Ranson M, Wilson R H, O'Sullivan J M, Maruoka M, Yamaguchi A, Cowan R A, Logue J P, Tomkinson H, Tominaga N, Swaisland H, Oliver S, Usami M
Department of Medical Oncology, University of Manchester, Christie Hospital NHS Trust, Manchester, UK.
Int J Clin Pharmacol Ther. 2010 Nov;48(11):708-17. doi: 10.5414/cpp48708.
To investigate potential differences in zibotentan pharmacokinetics between Japanese and Caucasian patients with hormone-resistant prostate cancer (HRPC) following single and multiple dosing.
In the Japanese study, 18 patients received a single dose of zibotentan 5, 10 or 15 mg followed by 72 h washout before 26 days' once-daily dosing. In the Caucasian study, 21 patients received a single dose of zibotentan 5, 10 or 15 mg followed by 72 h washout before 12 days' once-daily dosing.
Pharmacokinetic parameters were similar between populations. Absorption of zibotentan was rapid with maximum plasma concentrations typically achieved within 3 h of dosing. Mean clearance, 17.9 and 18.7 ml/min in Japanese and Caucasian patients, respectively (range 7.0 - 36.3 ml/min in Japanese patients and 7.8 - 29.5 ml/min in Caucasian patients) and volume of distribution, 14.0 and 15.6 l for Japanese and Caucasian patients, respectively (range 7.9 - 29.1 l in Japanese patients and 9.6 - 23.8 l in Caucasian patients) were relatively low, and t1/2 was approximately 12 h (range 5.7 - 18.8 h in Japanese patients and 5.0 - 22.9 h in Caucasian patients) following single dosing. Little accumulation was observed following daily dosing and multiple-dose pharmacokinetics were predictable. Exposure levels achieved in some Japanese patients receiving zibotentan 15 mg were higher than those observed in Caucasian patients, however, this may be due to differences in body weight, as exposure levels were similar when data were normalized for body weight. Zibotentan was well tolerated in both populations.
There are no clinically relevant differences in the disposition and pharmacokinetics of zibotentan between Japanese and Caucasian patients with HRPC.
研究日本和高加索地区激素抵抗性前列腺癌(HRPC)患者在单剂量和多剂量给药后齐考诺肽药代动力学的潜在差异。
在日本的研究中,18名患者接受了5、10或15毫克单剂量的齐考诺肽,随后经过72小时的洗脱期,然后进行为期26天的每日一次给药。在高加索地区的研究中,21名患者接受了5、10或15毫克单剂量的齐考诺肽,随后经过72小时的洗脱期,然后进行为期12天的每日一次给药。
不同人群的药代动力学参数相似。齐考诺肽吸收迅速,给药后3小时内通常达到血浆最大浓度。日本和高加索地区患者的平均清除率分别为17.9和18.7毫升/分钟(日本患者范围为7.0 - 36.3毫升/分钟,高加索地区患者范围为7.8 - 29.5毫升/分钟),分布容积分别为14.0和15.6升(日本患者范围为7.9 - 29.1升,高加索地区患者范围为9.6 - 23.8升),相对较低,单剂量给药后t1/2约为12小时(日本患者范围为5.7 - 18.8小时,高加索地区患者范围为5.0 - 22.9小时)。每日给药后观察到很少有蓄积现象,多剂量药代动力学是可预测的。一些接受15毫克齐考诺肽的日本患者达到的暴露水平高于高加索地区患者,但这可能是由于体重差异,因为按体重对数据进行标准化后暴露水平相似。两个群体对齐考诺肽的耐受性都良好。
日本和高加索地区HRPC患者在齐考诺肽的处置和药代动力学方面没有临床相关差异。