Tacrolimus pharmacokinetics in BMT patients

• Published in: Bone marrow transplantation (Basingstoke) Vol. 21; no. 1; pp. 23 - 28
• Main Authors: BOSWELL, G. W, BEKERSKY, I, FAY, J, WINGARD, J, ANTIN, J, WEISDORF, D, MAHER, R, FITZSIMMONS, W, NASH, R
• Format: Journal Article
• Language: English
• Published: Basingstoke Nature Publishing Group 1998
• Subjects: Administration, Oral; Adult; Biological and medical sciences; Bone Marrow Transplantation; Female; Humans; Immunomodulators; Immunosuppressive Agents - pharmacokinetics; Infusions, Intravenous; Male; Medical sciences; Middle Aged; Pharmacology. Drug treatments; Tacrolimus - administration & dosage; Tacrolimus - pharmacokinetics; Human; Immunopathology; Corticosteroid; Chemoprophylaxis; Homograft; Graft versus host reaction; Malignant hemopathy; Methylprednisolone; Glucocorticoid; Prevention; Tacrolimus; Bone marrow; Complication; Graft; Immunosuppressive agent; Methotrexate; Pharmacokinetics
• ISSN: 0268-3369; 1476-5365
• DOI: 10.1038/sj.bmt.1701054

The pharmacokinetics of tacrolimus following its administration as monotherapy or in combination with corticosteroids or methotrexate to 31 BMT patients are presented. All patients received i.v. tacrolimus initially and were subsequently switched to p.o. dosing. Patients received methotrexate by i.v. bolus on post-transplantation days 1, 3, 6 and 11. Patients were started on i.v. corticosteroids beginning on post-transplantation day 7. The noncompartmental pharmacokinetics of tacrolimus based on whole blood concentrations were determined following the i.v. and p.o. doses and were not different at steady-state compared to a single dose. The mean terminal elimination half-life of tacrolimus was 18.2 h following i.v. administration; the total body clearance was 71 ml/h/kg, the volume of distribution was 1.67 1/kg. Co-administration of methylprednisolone or methotrexate did not significantly alter tacrolimus pharmacokinetics. The p.o. bioavailability was 31-49%. Trough blood concentrations (Cmin) at 0 h (pre-dose) and 12 h (post-dose) correlated well to AUC(0-12)indicating that, as in solid organ transplantation, Cmin was a good index of drug exposure. Correlation at 0 h (r = 0.92) and at 12 h (r = 0.93) indicate that either time point can be used for therapeutic drug monitoring in patient management.