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综述文章:晚期分化型甲状腺癌的新治疗方法和耐药潜在机制。

Review article: new treatments for advanced differentiated thyroid cancers and potential mechanisms of drug resistance.

机构信息

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

出版信息

Front Endocrinol (Lausanne). 2023 Jun 26;14:1176731. doi: 10.3389/fendo.2023.1176731. eCollection 2023.

Abstract

The treatment of advanced, radioiodine refractory, differentiated thyroid cancers (RR-DTCs) has undergone major advancements in the last decade, causing a paradigm shift in the management and prognosis of these patients. Better understanding of the molecular drivers of tumorigenesis and access to next generation sequencing of tumors have led to the development and Food and Drug Administration (FDA)-approval of numerous targeted therapies for RR-DTCs, including antiangiogenic multikinase inhibitors, and more recently, fusion-specific kinase inhibitors such as RET inhibitors and NTRK inhibitors. BRAF + MEK inhibitors have also been approved for -mutated solid tumors and are routinely used in RR-DTCs in many centers. However, none of the currently available treatments are curative, and most patients will ultimately show progression. Current research efforts are therefore focused on identifying resistance mechanisms to tyrosine kinase inhibitors and ways to overcome them. Various novel treatment strategies are under investigation, including immunotherapy, redifferentiation therapy, and second-generation kinase inhibitors. In this review, we will discuss currently available drugs for advanced RR-DTCs, potential mechanisms of drug resistance and future therapeutic avenues.

摘要

在过去十年中,晚期、放射性碘难治性分化型甲状腺癌(RR-DTC)的治疗取得了重大进展,这导致了这些患者的治疗和预后发生了范式转变。对肿瘤发生的分子驱动因素的更好理解以及对肿瘤下一代测序的应用,导致了针对 RR-DTC 的许多靶向治疗药物的开发和美国食品和药物管理局(FDA)的批准,包括抗血管生成多激酶抑制剂,以及最近的融合特异性激酶抑制剂,如 RET 抑制剂和 NTRK 抑制剂。BRAF + MEK 抑制剂也已获准用于突变的实体瘤,并在许多中心常规用于 RR-DTC。然而,目前尚无治愈方法,大多数患者最终会出现进展。因此,目前的研究重点是确定对酪氨酸激酶抑制剂的耐药机制并寻找克服耐药性的方法。目前正在研究各种新的治疗策略,包括免疫疗法、再分化疗法和第二代激酶抑制剂。在这篇综述中,我们将讨论晚期 RR-DTC 的现有药物、潜在的耐药机制以及未来的治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6c/10331470/94e855a4a4a7/fendo-14-1176731-g001.jpg

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