Enokida Tomohiro, Tahara Makoto
Department of Head and Neck Medical Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa 277-8577, Japan.
Cancers (Basel). 2021 Nov 4;13(21):5536. doi: 10.3390/cancers13215536.
Recent advances in the development of multitarget tyrosine kinase inhibitors (MTKIs), which mainly target the vascular endothelial growth factor receptor (VEGFR), have improved prognoses and dramatically changed the treatment strategy for advanced thyroid cancer. However, adverse events related to this inhibition can interrupt treatment and sometimes lead to discontinuation. In addition, they can be annoying and potentially jeopardize the subjects' quality of life, even allowing that the clinical outcome of patients with advanced thyroid cancer remains limited. In this review, we summarize the potential mechanisms underlying these adverse events (hypertension, proteinuria and renal impairment, hemorrhage, fistula formation/gastrointestinal perforation, wound healing, cardiovascular toxicities, hematological toxicity, diarrhea, fatigue, and acute cholecystitis), their characteristics, and actual management. Furthermore, we also discuss the importance of related factors, including alternative treatments that target other pathways, the necessity of subject selection for safer administration, and patient education.
多靶点酪氨酸激酶抑制剂(MTKIs)主要靶向血管内皮生长因子受体(VEGFR),其研发方面的最新进展改善了晚期甲状腺癌的预后,并显著改变了治疗策略。然而,这种抑制相关的不良事件可能会中断治疗,有时甚至导致停药。此外,这些不良事件可能令人烦恼,并可能危及受试者的生活质量,即使晚期甲状腺癌患者的临床结局仍然有限。在本综述中,我们总结了这些不良事件(高血压、蛋白尿和肾功能损害、出血、瘘管形成/胃肠道穿孔、伤口愈合、心血管毒性、血液学毒性、腹泻、疲劳和急性胆囊炎)潜在的机制、其特征及实际管理。此外,我们还讨论了相关因素的重要性,包括靶向其他途径的替代治疗、为更安全给药进行受试者选择的必要性以及患者教育。