Department of Otorhinolaryngology, Head and Neck Surgery and the Abramson Cancer Center, University of Pennsylvania, United States.
Mayo Clinic-Rochester, United States.
Cancer Treat Rev. 2018 May;66:64-73. doi: 10.1016/j.ctrv.2018.04.007. Epub 2018 Apr 22.
Progress in the treatment of advanced medullary thyroid cancer (MTC) has resulted from the approval of 2 drugs within the past 5 years, vandetanib and cabozantinib. These multikinase inhibitors (MKIs) possess overlapping specificities for multiple kinase targets implicated in the progression of MTC. Both drugs are associated with toxicities, including hypertension, hemorrhage/perforation, diarrhea and other gastrointestinal events, several dermatologic events, and hypothyroidism. In addition, vandetanib is uniquely associated with QTc prolongation through interaction with myocardial potassium channels, and cabozantinib is uniquely associated with hand-foot skin reaction. Treatment-related toxicities occur frequently and can be severe or life-threatening, and patients undergoing long-term treatment will likely experience adverse events (AEs). Here we offer specific practical recommendations for managing AEs commonly occurring with vandetanib and cabozantinib. The recommended approach relies on early recognition and palliation of symptoms, dose interruption, and dose reduction as necessary in order for the patient to maintain the highest tolerable dose for as long as possible and optimal quality of life. Treatment guidelines do not specify a recommended sequence for treating with vandetanib and cabozantinib; however, most patients will receive both drugs during their lifetime. The choice for first-line therapy is individualized after a risk-benefit assessment and depends on physician preference and patient-related factors, such as comorbid conditions. Because most generalist practices may not be familiar with the intricacies of agents such as vandetanib and cabozantinib, we commend that patients with advanced MTC be managed and treated by a thyroid cancer specialist with coordination of care within a multidisciplinary team.
在过去的 5 年中,有 2 种药物被批准用于治疗晚期甲状腺髓样癌 (MTC),从而取得了进展。这些多激酶抑制剂 (MKIs) 对多种激酶靶点具有重叠的特异性,这些靶点与 MTC 的进展有关。这两种药物都与毒性相关,包括高血压、出血/穿孔、腹泻和其他胃肠道事件、几种皮肤事件以及甲状腺功能减退症。此外,vandetanib 通过与心肌钾通道相互作用而独特地导致 QTc 延长,而 cabozantinib 则独特地导致手足皮肤反应。治疗相关的毒性经常发生,并且可能严重或危及生命,接受长期治疗的患者可能会经历不良反应 (AE)。在这里,我们提供了针对 vandetanib 和 cabozantinib 常见不良反应的具体实用建议。建议的方法依赖于早期识别和症状缓解、剂量中断以及必要时的剂量减少,以便患者尽可能长时间地维持最高耐受剂量和最佳生活质量。治疗指南并未指定治疗 vandetanib 和 cabozantinib 的推荐顺序;然而,大多数患者在其一生中都会接受这两种药物的治疗。一线治疗的选择是个体化的,需要在风险效益评估后进行,取决于医生的偏好和患者相关因素,如合并症。由于大多数普通实践可能不熟悉 vandetanib 和 cabozantinib 等药物的复杂性,我们建议由甲状腺癌专家管理和治疗晚期 MTC 患者,并在多学科团队中协调护理。