Advances in immunotherapy for hepatocellular carcinoma

被引:948
作者
Sangro, Bruno [1 ,2 ,3 ]
Sarobe, Pablo [4 ]
Hervas-Stubbs, Sandra [4 ]
Melero, Ignacio [4 ,5 ]
机构
[1] Clin Univ Navarra IDISNA, Liver Unit, Pamplona, Spain
[2] Clin Univ Navarra IDISNA, HPB Oncol Area, Pamplona, Spain
[3] CIBEREHD, Pamplona, Spain
[4] CIMA Univ Navarra, Program Immunol & Immunotherapy, IDISNA, Pamplona, Spain
[5] Clin Univ Navarra IDISNA, Dept Immunol & Immunotherapy, Pamplona, Spain
基金
欧盟地平线“2020”;
关键词
REGULATORY T-CELLS; HEPATIC STELLATE CELLS; SUPPRESSOR-CELLS; DOUBLE-BLIND; TRANSFORMING GROWTH-FACTOR-BETA-1; PERIPHERAL-BLOOD; POOR-PROGNOSIS; KILLER-CELLS; PATIENTS PTS; ADOPTIVE IMMUNOTHERAPY;
D O I
10.1038/s41575-021-00438-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Immunotherapeutic interventions might be effective tools for the treatment of hepatocellular carcinoma. This Review provides up-to-date information on the clinical use of currently available immunotherapies in hepatocellular carcinoma, the mechanisms of response and resistance, and the therapeutic strategies under development. Hepatocellular carcinoma (HCC) is a prevalent disease with a progression that is modulated by the immune system. Systemic therapy is used in the advanced stage and until 2017 consisted only of antiangiogenic tyrosine kinase inhibitors (TKIs). Immunotherapy with checkpoint inhibitors has shown strong anti-tumour activity in a subset of patients and the combination of the anti-PDL1 antibody atezolizumab and the VEGF-neutralizing antibody bevacizumab has or will soon become the standard of care as a first-line therapy for HCC, whereas the anti-PD1 agents nivolumab and pembrolizumab are used after TKIs in several regions. Other immune strategies such as adoptive T-cell transfer, vaccination or virotherapy have not yet demonstrated consistent clinical activity. Major unmet challenges in HCC checkpoint immunotherapy are the discovery and validation of predictive biomarkers, advancing treatment to earlier stages of the disease, applying the treatment to patients with liver dysfunction and the discovery of more effective combinatorial or sequential approaches. Combinations with other systemic or local treatments are perceived as the most promising opportunities in HCC and some are already under evaluation in large-scale clinical trials. This Review provides up-to-date information on the best use of currently available immunotherapies in HCC and the therapeutic strategies under development.
引用
收藏
页码:525 / 543
页数:19
相关论文
共 212 条
[81]   Human and Mouse VEGFA-Amplified Hepatocellular Carcinomas Are Highly Sensitive to Sorafenib Treatment [J].
Horwitz, Elad ;
Stein, Ilan ;
Andreozzi, Mariacarla ;
Nemeth, Julia ;
Shoham, Avivit ;
Pappo, Orit ;
Schweitzer, Nora ;
Tornillo, Luigi ;
Kanarek, Naama ;
Quagliata, Luca ;
Zreik, Farid ;
Porat, Rinnat M. ;
Finkelstein, Rutie ;
Reuter, Hendrik ;
Koschny, Ronald ;
Ganten, Tom ;
Mogler, Carolin ;
Shibolet, Oren ;
Hess, Jochen ;
Breuhahn, Kai ;
Grunewald, Myriam ;
Schirmacher, Peter ;
Vogel, Arndt ;
Terracciano, Luigi ;
Angel, Peter ;
Ben-Neriah, Yinon ;
Pikarsky, Eli .
CANCER DISCOVERY, 2014, 4 (06) :730-743
[82]   Towards personalized, tumour-specific, therapeutic vaccines for cancer [J].
Hu, Zhuting ;
Ott, Patrick A. ;
Wu, Catherine J. .
NATURE REVIEWS IMMUNOLOGY, 2018, 18 (03) :168-182
[83]   Dual function of CTLA-4 in regulatory T cells and conventional T cells to prevent multiorgan autoimmunity [J].
Jain, Nitya ;
Nguyen, Hai ;
Chambers, Cynthia ;
Kang, Joonsoo .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (04) :1524-1528
[84]   Hepatic stellate cell and monocyte interaction contributes to poor prognosis in hepatocellular carcinoma [J].
Ji, Juling ;
Eggert, Tobias ;
Budhu, Anuradha ;
Forgues, Marshonna ;
Takai, Atsushi ;
Dang, Hien ;
Ye, Qinghai ;
Lee, Ju-Seog ;
Kim, Ji Hoon ;
Greten, Tim F. ;
Wang, Xin Wei .
HEPATOLOGY, 2015, 62 (02) :481-495
[85]   Signatures of T cell dysfunction and exclusion predict cancer immunotherapy response [J].
Jiang, Peng ;
Gu, Shengqing ;
Pan, Deng ;
Fu, Jingxin ;
Sahu, Avinash ;
Hu, Xihao ;
Li, Ziyi ;
Traugh, Nicole ;
Bu, Xia ;
Li, Bo ;
Liu, Jun ;
Freeman, Gordon J. ;
Brown, Myles A. ;
Wucherpfennig, Kai W. ;
Liu, X. Shirley .
NATURE MEDICINE, 2018, 24 (10) :1550-+
[86]   A phase I clinical trial utilizing autologous tumor-infiltrating lymphocytes in patients with primary hepatocellular carcinoma [J].
Jiang, Shan-Shan ;
Tang, Yan ;
Zhang, Yao-Jun ;
Weng, De-Sheng ;
Zhou, Zhong-Guo ;
Pan, Ke ;
Pan, Qiu-Zhong ;
Wang, Qi-Jing ;
Liu, Qing ;
He, Jia ;
Zhao, Jing-Jing ;
Li, Jiang ;
Chen, Min-Shan ;
Chang, Alfred E. ;
Li, Qiao ;
Xia, Jian-Chuan .
ONCOTARGET, 2015, 6 (38) :41339-41349
[87]   Anti-GPEC3-CAR T Cells Suppress the Growth of Tumor Cells in Patient-Derived Xenogratfts of Hepatocelluar Carcinoma [J].
Jiang, Zhiwu ;
Jiang, Xiaofeng ;
Chen, Suimin ;
Lai, Yunxin ;
Wei, Xinru ;
Li, Baiheng ;
Lin, Simiao ;
Wang, Suna ;
Wu, Qiting ;
Liang, Qiubin ;
Liu, Qifa ;
Peng, Muyun ;
Yu, Fenglei ;
Weng, Jianyu ;
Du, Xin ;
Pei, Duanqing ;
Liu, Pentao ;
Yao, Yao ;
Xue, Ping ;
Li, Peng .
FRONTIERS IN IMMUNOLOGY, 2017, 7
[88]   Chimeric Antigen Receptor Therapy [J].
June, Carl H. ;
Sadelain, Michel .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (01) :64-73
[89]   Reduced NKG2D ligand expression in hepatocellular carcinoma correlates with early recurrence [J].
Kamimura, Hiroteru ;
Yamagiwa, Satoshi ;
Tsuchiya, Atsunori ;
Takamura, Masaaki ;
Matsuda, Yasunobu ;
Ohkoshi, Shogo ;
Inoue, Makoto ;
Wakai, Toshifumi ;
Shirai, Yoshio ;
Nomoto, Minoru ;
Aoyagi, Yutaka .
JOURNAL OF HEPATOLOGY, 2012, 56 (02) :381-388
[90]  
Kelley RK, 2020, J CLIN ONCOL, V38