Motzer Robert J, Hoosen Sakina, Bello Carlo L, Christensen James G
Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Expert Opin Investig Drugs. 2006 May;15(5):553-61. doi: 10.1517/13543784.15.5.553.
Receptor tyrosine kinases (RTKs) play important roles in the regulation of cellular growth, and mutated or overexpressed RTKs have been implicated in various human cancers. Sunitinib malate is an oral multitargeted tyrosine kinase inhibitor with antitumour and antiangiogenic activity that recently received approval from the FDA for the treatment of advanced renal cell carcinoma and of gastrointestinal stromal tumours after disease progression on or intolerance to imatinib mesilate therapy. Sunitinib has also demonstrated promising clinical activity in the treatment of other advanced solid tumours. The present review provides an updated summary of emerging clinical experience with this promising new anticancer agent.
受体酪氨酸激酶(RTKs)在细胞生长调节中发挥重要作用,RTKs的突变或过表达与多种人类癌症有关。苹果酸舒尼替尼是一种口服多靶点酪氨酸激酶抑制剂,具有抗肿瘤和抗血管生成活性,最近获得美国食品药品监督管理局(FDA)批准,用于治疗晚期肾细胞癌以及在接受甲磺酸伊马替尼治疗后病情进展或不耐受的胃肠道间质瘤。舒尼替尼在治疗其他晚期实体瘤方面也显示出有前景的临床活性。本综述提供了这种有前景的新型抗癌药物新出现的临床经验的最新总结。