Abstract

Tacrolimus (TAC) is a first-choice immunosuppressant for solid organ transplantation, characterized by high potential for drug-drug interactions, significant inter- and intra-patient variability, and narrow therapeutic index. Therapeutic drug monitoring (TDM) of TAC concentrations in whole blood (WB) is capable of reducing the incidence of adverse events. Since TAC acts within lymphocytes, its monitoring in peripheral blood mononuclear cells (PBMC) may represent a valid future alternative for TDM. Nevertheless, TAC intracellular concentrations and their variability are poorly described, particularly in the pediatric context. Therefore, our aim was describing TAC concentrations in WB and PBMC and their variability in a cohort of pediatric patients undergoing constant immunosuppressive maintenance therapy, after liver transplantation. TAC intra-PBMCs quantification was performed through a validated UHPLC–MS/MS assay over a period of 2–3 months. There were 27 patients included in this study. No significant TAC changes in intracellular concentrations were observed (p = 0.710), with a median percent change of −0.1% (IQR −22.4%–+46.9%) between timings: this intra-individual variability was similar to the one in WB, −2.9% (IQR −29.4–+42.1; p = 0.902). Among different patients, TAC weight-adjusted dose and age appeared to be significant predictors of TAC concentrations in WB and PBMC. Intra-individual seasonal variation of TAC concentrations in WB, but not in PBMC, have been observed. These data show that the intra-individual variability in TAC intracellular exposure is comparable to the one observed in WB. This opens the way for further studies aiming at the identification of therapeutic ranges for TAC intra-PBMC concentrations.

Highlights

  • Tacrolimus (TAC) is among the most used first-line immunosuppressant drug for the prevention of posttransplantation graft rejection (Staatz et al, 2004; Staatz and Tett, 2004)

  • The Therapeutic drug monitoring (TDM) of TAC concentrations in whole blood (WB) entered in the common clinical practice for the management of the immunosuppressive treatment after solid organ transplantation (Brunet et al, 2019)

  • This is due to the knowledge of therapeutic ranges associated with low probability of graft rejection and toxicity (Brunet et al, 2019; Lemaitre et al, 2020b)

Read more

Summary

Introduction

Tacrolimus (TAC) is among the most used first-line immunosuppressant drug for the prevention of posttransplantation graft rejection (Staatz et al, 2004; Staatz and Tett, 2004). Despite a rather good effectiveness and tolerability, this drug shows a narrow therapeutic range and quite high intraand inter-patient variability in its concentrations in whole blood (WB) (Bahmany et al, 2018; Kaneko et al, 2018; Álvarez et al, 2020). For these reasons, therapeutic drug monitoring (TDM) is indicated in order to guide therapeutic adjustments during treatment, in the early phase posttransplantation, and regularly during the maintenance phase. Intra-patient variability in drug concentrations represents an important challenge for TDM, since it causes the need for a closer monitoring: a too high intraindividual variability in the absence of significant clinical or therapeutic changes would limit the usefulness of TDM

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call