Pharmacokinetics and pharmacodynamics of AZD6244 (ARRY-142886) in tumor-bearing nude mice

被引:43
作者
Denton, Cathrine L. [3 ]
Gustafson, Daniel L. [1 ,2 ]
机构
[1] Colorado State Univ, Vet Teaching Hosp, Dept Clin Sci, Ft Collins, CO 80523 USA
[2] Univ Colorado, Ctr Canc, Aurora, CO 80045 USA
[3] Colorado State Univ, Vet Teaching Hosp, Anim Canc Ctr, Ft Collins, CO 80523 USA
基金
美国国家卫生研究院;
关键词
AZD6244; MEK inhibitor; PK/PD relationship; Hysteresis; KINASE KINASE-1/2 INHIBITOR; ORAL MEK INHIBITOR; BRAF MUTATIONS; PHASE-I; MELANOMA; CANCER; NRAS; MECHANISM; CI-1040; POTENT;
D O I
10.1007/s00280-010-1323-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
AZD6244 (ARRY-142886) (AstraZeneca, Macclesfield, UK) is a novel small molecule MEK1/2 inhibitor that is currently being tested in Phase II trials. With the recent publication of human pharmacokinetic data from clinical studies, we now know the achievable levels and range of AZD6244 exposure in humans. This study aimed to describe the pharmacokinetic profile of AZD6244 in mice in order to design preclinical studies that recapitulate exposure levels in humans. Male athymic, nude mice received subcutaneous inoculation of A375 human melanoma cells. Once tumors reached 400-700 mm(3), mice were given a single dose of either 5 or 10 mg/kg AZD6244 via oral gavage. Additionally, a subset of mice was dosed once daily for 1 week (10 mg/kg). Mice were killed and plasma and tissues were collected at various time points after the last dose. Samples were analyzed by LC/MS/MS for AZD6244 concentration. Additionally, pharmacodynamic endpoints such as tumor proliferation and ERK phosphorylation were analyzed at various time points after the last dose. After either a single dose or at steady state, at clinically equivalent exposures, AZD6244 effectively inhibits ERK phosphorylation and suppresses proliferation. Furthermore, we describe a hysteretic relationship between the pharmacokinetics and the pharmacodynamics of AZD6244 and both target and pharmacologic responses. The information presented herein will drive the rational design of pre-clinical studies that are not only relevant to the clinical setting, but also pave the way to understand the biological response to AZD6244 treatment.
引用
收藏
页码:349 / 360
页数:12
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