摘要
Regorafenib(BAY73-4506)是一种口服多激酶抑制剂,可以靶向作用于血管源性、间质源性及致癌性等多种酪氨酸激酶。在体外及临床试验中Regorafenib均显示出显著的抗肿瘤活性。在恶性实体瘤特别是结直肠肿瘤的治疗中,Regorafenib的临床试验结果令人鼓舞。
Regorafenib, an oral muhi-kinase inhibitor, can inhabit a class of receptor tyrosine kinase, such as angiogenic, stromal, oncogenic and so on. Studies in vitro and clinical trials indicate that Regorafenib has significant antitumor activity. The results of clinical trials are encouraging for the treatment of Refractory solid tumors, especially for colorectal carcinoma.
出处
《国际肿瘤学杂志》
CAS
2013年第3期191-192,231,共3页
Journal of International Oncology
基金
基金项目:国家自然科学基金(81101551)
关键词
受体蛋白质酪氨酸激酶类
酶抑制剂
肿瘤
Receptor protein-tyrosine kinases
Enzyme inhibitors
Neoplasms