Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jun;91(6):1600-1606.
doi: 10.1111/bcp.16098. Epub 2024 Jun 6.

Therapeutic drug monitoring of tacrolimus after kidney transplantation: trough concentration or area under curve-based monitoring?

Affiliations
Review

Therapeutic drug monitoring of tacrolimus after kidney transplantation: trough concentration or area under curve-based monitoring?

Teun van Gelder et al. Br J Clin Pharmacol. 2025 Jun.

Abstract

Measurement of pre-dose tacrolimus concentrations, also referred to as trough concentrations or C0 (in this paper the term C0 will be used), is the most frequently used parameter for therapeutic drug monitoring in patients after solid organ transplantation. C0 is relatively easy to obtain, and can be combined with other lab tests. C0 monitoring is convenient for patient and hospital staff. Adjusting the dose based on C0 assumes that the C0 has a good correlation with the overall exposure to the drug, as reflected in the area under concentration-time curve (AUC). However, C0 may not be the panacea it is suggested to be, and there are patients who may benefit from additional measurements to more precisely assess drug exposure. Especially in patients with a low C0/dose ratio, the peak tacrolimus concentrations after oral administration may be unexpectedly high, resulting in toxicity and (as has been shown already) in poor long-term graft survival. At the other extreme, patients who only need a very low dose to reach target C0 may have a low peak and also a low AUC and may be underexposed. In this paper, the limitations of C0 will be discussed, and the type of studies needed to provide the evidence for implementation of more sophisticated therapeutic drug monitoring. The paper focuses on treatment of adult kidney transplant recipients.

Keywords: kidney; pharmacokinetics; tacrolimus; therapeutic drug monitoring; transplantation.

PubMed Disclaimer

Conflict of interest statement

In the last 3 years T.v.G. has received lecture fees and consulting fees from Roche Diagnostics, Thermo Fisher, Vitaeris, Otsuka, CSL Behring, Astellas and Aurinia Pharma. In all cases money has been transferred to hospital accounts, and none has been paid to his personal bank accounts. T.v.G. does not have employment or stock ownership at any of these companies, and neither does he have patents or patent applications.

References

    1. Brunet M, van Gelder T, Åsberg A, et al. Therapeutic drug monitoring of tacrolimus‐personalized therapy: second consensus report. Ther Drug Monit. 2019;41(3):261‐307. doi: 10.1097/FTD.0000000000000640 - DOI - PubMed
    1. Bergan S, Brunet M, Hesselink DA, et al. Personalized therapy for mycophenolate: consensus report by the International Association of Therapeutic Drug Monitoring and Clinical Toxicology. Ther Drug Monit. 2021;43(2):150‐200. doi: 10.1097/FTD.0000000000000871 - DOI - PubMed
    1. Rousseau A, Laroche ML, Venisse N, et al. Cost‐effectiveness analysis of individualized mycophenolate mofetil dosing in kidney transplant patients in the APOMYGRE trial. Transplantation. 2010;89(10):1255‐1262. doi: 10.1097/TP.0b013e3181d75952 - DOI - PubMed
    1. KDIGO clinical practice guideline for the care of kidney transplant recipients. Kidney disease: improving global outcomes (KDIGO) transplant work group. Am J Transplant. 2009;9(Suppl 3):S1‐S155. doi: 10.1111/j.1600-6143.2009.02834.x - DOI - PubMed
    1. Lemaitre F, Hesselink DA. TDM is alive and kicking! Ther Drug Monit. 2023;45(1):3‐5. doi: 10.1097/FTD.0000000000001034 - DOI - PubMed

MeSH terms