Three‐Year Efficacy and Safety Results from a Study of Everolimus Versus Mycophenolate Mofetil in de novo Renal Transplant Patients
| Autor: | Raimund Margreiter, Michael Winkler, Jacques Dantal, Klemens Budde, Willem Weimar, Hendrik G. Viljoen, Dirk Kuypers, Pavel Filiptsev, Stefan Vitko, Nathalie Cretin, Sami A. Sadek, Yulan Li, Ole Øyen |
|---|---|
| Přispěvatelé: | Internal Medicine |
| Rok vydání: | 2005 |
| Předmět: |
Adult
Graft Rejection Male medicine.medical_specialty Time Factors Adolescent Biopsy Urology Peripheral edema Kidney Mycophenolic acid Cohort Studies Double-Blind Method Adrenal Cortex Hormones medicine Humans Immunology and Allergy Pharmacology (medical) Everolimus Kidney transplantation Aged Antibacterial agent Sirolimus Transplantation business.industry Middle Aged Mycophenolic Acid medicine.disease Kidney Transplantation Surgery Treatment Outcome Tolerability Creatinine Cyclosporine Emulsions Female medicine.symptom business Immunosuppressive Agents medicine.drug |
| Zdroj: | American Journal of Transplantation, 5(10), 2521-2530. Wiley-Blackwell Publishing Ltd |
| ISSN: | 1600-6135 |
| DOI: | 10.1111/j.1600-6143.2005.01063.x |
| Popis: | Everolimus 1.5 or 3 mg/day was compared with mycophenolate mofetil (MMF) 2 g/day in a randomized, multicenter 36-month trial in de novo renal allograft recipients (n = 588) receiving cyclosporine microemulsion (CsA) and corticosteroids. The study was double-blind until all patients had completed 12 months, then open-label. By 36 months, graft loss occurred in 7.2, 16.7 and 10.7% of patients in the everolimus 1.5, 3 mg/day, and MMF groups, respectively (p = 0.0048 for everolimus 1.5 mg/day vs. 3 mg/day); efficacy failure (biopsy-proven acute rejection (BPAR), graft loss, death or lost to follow-up) occurred in 33.0, 38.9 and 37.2% of patients (p = 0.455 overall), respectively. Mortality and incidence of BPAR were comparable in all groups. Creatinine values were higher in everolimus groups, requiring a protocol amendment that recommended lower CsA exposure. Diarrhea, lymphocele, peripheral edema and hyperlipidemia were more common among everolimus-treated patients, whereas viral infections, particularly cytomegalovirus infection, increased in the MMF group. Overall safety and tolerability were better with MMF and everolimus 1.5 mg/day than with everolimus 3 mg/day. In conclusion, at 36 months, an immunosuppressive regimen containing everolimus 1.5 mg/day had equivalent patient, and graft survival and rejection rates compared with MMF in de novo renal transplant recipients, whereas everolimus 3 mg/day had inferior graft survival. Renal dysfunction in everolimus cohorts necessitates close monitoring. |
| Databáze: | OpenAIRE |
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