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Abstract

HERAKLES was a 1-year randomized, multicenter trial. Patients were randomized at 3 months after kidney transplantation to remain on cyclosporine-based therapy, switch to everolimus without a calcineurin inhibitor (CNI), or switch to everolimus with low-exposure cyclosporine. Overall, 417 of 497 (83.9%) patients from the core study entered a 4-year extension study. The randomized regimen was continued to year 5 in 75.9%, 41.9% and 24.6% of patients in the standard-CNI, CNI-free and low-CNI groups, respectively. Adjusted estimated GFR at year 5 was significantly higher in the CNI-free group versus standard CNI (difference 7.2 mL/min/1.73 m2, P <.001) or low CNI (difference 7.6 mL/min/1.73 m2, P <.001). For patients who continued randomized therapy for 5 years, differences were 14.4 mL/min/1.73 m2 and 10.1 mL/min/1.73 m2, respectively. Biopsy-proven acute rejection occurred during the 4-year extension study in 7.6%, 8.6%, and 9.0% of patients in the standard-CNI, CNI-free and low-CNI groups, respectively (P =.927). In conclusion, conversion to a CNI-free everolimus regimen 3 months after kidney transplantation improved long-term graft function, particularly in patients who continued the CNI-free regimen. Low CNI with everolimus did not improve renal function. Efficacy was comparable between groups but frequent immunosuppression changes should be taken into account.

OriginalspracheEnglisch
ZeitschriftAmerican Journal of Transplantation
Jahrgang18
Ausgabenummer12
Seiten (von - bis)2965-2976
Seitenumfang12
ISSN1600-6135
DOIs
PublikationsstatusVeröffentlicht - 12.2018

Fördermittel

The study was funded by Novartis Pharma GmbH, Nuernberg, Germany. The company also provided funding for freelance medical writing support. The authors of this manuscript have conflicts of interest to disclose as described by the American Journal of Transplantation. Claudia Sommerer’s institution has received research funding from Chiesi and Novartis. Michael Duerr has received honoraria and/or research funds from Bristol-Myers Squibb, Shire, Alexion, and Novartis, and has received travel grants from Roche and Astellas. Oliver Witzke has received research funds and/or honoraria from Alexion, Astellas, Bristol-Myers Squibb, Chiesi, Janssen-Cilag, MSD, Novartis, Pfizer, Roche, and Shire. Wolfgang Arns has received research funds and/or honoraria from Astellas, Chiesi, and Novartis. Frank Lehner has received research funds and/or honoraria from Astellas, Bristol-Myers Squibb, Chiesi, Fresenius, Hexal, Novartis, Pfizer, and Roche Pharma. Markus Guba has membership on an advisory board (Novartis) and a travel grant from Astellas. Johannes Jacobi has no conflicts of interest to disclose. Volker Kliem has received honoraria and fees from Astellas, Chiesi, Novartis, and Roche Pharma. Daniel Ackermann has no conflicts of interest to disclose. Petra Reinke has received research funds, honoraria, advisory board from Teva, ThermoFisher, Pfizer, Astellas, Amgen, Baxalta; MSD and Pluriste. Ingeborg A. Hauser has received research funds, travel grants and/or honoraria from Alexion, Astellas, Chiesi, Hexal, Novartis, Roche, Sanofi, and Teva. Rolf Stahl has no conflicts of interest to disclose. Thomas Rath has no conflicts of interest to disclose. Justyna Veit is an employee of Novartis. Martina Porstner is an employee of Novartis. Arianeb Mehrabi has no conflicts of interest to disclose. Klemens Budde has received research funds and/or honoraria from Abbvie, Alexion, Astellas, Bristol-Myers Squibb, Chiesi, Fresenius, Genentech, Hexal, Novartis, Otsuka, Pfizer, Roche, Shire, Siemens, and Veloxis Pharma.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

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