晚期甲状腺癌难治碘的新靶点

Lynda Marianela Vásconez Proaño
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引用次数: 0

摘要

大多数因甲状腺癌导致的死亡发生在对放射性碘难治的晚期DTC患者中。近年来分子医学的惊人进展开辟了新的治疗可能性。目前,人们普遍认为,酪氨酸激酶抑制剂(TKI)治疗仅适用于对放射性碘难治的分化型甲状腺癌患者,以及无法局部治疗的进展性和/或有症状的转移性疾病。这些“新分子”大多是多通道抑制剂,具有多种作用,可作用于RET、BRAF、cKIT、MET、EGFR、MAPK、PDGFR等不同的蛋白。此外,它们还有一个额外的优势,即它们通过作用于VEGFR 1、2和3来显著阻止血管生成。TKI与无进展生存期相关,但不能治愈。此外,还会导致影响生活质量的不良影响。在两项III期试验中,与安慰剂相比,索拉非尼和lenvatinib可以延长无进展生存期。这两种药物已被FDA和欧洲药品管理局批准用于放射性碘难治性转移性疾病患者。基于II期试验,还有其他酪氨酸激酶抑制剂(TKI)可用,如舒尼替尼、阿西替尼或帕唑帕尼,它们可以产生某种临床益处,因此需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Targets in Advanced Thyroid Cancer Refractory Iodine
The majority of deaths due to thyroid cancer occur in patients with advanced DTC refractory to radioactive iodine. The spectacular advances in molecular medicine of recent years have opened new therapeutic possibilities. Currently, there is general agreement that treatment with Tyrosine Kinase Inhibitors (TKI) should only be considered in patients with differentiated thyroid carcinoma refractory to radioactive iodine, with progressive and / or symptomatic metastatic disease that can not otherwise be treated locally. Most of these "new molecules" are multichannel inhibitors with varied action, which interact on different proteins such as RET, BRAF, cKIT, MET, EGFR, MAPK, PDGFR, etc. In addition, they have the additional advantage that they markedly prevent angiogenesis by acting on VEGFR 1, 2, and 3. TKI are associated with progression-free survival but not curative. Also, causes adverse effects that can affect the quality of life.The prolongation of progression-free survival has been demonstrated with sorafenib and lenvatinib compared with placebo in two phase III trials. These two drugs have been approved by the FDA and the European Medicines Agency for use in patients refractory to radioactive iodine with metastatic disease. Based on the Phase II Trials there are other Tyrosine Kinase Inhibitors (TKI) available such as sunitinib, axitinib or pazopanib that can produce some kind of clinical benefit and therefore need further investigation.
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