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Three-year results of renal function in liver transplant recipients on low-dose sirolimus and tacrolimus: a multicenter, randomized, controlled trial

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LIVER TRANSPLANTATION
卷 29, 期 2, 页码 184-195

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/LVT.0000000000000003

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The aim of this study was to compare the effects of low-dose sirolimus and low-dose extended-release tacrolimus with normal-dose extended-release tacrolimus on renal function and rejection, graft and patient survival rates at 36 months after transplantation. This was an open-label, multicenter randomized controlled trial. The study found that there was no significant difference in the incidence of chronic kidney disease at 36 months between the groups, but in the intention-to-treat population, the interventional group had higher estimated glomerular filtration rate at 6 months.
The aim of this study was to investigate whether the combination of low-dose sirolimus (SRL) and low-dose extended-release tacrolimus (TAC) compared to normal-dose extended-release TAC results in a difference in the renal function and comparable rates of rejection, graft and patient survival at 36 months after transplantation. This study was an open-label, multicenter randomized, controlled trial. Patients were randomized to once-daily normal-dose extended-release TAC (control group) or once-daily combination therapy of SRL and low-dose extended-release TAC (interventional group). The primary endpoint was the cumulative incidence of chronic kidney disease (CKD) defined as grade >= 3 (estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m(2)) at 36 months after transplantation. In total, 196 patients were included. CKD at 36 months was not different between the control and interventional group (50.8%, 95% CI: 39.7%-59.9%) vs. 43.7%, 95% CI: 32.8%-52.8%). Only at 6 months after transplantation, the eGFR was higher in the interventional group compared to the control group (mean eGFR 73.1 +/- 15 vs. 67.6 +/- 16 mL/min/1.73 m(2), p=0.02) in the intention-to-treat population. No differences in the secondary endpoints and the number of serious adverse events were found between the groups. Once daily low-dose SRL combined with low-dose extended-release TAC does ultimately not provide less CKD grade >= 3 at 36 months compared to normal-dose extended-release TAC.

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