University of Miami.
Crit Rev Oncog. 2024;29(3):83-90. doi: 10.1615/CritRevOncog.2024051588.
The current rapid development of more selective and effective drugs for the treatment of thyroid cancer has open a new era in the treatment of patients with this condition, in the past limited to the possibility of only radioactive iodine for well differentiated tumor and surgery for medullary thyroid carcinoma (MTC). The treatment of advanced medullary thyroid carcinoma has evolved in the last few years and options for patients with advanced disease are now available. Multikinase inhibitors (MKIs) with nonselective RET inhibition like Vandetanib and Cabozantinib were approved for the treatment of MTC, although the efficacy is limited due to the lack of specificity resulting in a higher rate of drug-related adverse events, leading to subsequent dose reductions, or discontinuation, and the development of a resistance mechanism like seen on the RET Val804 gatekeeper mutations. MTC is associated with mutations in the RET protooncogene, and new highly selective RET inhibitors have been developed including Selpercatinib and Pralsetinib, drugs that have demonstrate excellent results in clinical trials, and efficacy even in the presence of gatekeeper mutations. However, despite their efficacy and great tolerability, mechanisms of resistance have been described, such as the RET solvent front mutations. Due to this, the need of constant evolution and drug research is necessary to overcome the emergence of resistance mechanisms.
当前,治疗甲状腺癌的选择性更强、效果更显著的药物快速发展,为这种疾病的治疗开启了一个新时代。过去,分化型肿瘤仅能采用放射性碘治疗,甲状腺髓样癌(MTC)只能采用手术治疗。近年来,晚期甲状腺髓样癌的治疗方法已经取得了进展,目前为晚期疾病患者提供了更多的选择。尽管由于缺乏特异性导致药物相关不良反应发生率较高,从而导致随后降低剂量或停药,以及产生耐药机制,如 RET Val804 守门突变,但非选择性 RET 抑制的多激酶抑制剂(MKIs)如凡德他尼和卡博替尼已被批准用于治疗 MTC。MTC 与 RET 原癌基因突变有关,已经开发出了新型高度选择性的 RET 抑制剂,包括塞尔帕替尼和普拉替尼,这些药物在临床试验中显示出了优异的效果,甚至在存在守门突变的情况下也有效。然而,尽管这些药物具有疗效和良好的耐受性,但已经描述了耐药机制,如 RET 溶剂前沿突变。因此,为了克服耐药机制的出现,需要不断地进行药物研究和发展。