Department of Nuclear Medicine, The Third Affiliated Hospital of Kunming Medical University, Tumor Hospital of Yunnan Province, 519 Kunzhou Road, Xishan District, Kunming, KM, 650118, China.
Med Oncol. 2023 Jul 31;40(9):258. doi: 10.1007/s12032-023-02098-3.
Most patients with differentiated thyroid cancer have a good prognosis after radioactive iodine-131 treatment, but there are still a small number of patients who are not sensitive to radioiodine treatment and may subsequently show disease progression. Therefore, radioactive-iodine refractory differentiated thyroid cancer treated with radioiodine usually shows reduced radioiodine uptake. Thus, when sodium iodine symporter expression, basolateral membrane localization and recycling degradation are abnormal, radioactive-iodine refractory differentiated thyroid cancer may occur. In recent years, with the deepening of research into the pathogenesis of this disease, an increasing number of molecules have become or are expected to become therapeutic targets. The application of corresponding inhibitors or combined treatment regimens for different molecular targets may be effective for patients with advanced radioactive-iodine refractory differentiated thyroid cancer. Currently, some targeted drugs that can improve the progression-free survival of patients with radioactive-iodine refractory differentiated thyroid cancer, such as sorafenib and lenvatinib, have been approved by the FDA for the treatment of radioactive-iodine refractory differentiated thyroid cancer. However, due to the adverse reactions and drug resistance caused by some targeted drugs, their application is limited. In response to targeted drug resistance and high rates of adverse reactions, research into new treatment combinations is being carried out; in addition to kinase inhibitor therapy, gene therapy and rutin-assisted iodine-131 therapy for radioactive-iodine refractory thyroid cancer have also made some progress. Thus, this article mainly focuses on sodium iodide symporter changes leading to the main molecular mechanisms in radioactive-iodine refractory differentiated thyroid cancer, some targeted drug resistance mechanisms and promising new treatments.
大多数分化型甲状腺癌患者在接受放射性碘-131 治疗后预后良好,但仍有少数患者对碘治疗不敏感,可能随后出现疾病进展。因此,放射性碘难治性分化型甲状腺癌经放射性碘治疗后通常表现为放射性碘摄取减少。因此,当钠碘同向转运体表达、基底外侧膜定位和再循环降解异常时,可能发生放射性碘难治性分化型甲状腺癌。近年来,随着对该病发病机制研究的深入,越来越多的分子成为或有望成为治疗靶点。针对不同分子靶点的相应抑制剂或联合治疗方案的应用,可能对晚期放射性碘难治性分化型甲状腺癌患者有效。目前,一些可改善放射性碘难治性分化型甲状腺癌患者无进展生存期的靶向药物,如索拉非尼和仑伐替尼,已被 FDA 批准用于治疗放射性碘难治性分化型甲状腺癌。然而,由于一些靶向药物引起的不良反应和耐药性,其应用受到限制。针对靶向药物耐药性和不良反应发生率高的问题,正在开展新的治疗组合研究;除了激酶抑制剂治疗外,基因治疗和芦丁辅助碘-131 治疗放射性碘难治性甲状腺癌也取得了一些进展。因此,本文主要关注导致放射性碘难治性分化型甲状腺癌的主要分子机制中的钠碘同向转运体变化、一些靶向药物耐药机制和有前途的新治疗方法。