Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective

卡波扎尼布 伦瓦提尼 医学 索拉非尼 背景(考古学) 肿瘤科 内科学 甲状腺癌 甲状腺癌 阿西替尼 全身疗法 靶向治疗 耐火材料(行星科学) 癌症 癌症研究 甲状腺 乳腺癌 肝细胞癌 古生物学 物理 天体生物学 生物
作者
Alice Nervo,Francesca Retta,Alberto Ragni,Alessandro Piovesan,Marco Gallo,Emanuela Arvat
出处
期刊:Cancer management and research [Dove Medical Press]
卷期号:Volume 14: 3047-3062 被引量:17
标识
DOI:10.2147/cmar.s340967
摘要

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.
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