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Imaging of Metastatic Clear Cell Renal Cell Carcinoma: Objectifying Imaging Changes Post-TKI

机译:转移性透明细胞肾细胞癌的成像:TKI后的成像变化

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The National Cancer Institute estimates that 64,770 new cases and 13,570 deaths from kidney cancer in the United States occurred in 2012. Though a greater number of incidentally detected renal tumors are at a stage where surgery is curative, renal cell carcinoma (RCC) remains a clinically occult tumor, with up to one-third of patients presenting with advanced stage, harboring a 5-year survival rate of about 20%. The elucidation of the cytogenetic mechanism of hypoxia-inducible factor alpha cascade and VHL suppressor gene in the development of clear cell RCC has led to the discovery of various vascular endothelial growth factor-targeted therapy agents (also known as tyrosine kinase inhibitors [TKIs]) in treatment of metastatic clear cell renal cell carcinoma (mRCC). As with patients with other vascular tumors treated with targeted therapy, such as metastatic gastrointestinal stromal tumor with imitanib, TKI-treated patients treated with mRCC have an improved response and survival when compared to those treated with conventional chemotherapy (CT). Sunitinib and sorafenib are two such biologic agents that have been approved as first-line therapy for clear cell mRCC. These antiangiogenic TKIs exhibit both cyto-toxic and cytostatic properties and cause tumor regression and tumor growth suppression.
机译:国家癌症研究所估计,2012年患有64,770例新案件和来自美国肾癌的13,570人死亡。虽然更多的偶然检测到的肾脏肿瘤是在手术治疗的阶段,但肾细胞癌(RCC)仍然是临床隐匿性肿瘤,最多三分之一的患者患有高级阶段,含有5年生存率约为20%。缺氧诱导因子α级联和VHL抑制基因在透明细胞RCC发育中的细胞遗传学机制的阐明导致了各种血管内皮生长因子靶向治疗剂的发现(也称为酪氨酸激酶抑制剂[TKIS])治疗转移性透明细胞肾细胞癌(MRCC)。与用靶向治疗处理的其他血管肿瘤的患者一样,与含有IMITANIB的转移性胃肠肿瘤,与用常规化疗(CT)处理的人相比,使用MRCC处理的TKI治疗的患者具有改善的反应和存活。 Sunitinib和Sorafenib是两种这样的生物制剂,被批准为透明细胞MRCC的一线治疗。这些抗血管生成的TKI具有细胞毒性和细胞抑制性质,并引起肿瘤回归和肿瘤生长抑制。

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