Immune effect and prognosis of transcatheter arterial chemoembolization and tyrosine kinase inhibitors therapy in patients with hepatocellular carcinoma

被引:1
|
作者
Guo, Yuan [1 ]
Li, Ru-Chun [2 ]
Xia, Wei-Li [1 ]
Yang, Xiong [1 ]
Zhu, Wen-Bo [1 ]
Li, Fang-Ting [1 ]
Hu, Hong-Tao [1 ]
Li, Hai-Liang [1 ]
机构
[1] Zhengzhou Univ, Henan Canc Hosp, Dept Minimal Invas Intervent, Affiliated Canc Hosp, 127 Dongming Rd, Zhengzhou 450003, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Canc Hosp, Henan Canc Hosp, Dept Radiol, Zhengzhou 450003, Henan, Peoples R China
关键词
Transcatheter arterial chemoembolization; Hepatocellular carcinoma; Tyrosine kinase inhibitors; Immune microenvironment; Immune responses;
D O I
10.4251/wjgo.v16.i7.3256
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND The combination of transcatheter arterial chemoembolization (TACE) and tyrosine kinase inhibitors (TKIs) has shown broad prospects in prolonging the survival of patients with hepatocellular carcinoma (HCC). TACE and TKIs can affect the immune microenvironment in patients with HCC. AIM To determine the overall effects and differences between TACE and different TKIs combinations on the immune microenvironment. METHODS Data and immune cell profile test results from 213 HCC patients treated with TACE combined with apatinib, lenvatinib, sorafenib, or donafenib before and after 3 wk of treatment were collected. Monocytes were co-cultured with LM3 liver cancer cells, and their ability to inhibit cancer cell growth was analyzed using the MTT method and a nude mouse subcutaneous tumorigenesis experiment. Simulated combined therapy was done using an in situ liver cancer C57BL/6 male mouse model, and the immune response of tumor tissues was analyzed using immunohistochemistry. RESULTS Compared to before combination therapy, the proportion of programmed cell death protein 1 (PD-1)+ mononuclear cells and the number of CD4+ T cells decreased in the TACE + apatinib group, while the number of absolute count of CD4+ and CD8+ T cells increased in the TACE + lenvatinib group. Furthermore, the number of regulatory cells decreased in the TACE + donafenib group, whereas the number of CD8+ T and natural killer cells increased. Additionally, monocytes in the TACE combined with donafenib or lenvatinib groups had a stronger ability to inhibit cancer cell growth than those in the other groups. Combining TACE with donafenib or lenvatinib increased CD8+ T cell infiltration into the tumor tissue. In addition, the proportion of PD-1+ in CD8+ cells, absolute CD8+ T lymphocyte count, and regulatory T cells proportion were independent prognostic factors affecting the survival time of patients with HCC. CONCLUSION TACE, in combination with different TKIs, produces different immune responses. Specifically, TACE combined with donafenib or lenvatinib may induce strong anti-tumor immune responses.
引用
收藏
页数:15
相关论文
共 50 条
  • [11] Transcatheter arterial chemoembolization in hepatocellular carcinoma
    Farinati, F
    Rinaldi, M
    Gianni, S
    Marin, G
    HEPATOLOGY, 1998, 28 (05) : 1441 - 1442
  • [12] Effect of transcatheter arterial chemoembolization on cellular immune function and regulatory T cells in patients with hepatocellular carcinoma
    Liao, Juan
    Xiao, Jiangwei
    Zhou, Yunfeng
    Liu, Zilin
    Wang, Chunhui
    MOLECULAR MEDICINE REPORTS, 2015, 12 (04) : 6065 - 6071
  • [13] Safety and Efficacy of Transarterial Chemoembolization Combined With Immune Checkpoint Inhibitors and Tyrosine Kinase Inhibitors for Hepatocellular Carcinoma
    Yang, Fei
    Yang, Jun
    Xiang, Wei
    Zhong, Bin-Yan
    Li, Wan-Ci
    Shen, Jian
    Zhang, Shuai
    Yin, Yu
    Sun, Hong-Peng
    Wang, Wan-Sheng
    Zhu, Xiao-Li
    FRONTIERS IN ONCOLOGY, 2022, 11
  • [14] Effect of segmental transcatheter arterial chemoembolization on branched chain amino acids and tyrosine ratio in patients with hepatocellular carcinoma
    Inoue, K
    Ito, T
    Siraki, K
    Sugimoto, K
    Sakai, T
    Oomori, S
    Takase, K
    Nakano, T
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2000, 17 (05) : 977 - 980
  • [15] Transarterial Chemoembolization Combined with Immune Checkpoint Inhibitors Plus Tyrosine Kinase Inhibitors versus Immune Checkpoint Inhibitors Plus Tyrosine Kinase Inhibitors for Advanced Hepatocellular Carcinoma
    Huang, Jin-Tao
    Zhong, Bin-Yan
    Jiang, Nan
    Li, Wan-Ci
    Zhang, Shuai
    Yin, Yu
    Yang, Jun
    Shen, Jian
    Wang, Wan-Sheng
    Zhu, Xiao-Li
    JOURNAL OF HEPATOCELLULAR CARCINOMA, 2022, 9 : 1217 - 1228
  • [16] Transcatheter arterial chemoembolization therapy for patients with hepatocellular carcinoma:: A case-controlled study
    Biselli, M
    Andreone, P
    Gramenzi, A
    Trevisani, F
    Cursaro, C
    Rossi, C
    Rosellino, SR
    Cammà, C
    Lorenzini, S
    Stefanini, GF
    Gasbarrini, G
    Bernardi, M
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2005, 3 (09) : 918 - 925
  • [17] Transcatheter arterial chemoembolization therapy for patients with, hepatocellular carcinoma (HCC): A controlled trial.
    Biselli, M
    Gramenzi, A
    Stefanini, GF
    Trevisani, F
    Camma, C
    Rossellini, SR
    Cursaro, C
    Lorenzini, S
    Gasbarrini, G
    Bernardi, M
    HEPATOLOGY, 2002, 36 (04) : 395A - 395A
  • [18] Ketone bodies as a predictor of prognosis of hepatocellular carcinoma after transcatheter arterial chemoembolization
    Sasaki, Ryu
    Taura, Naota
    Miyazoe, Yuri
    Yamamichi, Shinobu
    Nakashiki, Suguru
    Yamashima, Mio
    Suehiro, Tomoyuki
    Honda, Takuya
    Shibata, Hidetaka
    Ozawa, Eisuke
    Miuma, Satoshi
    Akazawa, Yuko
    Miyaaki, Hisamitsu
    Matsumoto, Takehiro
    Nakao, Kazuhiko
    Ashizawa, Kazuto
    NUTRITION, 2018, 50 : 97 - 103
  • [19] TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION FOR HEPATOCELLULAR-CARCINOMA
    YANG, CF
    HO, YZ
    CHANG, JM
    CHIANG, RH
    LAI, KH
    LEE, SD
    TSAI, YT
    LUI, WY
    LIU, TJ
    CHEN, GH
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1989, 23 : S26 - S28
  • [20] Transcatheter arterial chemoembolization in hepatocellular carcinoma - Reply
    Llovet, JM
    Castells, A
    Bruix, J
    HEPATOLOGY, 1998, 28 (05) : 1442 - 1443