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A novel three‐dose regimen of daclizumab in liver transplant recipients with hepatitis C: A pharmacokinetic and pharmacodynamic study
Author(s) -
Washburn W. Kenneth,
Teperman Lewis W.,
Heffron Thomas G.,
Douglas David D.,
Gay Steven,
Katz Eliezer,
Klintmalm Goran B.G.
Publication year - 2006
Publication title -
liver transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.814
H-Index - 150
eISSN - 1527-6473
pISSN - 1527-6465
DOI - 10.1002/lt.20631
Subject(s) - daclizumab , medicine , cmax , regimen , liver transplantation , gastroenterology , pharmacokinetics , pharmacodynamics , tacrolimus , transplantation , pharmacology
This study evaluated the pharmacokinetics and pharmacodynamics of a novel 3‐dose regimen of daclizumab in de novo hepatitis C liver transplant recipients. In 30 of 156 recipients receiving daclizumab, mycophenolate mofetil, tacrolimus, and no steroids (Arm 3 of Hep C 3 Liver Study), daclizumab (2, 2, and 1 mg/kg, respectively) was given on days 1, 3, and 8 posttransplant, respectively, with trough, peak (C max ), and CD25 saturation (CD sat ) measured sequentially. Mean daclizumab C max was 50.3 μg/mL on day 1, and mean trough levels were 21.8, 25.7, and 9.9 μg/mL on days 3, 8, and 30, respectively. A significant decline in CD sat (mean, 15.7% to 4.7%) was observed on day 1 and was sustained throughout the study (2.8% on day 30). Daclizumab concentration ≥5 μg/mL was the level where most of the effect on CD sat was noticed. Elevated baseline CD sat was observed in African Americans, patients weighing ≤75 kg, and patients <60 years of age. After 365 days, 2 patients had experienced 3 rejections, 10 patients had recurrent hepatitis C, 4 patients died, and 2 grafts were lost. In conclusion, this novel 3‐dose regimen is effective in rapidly achieving high therapeutic concentration of daclizumab and a significant decline in CD sat lasting over 30 days. Liver Transpl 12:585–591, 2006. © 2006 AASLD.