Smith Deborah A, Koch Kevin M, Arya Nikita, Bowen Carolyn J, Herendeen Jill M, Beelen Andrew
Clinical Pharmacology Modelling & Simulation, GlaxoSmithKline, Inc., Research Triangle Park, NC, USA.
Br J Clin Pharmacol. 2009 Apr;67(4):421-6. doi: 10.1111/j.1365-2125.2009.03370.x.
To characterize the impact of potent CYP3A4 inhibition and induction on lapatinib pharmacokinetics.
Two studies were conducted in healthy subjects. One study examined the effect of ketoconazole 200 mg b.i.d. for 7 days on a single 100-mg dose of lapatinib in 22 healthy subjects. The other study examined the effect of carbamazepine titrated up to 200 mg b.i.d. over 20 days on a single 250-mg dose of lapatinib in 24 healthy subjects.
Ketoconazole altered lapatinib AUC, C(max) and half-life, with geometric mean [95% confidence interval (CI)] increases of 3.57-fold (3.07, 4.15), 2.14-fold (1.74, 2.64) and 1.66-fold (1.50, 1.84), respectively, but had no effect on absorption rate. Carbamazepine altered lapatinib AUC, C(max) and absorption rate, with geometric mean (95% CI) decreases of 72% (68, 77), 59% (49, 66) and 28% (4, 46), respectively, but had no effect on half-life.
Systemic exposure to lapatinib was significantly altered by potent inhibition and induction of CYP3A4. Dose adjustments may be required when lapatinib is administered with orally administered drugs that potently alter the activity of this enzyme.
描述强效细胞色素P450 3A4(CYP3A4)抑制和诱导对拉帕替尼药代动力学的影响。
在健康受试者中进行了两项研究。一项研究考察了22名健康受试者连续7天每天两次服用200mg酮康唑对单次100mg拉帕替尼剂量的影响。另一项研究考察了24名健康受试者在20天内将卡马西平滴定至每天两次200mg对单次250mg拉帕替尼剂量的影响。
酮康唑改变了拉帕替尼的曲线下面积(AUC)、最大血药浓度(Cmax)和半衰期,几何均值[95%置信区间(CI)]分别增加了3.57倍(3.07,4.15)、2.14倍(1.74,2.64)和1.66倍(1.50,1.84),但对吸收速率没有影响。卡马西平改变了拉帕替尼的AUC、Cmax和吸收速率,几何均值(95%CI)分别降低了72%(68,77)、59%(49,66)和28%(4,46),但对半衰期没有影响。
强效抑制和诱导CYP3A4可显著改变拉帕替尼的全身暴露量。当拉帕替尼与能有效改变该酶活性的口服药物联用时,可能需要调整剂量。