Therapeutic monitoring of mycophenolate in transplantation: is it justified?
- PMID: 19275552
- DOI: 10.2174/138920009787522205
Therapeutic monitoring of mycophenolate in transplantation: is it justified?
Abstract
Mycophenolate mofetil (MMF) is the preferred antimetabolite in solid organ transplantation. It is a prodrug that undergoes pre-systemic metabolism to mycophenolic acid (MPA), the active drug moiety. MMF is typically administered as a fixed dose without routine monitoring of MPA concentrations. However, a role for therapeutic drug monitoring (TDM) of MPA has been suggested based on the drug's narrow therapeutic window and considerable between-subject variability. Dose-normalized MPA area under the concentration-time curve (AUC) has been observed to vary >/=10-fold. Some of this variability may be accounted for by patient variability in renal and liver function, serum albumin and haemoglobin levels, body mass, concomitant medication exposure and genetic polymorphisms in enzymes responsible for drug metabolism and transport, but much is unexplained. Widespread adoption of MPA TDM has been limited by the impracticality of full 0 to 12 hour AUC measurement (AUC(0-12)), poor correlation between pre-dose MPA concentration and AUC(0-12), ongoing questions regarding the utility of free versus total MPA measurements and lack of evidence correlating MPA exposure with clinical outcomes. Two recent randomized studies evaluating the role of MPA TDM in renal transplant recipients have reported conflicting results. Promising areas of ongoing study include use of Bayesian forecasting to predict MPA dosage and measurement of inosine monophosphate dehydrogenase activity. This review provides an overview of the pharmacokinetics of MMF in solid organ transplantation, and discusses the benefits and limitations of MPA monitoring. Areas that require additional research are identified.
Similar articles
-
Mycophenolate, clinical pharmacokinetics, formulations, and methods for assessing drug exposure.Transplant Rev (Orlando). 2011 Apr;25(2):47-57. doi: 10.1016/j.trre.2010.06.001. Epub 2010 Dec 28. Transplant Rev (Orlando). 2011. PMID: 21190834
-
Mycophenolate mofetil for solid organ transplantation: does the evidence support the need for clinical pharmacokinetic monitoring?Ther Drug Monit. 2003 Apr;25(2):137-57. doi: 10.1097/00007691-200304000-00003. Ther Drug Monit. 2003. PMID: 12657908 Review.
-
Clinical pharmacokinetics and pharmacodynamics of mycophenolate in solid organ transplant recipients.Clin Pharmacokinet. 2007;46(1):13-58. doi: 10.2165/00003088-200746010-00002. Clin Pharmacokinet. 2007. PMID: 17201457 Review.
-
Pharmacology and toxicology of mycophenolate in organ transplant recipients: an update.Arch Toxicol. 2014 Jul;88(7):1351-89. doi: 10.1007/s00204-014-1247-1. Epub 2014 May 4. Arch Toxicol. 2014. PMID: 24792322 Review.
-
Limited sampling model for advanced mycophenolic acid therapeutic drug monitoring after liver transplantation.Ther Drug Monit. 2014 Apr;36(2):141-7. doi: 10.1097/FTD.0b013e3182a37a1e. Ther Drug Monit. 2014. PMID: 24081208
Cited by
-
The correlation between the expression of genes involved in drug metabolism and the blood level of tacrolimus in liver transplant receipts.Sci Rep. 2017 Jun 13;7(1):3429. doi: 10.1038/s41598-017-02698-w. Sci Rep. 2017. PMID: 28611384 Free PMC article.
-
The influence of UGT polymorphisms as biomarkers in solid organ transplantation.Clin Chim Acta. 2012 Sep 8;413(17-18):1318-25. doi: 10.1016/j.cca.2012.01.031. Epub 2012 Feb 1. Clin Chim Acta. 2012. PMID: 22327003 Free PMC article. Review.
-
Pharmacokinetics, Pharmacodynamics, and Pharmacogenomics of Immunosuppressants in Allogeneic Hematopoietic Cell Transplantation: Part II.Clin Pharmacokinet. 2016 May;55(5):551-93. doi: 10.1007/s40262-015-0340-9. Clin Pharmacokinet. 2016. PMID: 26620047 Free PMC article. Review.
-
BK Virus in Kidney Transplant Recipients: The Influence of Immunosuppression.J Transplant. 2011;2011:750836. doi: 10.1155/2011/750836. Epub 2011 Jun 2. J Transplant. 2011. PMID: 21766009 Free PMC article.
-
Steady-state mycophenolate mofetil pharmacokinetic parameters enable prediction of systemic lupus erythematosus clinical flares: an observational cohort study.Arthritis Res Ther. 2010;12(6):R217. doi: 10.1186/ar3202. Epub 2010 Dec 22. Arthritis Res Ther. 2010. PMID: 21176194 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical