无容量
阿替唑单抗
内科学
肿瘤科
彭布罗利珠单抗
肿瘤微环境
肝癌
伦瓦提尼
杜瓦卢马布
程序性细胞死亡1
化疗
作者
Zuzana Macek Jilkova,Caroline Aspord,Thomas Decaens
出处
期刊:Cancers
[MDPI AG]
日期:2019-10-14
卷期号:11 (10): 1554-1554
被引量:67
标识
DOI:10.3390/cancers11101554
摘要
Immunotherapies targeting immune checkpoints are fast-developing therapeutic approaches adopted for several tumor types that trigger unprecedented rates of durable clinical responses. Immune checkpoint programmed cell death protein 1 (PD-1), expressed primarily by T cells, and programmed cell death ligand 1 (PD-L1), expressed mainly by tumor cells, macrophages, and dendritic cells, are molecules that impede immune function, thereby allowing tumor cells to proliferate, grow and spread. PD-1/PD-L1 checkpoint inhibitors have emerged as a promising treatment strategy of hepatocellular carcinoma (HCC). However, only a minority of HCC patients benefit from this therapy. To find a niche for immune checkpoint inhibition in HCC patients, future strategies might require predictive factor-based patient selection, to identify patients who are likely to respond to the said therapy and combination strategies in order to enhance anti-tumor efficacy and clinical success. This review provides an overview of the most recent data pertaining to predictive factors for response to PD-1/PD-L1 checkpoint inhibition in the field of HCC.
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