Real life experience of mycophenolate mofetil monotherapy in liver transplant patients

Clin Res Hepatol Gastroenterol. 2021 Jan;45(1):101451. doi: 10.1016/j.clinre.2020.04.017. Epub 2020 Jun 11.

Abstract

Background: Mycophenolate mofetil (MMF) monotherapy following liver transplantation (LT) remains controversial due to a risk of acute rejection. The aim of this study was to report the largest multicenter experience of the use a MMF monotherapy guided by therapeutic drug monitoring using pharmacoslope modeling and Bayesian estimations of the MPA inter-dose AUC (BEAUCMPA) before withdrawing calcineurin inhibitors (CNI) and to evaluate the benefit of MMF monotherapy.

Methods: MMF daily doses were adjusted to reach the BEAUCMPA target of 45μg.h/mL. Then CNI were withdrawn and patients were followed on liver test and clinical outcomes.

Main findings: From 2000-2014, in 2 transplantation centers, 94 liver transplant recipients received MMF monotherapy 6.5±4 years after LT. The mean BEAUCMPA was 45.5±16μg.h/mL. During follow-up, 4 patients experienced acute rejection (4%). During the first year, estimated glomerular filtration rate (eGFR) improved from 46.2±10.5 to 49.1±11.5mL/kg/min (P=0.025). Benefit persisted at year 5. In patients with metabolic syndrome, eGFR did not improve.

Conclusion: MMF monotherapy regimen appears usually safe and beneficial, with low risk of acute rejection and eGFR improvement. Therapeutic drug monitoring strategy seemed useful by identifying 14% of patients with low MMF exposure.

Keywords: Acute rejection; Chronic kidney dysfunction; Liver transplantation; Mycophenolate mofetil.

Publication types

  • Multicenter Study

MeSH terms

  • Bayes Theorem
  • Calcineurin Inhibitors
  • Graft Rejection / prevention & control
  • Humans
  • Immunosuppressive Agents
  • Liver Transplantation*
  • Mycophenolic Acid*

Substances

  • Calcineurin Inhibitors
  • Immunosuppressive Agents
  • Mycophenolic Acid