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索拉非尼:晚期肾细胞癌患者单药及与α-干扰素联合应用活性的最新进展

Sorafenib: recent update on activity as a single agent and in combination with interferon-alpha2 in patients with advanced-stage renal cell carcinoma.

作者信息

Reddy G Kesava, Bukowski Ronald M

机构信息

CIG Media Group, LP, Dallas, TX, USA.

出版信息

Clin Genitourin Cancer. 2006 Mar;4(4):246-8. doi: 10.3816/cgc.2006.n.002.

Abstract

Metastatic renal cell carcinoma does not respond favorably to conventional treatment strategies and is not very responsive to cytokine therapy. Therefore, novel targeted treatment approaches have been explored for patients with renal cancer who have chemotherapy-refractory disease. Sorafenib (BAY 43-9006) is a small-molecule inhibitor that has been shown to target members of multiple classes of tyrosine kinases that are known to be involved in tumor cell proliferation and tumor angiogenesis. These kinases include vascular endothelial growth factor receptor (VEGFR)-1, VEGFR-2, VEGFR-3, platelet-derived growth factor receptor, Flt-3, c-kit, and Raf kinases. Based on the significant improvement in progression-free survival, sorafenib received Food and Drug Administration approval in December 2005 for the treatment of renal cell carcinoma. In combination studies, sorafenib with other antitumor agents has demonstrated significant clinical activity in patients with renal cell carcinoma. As discussed in this mini-review, the clinical potency of sorafenib as a single agent or in combination with other antitumor agents is being evaluated in several ongoing clinical trials in patients with renal carcinoma.

摘要

转移性肾细胞癌对传统治疗策略反应不佳,对细胞因子治疗也不太敏感。因此,对于患有化疗难治性疾病的肾癌患者,人们探索了新的靶向治疗方法。索拉非尼(BAY 43 - 9006)是一种小分子抑制剂,已被证明可靶向多种已知参与肿瘤细胞增殖和肿瘤血管生成的酪氨酸激酶。这些激酶包括血管内皮生长因子受体(VEGFR)-1、VEGFR-2、VEGFR-3、血小板衍生生长因子受体、Flt-3、c-kit和Raf激酶。基于无进展生存期的显著改善,索拉非尼于2005年12月获得美国食品药品监督管理局批准用于治疗肾细胞癌。在联合研究中,索拉非尼与其他抗肿瘤药物已在肾细胞癌患者中显示出显著的临床活性。如本综述所述,索拉非尼作为单一药物或与其他抗肿瘤药物联合使用的临床疗效正在针对肾癌患者的多项正在进行的临床试验中进行评估。

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