摘要
舒尼替尼是一个小分子多靶点酪氨酸激酶抑制剂,可抑制多个与肿瘤生长和血管生成相关的受体酪氨酸激酶。2006年被FDA批准用于不能耐受伊马替尼或治疗后疾病进展的胃肠道问质瘤(GIST)患者。本文拟就舒尼替尼在胃肠道间质瘤二线治疗中可能的分子机制、耐药机制、生物标志物、临床试验、不良反应及局限性等方面作一综述。
Sunitinib malate (SU11248, Sutent) is an orally available small-molecule muhitargeted tyrosine kinase inhibitor that has potent anti-angiogenic and antitumour activities. In 2006 sunitinib was approved by FDA for imatinib intolerant gastrointestinal stromal tumors (GIST) patients or imatinib resistant GIST pa- tients. This article review the molecular-based mechanism, the mechanism of resistance,the hiomarker, the clinical trials and the adverse effects of sunitinib in the treatment of imatinib-resistant GIST.
出处
《国际外科学杂志》
2011年第2期132-135,共4页
International Journal of Surgery
关键词
舒尼替尼
胃肠道间质瘤
耐药
Sunitinib
Gastrointestinal stromal tumors
Resistance