relative toxic effects of four immunosuppressive regimens.Methods: We randomly assigned 1645 renal-transplant recipients to receive standard-dose cyclosporine, mycophenolate mofetil, and corticosteroids, or daclizumab induction, mycophenolate mofetil, and corticosteroids in combination with low-dose cyclosporine, low-dose tacrolimus, or low-dose sirolimus. the primary end point was the estimated glomerular filtration rate (GFR), as calculated by the Cockcroft-Gault formula, 12 months after transplantation. Secondary end points included acute rejection and allograft survival.Results: the mean calculated GFR was higher in patients receiving low-dose tacrolimus (65.4 ml per minute) than in the other three groups (range, 56.7 to 59.4 ml per minute). the rate of biopsy-proven acute rejection was lower in patients receiving low-dose tacrolimus (12.3%) than in those receiving standard-dose cyclosporine (25.8%), low-dose cyclosporine (24.0%), or low-dose sirolimus (37.2%). Allograft survival differed significantly among the four groups (P=0.02) and was highest in the low-dose tacrolimus group (94.2%), followed by the low-dose cyclosporine group (93.1%), the standard-dose cyclosporine group (89.3%), and the low-dose sirolimus group (89.3%). Serious adverse events were more common in the low-dose sirolimus group than in the other groups (53.2% vs. a range of 43.4 to 44.3%), although a similar proportion of patients in each group had at least one adverse event during treatment (86.3 to 90.5%).Conclusions: A regimen of daclizumab, mycophenolate mofetil, and corticosteroids in combination with low-dose tacrolimus may be advantageous for renal function, allograft survival, and acute rejection rates, as compared with regimens containing daclizumab induction plus either low-dose cyclosporine or low-dose sirolimus or with standard-dose cyclosporine without induction. (ClinicalTrials.gov number, NCT00231764.).
URI: http://repositorio.unifesp.br/handle/11600/30219
ISSN: 0028-4793
Other Identifiers: http://dx.doi.org/10.1056/NEJMoa067411
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.