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治疗难治性甲状腺癌的新型分子靶向治疗药物。

Novel molecular targeted therapies for refractory thyroid cancer.

机构信息

Cleveland Clinic Florida, Weston, Florida, USA.

出版信息

Head Neck. 2012 May;34(5):736-45. doi: 10.1002/hed.21755. Epub 2011 May 4.

Abstract

The incidence of thyroid cancer continues to increase and this neoplasia remains the most common endocrine malignancy. No effective systemic treatment currently exists for iodine-refractory differentiated or medullary thyroid carcinoma, but recent advances in the pathogenesis of these diseases have revealed key targets that are now being evaluated in the clinical setting. RET (rearranged during transfection)/PTC (papillary thyroid carcinoma) gene rearrangements, B-Raf gene mutations, and vascular endothelial growth factor receptor 2 (VEGFR-2) angiogenesis pathways are some of the known genetic alterations playing a crucial role in the development of thyroid cancer. Several novel agents have demonstrated promising responses. Of the treatments studied, multi-kinase inhibitors such as axitinib, sorafenib, motesanib, and XL-184 have shown to be the most effective by inducing clinical responses and stabilizing the disease process. Randomized clinical trials are currently evaluating these agents, results that may soon change the management of thyroid cancer.

摘要

甲状腺癌的发病率持续上升,这种肿瘤仍然是最常见的内分泌恶性肿瘤。对于碘难治性分化型或髓样甲状腺癌,目前尚无有效的全身治疗方法,但这些疾病发病机制的最新进展揭示了一些关键靶点,目前正在临床评估中。RET(转染时重排)/PTC(甲状腺乳头状癌)基因重排、B-Raf 基因突变和血管内皮生长因子受体 2(VEGFR-2)血管生成途径是一些已知的遗传改变,在甲状腺癌的发展中起着至关重要的作用。一些新型药物已显示出有希望的反应。在研究的治疗方法中,多激酶抑制剂,如 axitinib、sorafenib、motesanib 和 XL-184,通过诱导临床反应和稳定疾病进程,显示出最有效的效果。目前正在进行随机临床试验来评估这些药物,这些结果可能很快会改变甲状腺癌的治疗方法。

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