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阿昔替尼(AG-013736)。

Axitinib (AG-013736).

作者信息

Kelly Ronan Joseph, Rixe Olivier

机构信息

Thoracic Oncology Department Medical Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

Recent Results Cancer Res. 2010;184:33-44. doi: 10.1007/978-3-642-01222-8_3.

Abstract

The vascular endothelial growth factor (VEGF)/VEGF receptor tyrosine kinase (RTK) signaling pathway plays a pivotal role in tumor angiogenesis. Neovascularization promotes increased tumor cell proliferation, survival and metasasis. Many antiangiogenic agents including multi-RTK inhibitors are either approved or are undergoing testing in clinical trials. Axitinib is a potent and selective inhibitor of VEGF RTK 1, 2, and 3. This chapter discusses the stucture of axitinib as well as its toxicities and drug interactions. Important preclinical and clinical data for axitinib are presented including findings from phase II studies in many tumor types including malignant melanoma and renal, pancreatic, thyroid, breast, lung and colorectal carcinomas. Ongoing phase III studies in pancreatic and metastatic renal cell carcinoma will ultimately define the therapeutic role of this targeted agent.

摘要

血管内皮生长因子(VEGF)/VEGF受体酪氨酸激酶(RTK)信号通路在肿瘤血管生成中起关键作用。新生血管形成促进肿瘤细胞增殖、存活和转移增加。许多抗血管生成药物,包括多RTK抑制剂,已获批准或正在进行临床试验。阿昔替尼是一种强效且选择性的VEGF RTK 1、2和3抑制剂。本章讨论了阿昔替尼的结构及其毒性和药物相互作用。还介绍了阿昔替尼重要的临床前和临床数据,包括在多种肿瘤类型(包括恶性黑色素瘤以及肾、胰腺、甲状腺、乳腺、肺和结肠直肠癌)的II期研究结果。正在进行的针对胰腺癌和转移性肾细胞癌的III期研究将最终确定这种靶向药物的治疗作用。

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