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分子遗传学、治疗学和 RET 抑制剂耐药性在甲状腺髓样癌中的应用及未来展望。

Molecular genetics, therapeutics and RET inhibitor resistance for medullary thyroid carcinoma and future perspectives.

机构信息

Department of Thyroid Surgery, Zhejiang Cancer Hospital, No. 1 East Banshan Road, Gongshu District, Hangzhou, 310022, Zhejiang, China.

Department of Radiation Oncology, Shanghai Pulmonary Hospital, Tongji University Medical School Cancer Institute, Tongji University School of Medicine, Shanghai, China.

出版信息

Cell Commun Signal. 2024 Sep 28;22(1):460. doi: 10.1186/s12964-024-01837-x.

Abstract

Medullary thyroid carcinoma (MTC) is a rare type of thyroid malignancy that accounts for approximately 1-2% of all thyroid cancers (TCs). MTC include hereditary and sporadic cases, the former derived from a germline mutation of rearrangement during transfection (RET) proto-oncogene, whereas somatic RET mutations are frequently present in the latter. Surgery is the standard treatment for early stage MTC, and the 10-year survival rate of early MTC is over 80%. While for metastatic MTC, chemotherapy showing low response rate, and there was a lack of effective systemic therapies in the past. Due to the high risk (ca. 15-20%) of distant metastasis and limited systemic therapies, the 10-year survival rate of patients with advanced MTC was only 10-40% from the time of first metastasis. Over the past decade, targeted therapy for RET has developed rapidly, bringing hopes to patients with advanced and progressive MTC. Two multi-kinase inhibitors (MKIs) including Cabozantinib and Vandetanib have been shown to increase progression-free survival (PFS) for patients with metastatic MTC and have been approved as choices of first-line treatment. However, these MKIs have not prolonged overall survival (OS) and their utility is limited due to high rates of off-target toxicities. Recently, new generation TKIs, including Selpercatinib and Pralsetinib, have demonstrated highly selective efficacy against RET and more favorable side effect profiles, and gained approval as second-line treatment options. Despite the ongoing development of RET inhibitors, the management of advanced and progressive MTC remains challenging, drug resistance remains the main reason for treatment failure, and the mechanisms are still unclear. Besides, new promising therapeutic approaches, such as novel drug combinations and next generation RET inhibitors are under development. Herein, we overview the pathogenesis, molecular genetics and current management approaches of MTC, and focus on the recent advances of RET inhibitors, summarize the current situation and unmet needs of these RET inhibitors in MTC, and provide an overview of novel strategies for optimizing therapeutic effects.

摘要

甲状腺髓样癌(MTC)是一种罕见的甲状腺恶性肿瘤,约占所有甲状腺癌(TCs)的 1-2%。MTC 包括遗传性和散发性病例,前者来源于转染过程中重排的 RET 原癌基因突变,而后者常存在体细胞 RET 突变。手术是治疗早期 MTC 的标准方法,早期 MTC 的 10 年生存率超过 80%。对于转移性 MTC,化疗反应率低,过去缺乏有效的全身治疗方法。由于远处转移的高风险(约 15-20%)和有限的全身治疗方法,首次转移后,晚期 MTC 患者的 10 年生存率仅为 10-40%。在过去的十年中,RET 的靶向治疗发展迅速,为晚期和进展性 MTC 患者带来了希望。两种多激酶抑制剂(MKIs)包括卡博替尼和凡德他尼已被证明可延长转移性 MTC 患者的无进展生存期(PFS),并被批准为一线治疗选择。然而,由于脱靶毒性发生率高,这些 MKIs 并未延长总生存期(OS),其应用受到限制。最近,新一代 TKI,包括塞尔帕替尼和普拉替尼,已证明对 RET 具有高度选择性疗效和更有利的副作用谱,并获得批准作为二线治疗选择。尽管 RET 抑制剂的研发正在进行中,但晚期和进展性 MTC 的治疗仍然具有挑战性,耐药性仍然是治疗失败的主要原因,其机制仍不清楚。此外,新的有前途的治疗方法,如新型药物组合和下一代 RET 抑制剂正在开发中。本文综述了 MTC 的发病机制、分子遗传学和当前的治疗方法,重点介绍了 RET 抑制剂的最新进展,总结了这些 RET 抑制剂在 MTC 中的现状和未满足的需求,并概述了优化治疗效果的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fa0/11439284/cab88537b8c2/12964_2024_1837_Fig1_HTML.jpg

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