Universitätsklinikum Frankfurt, Medizinische Klinik 1, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Drugs. 2020 Aug;80(12):1203-1210. doi: 10.1007/s40265-020-01361-5.
Cabozantinib (Cabometyx) is a potent multikinase inhibitor targeting the vascular endothelial growth factor (VEGF) receptor 2, the mesenchymal-epithelial transition factor (MET) receptor, and the "anexelekto" (AXL) receptor tyrosine kinase. It is approved for the treatment of advanced hepatocellular carcinoma (HCC) after failure of sorafenib in Europe (since November 2018) and in the USA (since January 2019). The approval of cabozantinib was based on results of the randomized, placebo-controlled, phase 3 CELESTIAL trial in patients with unresectable HCC, who received one or two prior lines of treatment including sorafenib. At the second planned interim analysis, the trial was stopped, because the primary end point overall survival was clearly in favor for cabozantinib. Additionally, median progression-free survival was superior to placebo. The most common ≥ grade 3 relevant adverse events in patients with HCC treated with cabozantinib were palmar-plantar erythrodysesthesia, hypertension, fatigue, and diarrhea. In this review, current data on cabozantinib for the treatment of patients with advanced HCC, with a focus on the management of common adverse events and ongoing clinical trials, are discussed.
卡博替尼(Cabometyx)是一种强效的多激酶抑制剂,针对血管内皮生长因子(VEGF)受体 2、间质上皮转化因子(MET)受体和“anexelekto”(AXL)受体酪氨酸激酶。它在欧洲(自 2018 年 11 月起)和美国(自 2019 年 1 月起)被批准用于索拉非尼治疗失败后的晚期肝细胞癌(HCC)的治疗。卡博替尼的批准基于在不可切除 HCC 患者中进行的随机、安慰剂对照、III 期 CELESTIAL 试验的结果,这些患者接受了一种或两种包括索拉非尼在内的一线治疗。在第二次计划的中期分析中,该试验因主要终点总生存期明显有利于卡博替尼而停止。此外,中位无进展生存期优于安慰剂。接受卡博替尼治疗的 HCC 患者中最常见的≥3 级相关不良事件是掌跖红细胞感觉异常、高血压、疲劳和腹泻。在这篇综述中,讨论了卡博替尼治疗晚期 HCC 患者的最新数据,重点是常见不良事件的管理和正在进行的临床试验。