医学
贝伐单抗
帕唑帕尼
舒尼替尼
肿瘤科
肾细胞癌
临床终点
内科学
索拉非尼
养生
替西罗莫司
临床试验
化疗
肝细胞癌
mTOR抑制剂的发现与发展
PI3K/AKT/mTOR通路
细胞凋亡
化学
生物化学
作者
Bohuslav Melichar,Hana Študentová,Denisa Vitásková
摘要
Metastatic renal cell carcinoma (mRCC) is tumor resistant to all cytotoxic agents. During the last decade, effective targeted therapies emerged including sunitinib, pazopanib and the combination of bevacizumab with IFN-α. The use of bevacizumab plus IFN-α combination in mRCC is supported by the AVOREN trial. Although the primary end point of the AVOREN trial was overall survival, progression-free survival was used to evaluate efficacy and served as the basis of regulatory submission owing to the advent of targeted agents that probably resulted in the prolongation of overall survival in both experimental and control arms. The doubling of median progression-free survival in the AVOREN trials (from 5.4 to 10.2 months) is remarkably similar compared with the results of Phase III trials with sunitinib and pazopanib. Bevacizumab plus IFN-α is the only combined regimen currently used in mRCC and serves as a comparator in the trials combining bevacizumab with other agents.
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