Meltdose tacrolimus population pharmacokinetics and limited sampling strategy evaluation in elderly kidney transplant recipients

Kamp, J.; Zwart, T.C.; Meziyerh, S.; Boog, P.J.M. van der; Nijgh, E.E.; Duin, K. van; ... ; Moes, D.J.A.R. (2024)

Article / Letter to editor

Background: Meltdose tacrolimus (Envarsus (R)) has been marketed as a formulation achieving a more consistent tacrolimus exposure. Due to the narrow therapeutic window of tacrolimus, dose individualization is essential. Relaxation of the upper age limits for kidney transplantations has resulted in larger numbers of elderly patients receiving tacrolimus. However, due to the physiological changes caused by aging, the tacrolimus pharmacokinetics (PK) might be altered. The primary aim was to develop a population PK model in elderly kidney transplant recipients. Secondary aims were the development and evaluation of a limited sampling strategy (LSS) for AUC estimation. Methods: A total of 34 kidney transplant recipients aged >= 65 years, starting on meltdose tacrolimus directly after transplantation, were included. An eight-point whole blood AUC0-24h and an abbreviated dried blood spot (DBS) AUC0-24h were obtained. The PK data were analyzed using nonlinear mixed effect modeling methods. Results: The PK data were best described using a two-compartment model, including three transit compartments and a mixture model for oral absorption. The best three-sample LSS was T = 0, 2, 6 h. The best four-sample LSSs were T = 0, 2, 6, 8 h and T = 0, 1, 6, 8 h. Conclusions: The developed population PK model adequately described the tacrolimus PK data in a population of elderly kidney transplant recipients. In addition, the developed population PK model and LSS showed an adequate estimation of tacrolimus exposure, and may therefore be used to aid in tacrolimus dose individualization.

• population pharmacokinetics
• tacrolimus
• prolonged release
• kidney transplantation
• elderly

• All authors: Kamp, J.; Zwart, T.C.; Meziyerh, S.; Boog, P.J.M. van der; Nijgh, E.E.; Duin, K. van; Vries, A.P.J. de; Moes, D.J.A.R.
• Date: 2024-01-01
• Journal: Pharmaceutics
• Volume: 16
• Issue: 1
• DOI: doi:10.3390/pharmaceutics16010017