Immune Checkpoint Inhibitors in Hepatocellular Carcinoma: Opportunities and Challenges

被引:108
作者
Liu, Xiufeng [1 ]
Qin, Shukui [1 ]
机构
[1] Nanjing Univ Chinese Med, Bayi Hosp, Peoples Liberat Army Canc Ctr, Nanjing 21002, Jiangsu, Peoples R China
关键词
Immune checkpoint inhibitors; Hepatocellular carcinoma; Combinatorial immunotherapy strategies; Underlying liver disease; Hepatitis B virus; PROGRAMMED DEATH LIGAND-1; T-REGULATORY CELLS; HEPATITIS-B-VIRUS; RADIOFREQUENCY ABLATION; OPEN-LABEL; SORAFENIB RESISTANCE; ANTITUMOR ACTIVITIES; SYSTEMIC THERAPY; PD-L1; EXPRESSION; MULTICENTER;
D O I
10.1634/theoncologist.2019-IO-S1-s01
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is the most common malignancy worldwide, and is especially common in China. A total of 70%-80% of patients are diagnosed at an advanced stage and can receive only palliative care. Sorafenib has been the standard of care for a decade, and promising results for regorafenib as a second-line and lenvatinib as a first-line treatment were reported only 1 or 2 years ago. FOLFOX4 was recently recommended as a clinical practice guideline by the China Food and Drug Administration. All approved systemic therapies remain unsatisfactory, with limited objective response rates and poor overall survival. Immune checkpoint inhibitors (CPIs) offer great promise in the treatment of a rapidly expanding spectrum of solid tumors. Immune checkpoint molecules are involved in almost the whole process of viral-related hepatitis with cirrhosis and HCC and in the most important resistance mechanism of sorafenib. The approval of nivolumab by the U.S. Food and Drug Administration on September 23, 2017, for the treatment of patients with HCC, based only on a phase I/II clinical trial, is a strong hint that immunotherapy will introduce a new era of HCC therapy. CPI-based strategies will soon be a main approach in anticancer treatment for HCC, and we will observe the rapid advances in the therapeutic use of CPIs, even in an adjuvant setting, with great interest. How shall we face the opportunities and challenges? Can we dramatically improve the prognosis of patients with HCC? This review may provide some informed guidance.
引用
收藏
页码:S3 / S10
页数:8
相关论文
共 79 条
[1]   Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma [J].
Ally, Adrian ;
Balasundaram, Miruna ;
Carlsen, Rebecca ;
Chuah, Eric ;
Clarke, Amanda ;
Dhalla, Noreen ;
Holt, Robert A. ;
Jones, Steven J. M. ;
Lee, Darlene ;
Ma, Yussanne ;
Marra, Marco A. ;
Mayo, Michael ;
Moore, Richard A. ;
Mungall, Andrew J. ;
Schein, Jacqueline E. ;
Sipahimalani, Payal ;
Tam, Angela ;
Thiessen, Nina ;
Cheung, Dorothy ;
Wong, Tina ;
Brooks, Denise ;
Robertson, A. Gordon ;
Bowlby, Reanne ;
Mungall, Karen ;
Sadeghi, Sara ;
Xi, Liu ;
Covington, Kyle ;
Shinbrot, Eve ;
Wheeler, David A. ;
Gibbs, Richard A. ;
Donehower, Lawrence A. ;
Wang, Linghua ;
Bowen, Jay ;
Gastier-Foster, Julie M. ;
Gerken, Mark ;
Helsel, Carmen ;
Leraas, Kristen M. ;
Lichtenberg, Tara M. ;
Ramirez, Nilsa C. ;
Wise, Lisa ;
Zmuda, Erik ;
Gabriel, Stacey B. ;
Meyerson, Matthew ;
Cibulskis, Carrie ;
Murray, Bradley A. ;
Shih, Juliann ;
Beroukhim, Rameen ;
Cherniack, Andrew D. ;
Schumacher, Steven E. ;
Saksena, Gordon .
CELL, 2017, 169 (07) :1327-+
[2]  
[Anonymous], 2017, P AM SOC CLIN ONCOL
[3]  
[Anonymous], 2018, J CLIN ONCOL
[4]  
[Anonymous], J CLIN ONCOL S15
[5]  
[Anonymous], CHIN CLIN ONCOL
[6]  
[Anonymous], ANN ONCOL S5
[7]  
[Anonymous], LANCET ONCOL
[8]  
[Anonymous], J CLIN ONCOL S15
[9]   Unmasking of α-fetoprotein-specific CD4+ T cell responses in hepatocellular carcinoma patients undergoing embolization [J].
Ayaru, Lakshmana ;
Pereira, Stephen P. ;
Alisa, Akeel ;
Pathan, Ansar A. ;
Williams, Roger ;
Davidson, Brian ;
Burroughs, Andrew K. ;
Meyer, Tim ;
Behboudi, Shahriar .
JOURNAL OF IMMUNOLOGY, 2007, 178 (03) :1914-1922
[10]   Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer [J].
Borghaei, H. ;
Paz-Ares, L. ;
Horn, L. ;
Spigel, D. R. ;
Steins, M. ;
Ready, N. E. ;
Chow, L. Q. ;
Vokes, E. E. ;
Felip, E. ;
Holgado, E. ;
Barlesi, F. ;
Kohlhaeufl, M. ;
Arrieta, O. ;
Burgio, M. A. ;
Fayette, J. ;
Lena, H. ;
Poddubskaya, E. ;
Gerber, D. E. ;
Gettinger, S. N. ;
Rudin, C. M. ;
Rizvi, N. ;
Crino, L. ;
Blumenschein, G. R. ;
Antonia, S. J. ;
Dorange, C. ;
Harbison, C. T. ;
Finckenstein, F. Graf ;
Brahmer, J. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) :1627-1639