Progress in the treatment of advanced hepatocellular carcinoma with immune combination therapy

被引:6
作者
Pan, Di [1 ]
Liu, Hao-Nan [1 ]
Qu, Peng-Fei [2 ]
Ma, Xiao [1 ]
Ma, Lu-Yao [1 ]
Chen, Xiao-Xiao [1 ]
Wang, Yu-Qin [3 ]
Qin, Xiao-Bing [1 ]
Han, Zheng-Xiang [1 ,4 ]
机构
[1] Xuzhou Med Univ, Dept Oncol, Affiliated Hosp, Xuzhou 221000, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Dept Gastroenterol, Affiliated Hosp 2, Xuzhou 221000, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Dept Gen Surg, Affiliated Hosp, Xuzhou 221000, Jiangsu, Peoples R China
[4] Xuzhou Med Univ, Dept Oncol, Affiliated Hosp, 99 Huaihai West Rd, Xuzhou 221000, Jiangsu, Peoples R China
关键词
Hepatocellular carcinoma; Immunotherapies; Immune checkpoint inhibitor; Clinical efficacy; Adverse reactions; CABOZANTINIB PLUS ATEZOLIZUMAB; ARTERIAL INFUSION CHEMOTHERAPY; TRANSARTERIAL CHEMOEMBOLIZATION; OPEN-LABEL; PHASE-II; T-CELLS; SORAFENIB; LENVATINIB; IMMUNOTHERAPY; PEMBROLIZUMAB;
D O I
10.4251/wjgo.v16.i2.273
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advanced hepatocellular carcinoma (HCC) is a severe malignancy that poses a serious threat to human health. Owing to challenges in early diagnosis, most patients lose the opportunity for radical treatment when diagnosed. Nonetheless, recent advancements in cancer immunotherapy provide new directions for the treatment of HCC. For instance, monoclonal antibodies against immune checkpoint inhibitors (ICIs) such as programmed cell death protein 1/death ligand-1 inhibitors and cytotoxic t-lymphocyte associated antigen-4 significantly improved the prognosis of patients with HCC. However, tumor cells can evade the immune system through various mechanisms. With the rapid development of genetic engineering and molecular biology, various new immunotherapies have been used to treat HCC, including ICIs, chimeric antigen receptor T cells, engineered cytokines, and certain cancer vaccines. This review summarizes the current status, research progress, and future directions of different immunotherapy strategies in the treatment of HCC.
引用
收藏
页码:273 / 286
页数:15
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