Skip to main content
Orthotopic Liver Transplantation Using Low-dose Tacrolimus and Sirolimus
Liver Transplantation (2001)
  • Vivian C. McAlister, Dalhousie University
  • Kevork M. Peltekian, Dalhousie University
  • Dickran A. Malatjalian, Dalhousie University
  • Shannon Colohan, Dalhousie University
  • Sara MacDonald, Dalhousie University
  • Hinrich Bitter-Suermann, Dalhousie University
  • Allan S. MacDonald, Dalhousie University

Although sirolimus (SRL) binds the immunophilin FK506-binding protein-12 (FKBP-12) with greater avidity than tacrolimus (TAC), animal studies have shown that SRL and TAC act synergistically to prevent rejection. Dose-related toxicity is more often the cause of TAC discontinuation than rejection. We hypothesized that SRL would allow for a substantial reduction in the concomitant dose of TAC after liver transplantation to levels less than the threshold for toxicity. A series of 56 liver transplant recipients were administered a combination of SRL and TAC (target trough levels, 7 and 5 ng/mL, respectively). Planned weaning of steroids commenced after 3 months. Pharmacokinetic (PK) studies were undertaken. Patient and graft survival were 52 patients (93%) and 51 grafts (91%), with a follow-up of 23 months (range, 6 to 35 months). One episode (1.8%) of hepatic artery thrombosis was seen. The rate of acute cellular rejection was 14%. No extra treatment was administered in 3 of 8 patients, and the other 5 episodes responded to a single course of steroids. Cytomegalovirus infection occurred in 4 patients (7%). Renal function, glucose control, and lipid metabolism are near normal in 47 patients (84%) without additional medication. Steroid elimination is completed in 51 patients (91%). Bioavailability of SRL and TAC varied between transplant recipients, but trough levels strongly correlated with the area under the curve (r(2) = 0.82 and r(2) = 0.84, respectively). Simultaneous administration did not affect the PK profile of the drugs at this dose. The ratio of trough level to daily dose correlated between SRL and TAC. The synergistic effect seen in animal models also occurs in clinical liver transplant recipients on SRL-TAC combination immunosuppression. A low-dose combination of SRL and TAC should be compared with conventional immunosuppression in a multicenter, randomized, controlled trial.

  • Cytomegalovirus Infections,
  • Dose-Response Relationship,
  • Drug Combinations,
  • Drug Synergism,
  • Graft Rejection,
  • Immunosuppressive Agents,
  • Liver Transplantation,
  • Sirolimus,
  • Tacrolimus
Publication Date
August, 2001
Publisher Statement
Dr. Vivian McAlister is currently a faculty member at The University of Western Ontario.
Citation Information
Vivian C. McAlister, Kevork M. Peltekian, Dickran A. Malatjalian, Shannon Colohan, et al.. "Orthotopic Liver Transplantation Using Low-dose Tacrolimus and Sirolimus" Liver Transplantation Vol. 7 Iss. 8 (2001)
Available at: