Exelixis, Inc, Alameda, CA, USA.
Ann Arbor Pharmacometrics Group, Inc, Ann Arbor, MI, USA.
J Clin Pharmacol. 2019 Nov;59(11):1551-1561. doi: 10.1002/jcph.1467. Epub 2019 Jun 11.
An integrated population pharmacokinetic (PPK) model was used to evaluate the effects of liver dysfunction on the pharmacokinetics (PK) of cabozantinib in patients with hepatocellular carcinoma and to determine whether clinical dosage adjustment may be necessary in this population. An integrated PPK model previously developed in healthy volunteers and patients with various cancer types was updated with cabozantinib concentration data from hepatocellular carcinoma patients in phase 2 and 3 studies (total 2023; hepatocellular carcinoma 489 patients). Covariate effects of cancer type including hepatocellular carcinoma population and liver dysfunction per the National Cancer Institute Organ Dysfunction Working Group criteria were evaluated (normal 1425; mild liver dysfunction 558; moderate/severe liver dysfunction 15/1 patients). With hepatocellular carcinoma patients, PK parameter estimates and covariate effects were similar to the previous PPK model (2 compartments with first- and zero-order absorption and first-order elimination). Only medullary thyroid cancer had appreciable PK differences from healthy volunteers. PK parameter estimates were similar with and without addition of liver dysfunction covariates. Patients with mild liver dysfunction were predicted to have minimal differences in apparent clearance of cabozantinib relative to patients with normal liver function. Therefore, no initial cabozantinib dosage adjustment is recommended for cancer patients with mild liver dysfunction. The small sample size for patients with moderate and severe liver dysfunction limited dosing recommendations in these subpopulations. The results from this PPK analysis were different from those of the single-dose hepatic impairment study in healthy volunteers and more reflective of exposure in cancer patients following daily cabozantinib dosing.
采用群体药代动力学(PPK)模型评估肝功能障碍对肝细胞癌患者卡博替尼药代动力学(PK)的影响,并确定在此人群中是否需要临床剂量调整。先前在健康志愿者和各种癌症类型患者中开发的整合 PPK 模型,根据 2 期和 3 期研究(共 2023 例;肝细胞癌患者 489 例)中肝细胞癌患者的卡博替尼浓度数据进行了更新。评估了包括肝细胞癌人群和根据国家癌症研究所器官功能障碍工作组标准的肝功能障碍在内的癌症类型的协变量效应(正常 1425 例;轻度肝功能障碍 558 例;中度/重度肝功能障碍 15/1 例)。对于肝细胞癌患者,PK 参数估计值和协变量效应与之前的 PPK 模型相似(2 个隔室,具有 1 阶和零阶吸收和 1 阶消除)。只有甲状腺髓样癌与健康志愿者相比具有明显的 PK 差异。有无肝功能障碍协变量的加入,PK 参数估计值相似。轻度肝功能障碍患者预计与肝功能正常患者相比,卡博替尼的表观清除率差异最小。因此,不建议轻度肝功能障碍的癌症患者初始调整卡博替尼剂量。中重度肝功能障碍患者的样本量小,限制了这些亚人群的剂量建议。与健康志愿者单次剂量肝损伤研究的结果不同,该 PPK 分析更能反映癌症患者每日接受卡博替尼治疗后的暴露情况。