Hospital Universitario 12 de Octubre, Madrid, Spain.
Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Cancer Treat Rev. 2020 Sep;89:102062. doi: 10.1016/j.ctrv.2020.102062. Epub 2020 Jun 24.
Cabozantinib is an oral tyrosine kinase inhibitor (TKI) approved for the treatment of patients with advanced renal cell carcinoma (RCC) at a dose of 60 mg/day. As with other TKIs, cabozantinib is associated with high interpatient variability in drug clearance and exposure that can significantly impact safety and tolerability across a patient population. To optimize cabozantinib exposure (maintaining efficacy and tolerability) for the individual, patients may require treatment interruption with dose reduction (40 mg/day and then 20 mg/day). In the pivotal Phase 3 METEOR trial, cabozantinib significantly improved overall survival, progression-free survival and the objective response rate compared with everolimus in patients with advanced RCC who had received previous treatment with a VEGFR TKI. Dose reductions were common for patients receiving cabozantinib (60%) but effective as only 9% discontinued treatment due to adverse events (AEs). In this review, we discuss pharmacometric analyses that evaluated the impact of cabozantinib dose on efficacy and safety outcomes during the METEOR study. Exposure-response models demonstrate that the risk of experiencing adverse events and dose reduction is increased in patients with low cabozantinib clearance versus typical clearance and decreased in patients with high clearance. Dose reduction of cabozantinib to manage AEs is predicted to have minimal impact on efficacy as AEs are more likely to occur in patients with low clearance and higher exposure to cabozantinib. These analyses further support a dose modification strategy to optimize cabozantinib exposure for individual patients.
卡博替尼是一种口服酪氨酸激酶抑制剂(TKI),批准剂量为 60mg/天,用于治疗晚期肾细胞癌(RCC)患者。与其他 TKI 一样,卡博替尼的药物清除率和暴露量在患者之间存在很大的个体差异,这可能会显著影响整个患者群体的安全性和耐受性。为了优化卡博替尼的暴露量(保持疗效和耐受性),患者可能需要中断治疗并减少剂量(40mg/天,然后 20mg/天)。在关键的 3 期 METEOR 试验中,与依维莫司相比,卡博替尼显著改善了晚期 RCC 患者的总生存期、无进展生存期和客观缓解率,这些患者先前接受过 VEGFR TKI 治疗。接受卡博替尼治疗的患者剂量减少很常见(60%),但由于不良反应(AE)而停药的患者有效(仅 9%)。在这篇综述中,我们讨论了药代动力学分析,这些分析评估了 METEOR 研究期间卡博替尼剂量对疗效和安全性结果的影响。暴露-反应模型表明,与典型清除率相比,清除率低的患者发生不良反应和剂量减少的风险增加,而清除率高的患者则降低。为了管理不良反应而减少卡博替尼的剂量预计对疗效的影响最小,因为不良反应更可能发生在清除率低和卡博替尼暴露量高的患者中。这些分析进一步支持了一种剂量调整策略,以优化个体患者的卡博替尼暴露量。