Abstract
The present study was designed to determine the pharmacokinetic profiles of a once-daily
formulation of tacrolimus (CAS 104987-11-3; TAC-once) in patients before and after
introduction of renal transplantation. Pharmacokinetic parameters for tacrolimus were
almost comparable among patients receiving TAC- once before, 2 weeks after and 3 weeks
after renal transplantation. Among various parameters, Ctrough correlated most closely with the area under the concentration-time curve during 24
h (AUC0–24) (R2 = 0.82, P < 0.001), while no consistent correlation was observed between AUC0–24 and concentrations at 2 h or 4 h, or the dose of TAC-once. The clinical outcomes
such as the incidence of acute rejection, renal tissue injury and cytomegalovirus
infection were evaluated during the first 3 weeks and 3 months after transplantation,
and the data were compared with the historical data obtained from patients who had
received the conventional twice-daily formulation of tacrolimus (TAC-twice). There
were no significant differences in the incidence of such clinical outcomes between
the two groups. These findings suggest that Ctrough is useful for therapeutic monitoring of tacrolimus in patients receiving TAC-once.
In addition, pharmacokinetics and clinical outcomes were comparable between TAC-once
and TAC-twice formulations.
Key words
Area under the concentration-time curve - CAS 104987-11-3 - Pharmacokinetics - Renal
transplantation - Tacrolimus, once-daily formulation - Trough concentration