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Everolimus in de novo kidney transplant recipients participating in the Eurotransplant senior program: Results of a prospective randomized multicenter study (SENATOR)


Autoři: Susanne Brakemeier aff001;  Wolfgang Arns aff002;  Frank Lehner aff003;  Oliver Witzke aff004;  Oliver Vonend aff006;  Claudia Sommerer aff007;  Anja Mühlfeld aff008;  Thomas Rath aff009;  Robert Schuhmann aff002;  Bianca Zukunft aff001;  Irena Kroeger aff010;  Martina Porstner aff010;  Klemens Budde aff001
Působiště autorů: Department of Nephrology and Medical Intensive Care, Charité Campus Mitte, Berlin, Germany aff001;  Department of Nephrology and Transplantation, Cologne Merheim Medical Center, Cologne, Germany aff002;  Department of General, Visceral and Transplantation Surgery, Hannover Medical School, Hannover, Germany aff003;  Department of Infectious Diseases, University Duisburg-Essen, Essen, Germany aff004;  Department of Nephrology, University Duisburg-Essen, Essen, Germany aff005;  Department of Nephrology, University Dusseldorf, Medical Faculty, Dusseldorf, Germany aff006;  Department of Nephrology, University of Heidelberg, Heidelberg, Germany aff007;  Division of Nephrology and Immunology, University Hospital RWTH Aachen, Aachen, Germany aff008;  Department of Medicine III, Westpfalz- Kaiserslautern, Germany aff009;  Medical Department, Novartis Pharma GmbH, Nürnberg, Germany aff010
Vyšlo v časopise: PLoS ONE 14(9)
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pone.0222730

Souhrn

Early conversion to everolimus was assessed in kidney transplant recipients participating in the Eurotransplant Senior Program (ESP), a population in whom data are lacking. The SENATOR multicenter study enrolled 207 kidney transplant recipients undergoing steroid withdrawal at week 2 post-transplant (ClinicalTrials.gov [NCT00956293]). At week 7, patients were randomized (1:2 ratio) to continue the previous calcineurin inhibitor (CNI)-based regimen with mycophenolic acid (MPA) and cyclosporine or switch to a CNI-free regimen with MPA, everolimus (5–10 ng/mL) and basiliximab at weeks 7 and 12, then followed for 18 weeks to month 6 post-transplant. The primary endpoint was estimated GFR (eGFR). At week 7, 77/207 (37.2%) patients were randomized (53 everolimus, 24 control). At month 6, eGFR was comparable: 36.5±10.8ml/min with everolimus versus 42.0±13.0ml/min in the control group (p = 0.784). Discontinuation due to adverse events occurred in 27.8% of everolimus-treated patients and 0.0% of control patients (p = 0005). Efficacy profiles showed no difference. In conclusion, eGFR, safety and efficacy outcomes at month 6 post-transplant showed no difference between groups. The everolimus group experienced a higher rate of discontinuation due to adverse events. However, the high rate of non-randomization is highly relevant, indicating this to be a somewhat unstable patient population regardless of treatment.

Klíčová slova:

Biology and life sciences – Biochemistry – Research and analysis methods – People and places – Population groupings – Anatomy – Medicine and health sciences – Endocrinology – Endocrine disorders – Metabolic disorders – Pharmacology – Research design – Drugs – Age groups – Clinical research design – Adverse events – Biomarkers – Surgical and invasive medical procedures – Geriatrics – Elderly – Renal system – Transplantation – Organ transplantation – Renal transplantation – Urinary system procedures – Creatinine – Immunosuppressives


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