Gastrointestinal Medical Oncology Clinic, University of California San Francisco, 1825 Fourth St, Fourth Floor, San Francisco, CA, 94158, USA.
Indiana University Health Simon Cancer Center, Indianapolis, IN, USA.
Target Oncol. 2020 Aug;15(4):549-565. doi: 10.1007/s11523-020-00736-8.
Cabozantinib is an oral multikinase inhibitor whose targets include vascular endothelial growth factor receptors, MET, and the TAM family of kinases (TYRO3, AXL, MER). Cabozantinib is approved for patients with advanced hepatocellular carcinoma who have been previously treated with sorafenib, based on improved overall survival and progression-free survival relative to placebo in the phase III CELESTIAL study. During CELESTIAL, the most common adverse events (AEs) experienced by patients receiving cabozantinib included palmar-plantar erythrodysesthesia, fatigue, gastrointestinal-related events, and hypertension. These AEs can significantly impact treatment tolerability and patient quality of life. However, AEs can be effectively managed with supportive care and dose modifications. During CELESTIAL, more than half of the patients receiving cabozantinib required a dose reduction, while the rate of treatment discontinuation due to AEs was low. Here, we review the safety profile of cabozantinib and provide guidance on the prevention and management of the more common AEs, based on current evidence from the literature as well as our clinical experience. We consider the specific challenges faced by clinicians in treating this patient population and discuss factors that may affect exposure and tolerability to cabozantinib.
卡博替尼是一种口服多激酶抑制剂,其靶点包括血管内皮生长因子受体、MET 和 TAM 家族激酶(TYRO3、AXL、MER)。卡博替尼基于 III 期 CELESTIAL 研究中与安慰剂相比总生存期和无进展生存期的改善,被批准用于接受过索拉非尼治疗的晚期肝细胞癌患者。在 CELESTIAL 研究中,接受卡博替尼治疗的患者最常见的不良反应(AE)包括掌跖红细胞感觉不良、疲劳、胃肠道相关事件和高血压。这些 AE 可显著影响治疗耐受性和患者生活质量。然而,通过支持性护理和剂量调整可以有效地管理 AE。在 CELESTIAL 研究中,超过一半接受卡博替尼治疗的患者需要减少剂量,而由于 AE 导致的治疗中断率较低。在这里,我们根据文献中的现有证据以及我们的临床经验,回顾了卡博替尼的安全性概况,并提供了预防和管理更常见 AE 的指导。我们考虑了临床医生在治疗这一患者群体时面临的具体挑战,并讨论了可能影响卡博替尼暴露和耐受性的因素。