Nervo Alice, Retta Francesca, Ragni Alberto, Piovesan Alessandro, Gallo Marco, Arvat Emanuela
Oncological Endocrinology Unit, Department of Medical Sciences, Città Della Salute e Della Scienza Hospital, University of Turin, Turin, Italy.
Endocrinology and Metabolic Diseases Unit, AO SS. Antonio e Biagio e Cesare Arrigo Hospital, Alessandria, Italy.
Cancer Manag Res. 2022 Oct 21;14:3047-3062. doi: 10.2147/CMAR.S340967. eCollection 2022.
Patients with thyroid cancer (TC) usually have an excellent prognosis; however, 5-10% of them develop an advanced disease. The prognosis of this subgroup is still favourable if the lesions respond to radioactive iodine (RAI) treatment. Nearly two-thirds of advanced TC patients become RAI-refractory (RAI-R), and their management is challenging. A multidisciplinary approach in the context of a tumour board is essential to define a personalized strategy. Systemic therapy is not always the best option. In case of slow neoplastic growth and low tumour burden, active surveillance may represent a valuable choice. Local approaches might be considered if the disease progression is limited to a single or few lesions, also in combination and during systemic therapy. Antiresorptive treatment may be started in presence of bone metastases. In case of rapid and/or symptomatic progression involving multiple lesions and/or organs, systemic therapy has to be considered, in absence of contraindications. The multi-kinase inhibitors (MKIs) lenvatinib and sorafenib are currently available as first-line treatment for advanced progressive RAI-R TC. Among second-line options, cabozantinib has been recently approved in RAI-R TC who progressed during MKIs targeting the vascular endothelial growth factor receptor (VEGFR). In the last few years, next-generation sequencing (NGS) assays have been increasingly employed, permitting identification of the genetic alterations harboured by TC, with a significant impact on patients' management. Novel selective targeted therapies have been introduced for the treatment of RAI-R TC in selected cases: REarranged during Transfection (RET) inhibitors (selpercatinib and pralsetinib) and Tropomyosin Receptor Kinase (TRK) inhibitors (larotrectinib and entrectinib) have recently expanded the panorama of the therapeutic options. Moreover, immune checkpoint inhibitors (ICIs) have shown promising results, and they are still under investigation.
甲状腺癌(TC)患者通常预后良好;然而,其中5%-10%会发展为晚期疾病。如果病变对放射性碘(RAI)治疗有反应,该亚组患者的预后仍然良好。近三分之二的晚期TC患者对RAI难治(RAI-R),其治疗具有挑战性。在肿瘤委员会的背景下采用多学科方法对于确定个性化策略至关重要。全身治疗并不总是最佳选择。在肿瘤生长缓慢且肿瘤负荷较低的情况下,主动监测可能是一个有价值的选择。如果疾病进展仅限于单个或少数病变,也可在全身治疗期间联合考虑局部治疗方法。存在骨转移时可开始抗吸收治疗。在出现涉及多个病变和/或器官的快速和/或有症状进展且无禁忌证的情况下,必须考虑全身治疗。多激酶抑制剂(MKIs)仑伐替尼和索拉非尼目前可作为晚期进展性RAI-R TC的一线治疗药物。在二线治疗选择中,卡博替尼最近已被批准用于在靶向血管内皮生长因子受体(VEGFR)的MKIs治疗期间进展的RAI-R TC患者。在过去几年中,下一代测序(NGS)检测方法的应用越来越广泛,有助于识别TC所携带的基因改变,对患者的治疗管理产生了重大影响。在某些特定情况下,已引入新型选择性靶向治疗药物用于治疗RAI-R TC:转染重排(RET)抑制剂(塞尔帕替尼和普拉替尼)和原肌球蛋白受体激酶(TRK)抑制剂(拉罗替尼和恩曲替尼)最近拓宽了治疗选择范围。此外,免疫检查点抑制剂(ICIs)已显示出有前景的结果,仍在研究中。