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Medline ® Abstract for Reference 129

of '肝病患者的化疗肝毒性和剂量调整'

129
TI
Epirubicin in patients with liver dysfunction: development and evaluation of a novel dose modification scheme.
AU
Dobbs NA, Twelves CJ, Gregory W, Cruickshanka C, Richards MA, Rubens RD
SO
Eur J Cancer. 2003;39(5):580.
 
This study aimed to develop an epirubicin dose modification scheme in women with breast cancer and liver dysfunction. We first identified target areas under the concentration-time curve (AUCs) of 2400 and 1600 ng/ml.h from pharmacokinetic studies in 15 women with normal liver tests. In a second group of 16 women with abnormal liver biochemistry, the relationship between raised asparate aminotransferase (AST) and epirubicin clearance was: dose=AUC (97.5-34.2xlog AST). Adaptive dosing was evaluated prospectively in a third group of 41 women with serum AST>or =2xnormal+/-raised bilirubin. The median AUCs were 2444 and 1608 ng/ml.h, close to the high and low target AUCs, respectively. Variability in AUC was lower with adaptive dosing than in a fourth group given an unadjusted dose of epirubicin (coefficient of variation=25.8, 30.0 and 46.5%, respectively; P=0.06). Epirubicin dosing based on AST is safe and may reduce pharmacokinetic variability.
AD
Breast Oncology Unit, GKT School of Medicine, Guy's Hospital, London, UK.
PMID