医学
阿替唑单抗
贝伐单抗
肝细胞癌
肿瘤科
背景(考古学)
内科学
癌症
药代动力学
免疫疗法
化疗
无容量
生物
古生物学
作者
Xiufeng Liu,Yi Lu,Shukui Qin
出处
期刊:Future Oncology
[Future Medicine]
日期:2021-03-05
卷期号:17 (17): 2243-2256
被引量:49
标识
DOI:10.2217/fon-2020-1290
摘要
Hepatocellular carcinoma (HCC) is a common cancer globally and a leading cause of cancer-related deaths. Although early-stage disease may be curable by resection, liver transplantation or ablation, many patients present with unresectable disease and have a poor prognosis. Combination treatment with atezolizumab (targeting PD-L1) and bevacizumab (targeting VEGF) in the recent IMbrave150 study was shown to be effective with an acceptable safety profile in patients with unresectable HCC. Herein, we discuss this novel combination in the context of the liver immune environment, summarize the mechanism and pharmacokinetics of atezolizumab and bevacizumab, and examine recent data on other immune checkpoint inhibitor combination strategies as well as future directions in the treatment of patients with advanced HCC.
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