Immune therapy for liver cancers Review


Authors: Hilmi, M.; Vienot, A.; Rousseau, B.; Neuzillet, C.
Review Title: Immune therapy for liver cancers
Abstract: Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) display a poor prognosis with 5-year overall survival rates around 15%, all stages taken together. These primary liver malignancies are often diagnosed at advanced stages where therapeutic options are limited. Recently, immune therapy has opened new opportunities in oncology. Based on their high programmed death-ligand 1 expression and tumor-infiltrating lymphocytes, HCC and BTC are theoretically good candidates for immune checkpoint blockade. However, clinical activity of single agent immunotherapy appears limited to a subset of patients, which is still ill-defined, and combinations are under investigation. In this review, we provide an overview of (i) the biological rationale for immunotherapies in HCC and BTC, (ii) the current state of their clinical development, and (iii) the predictive value of immune signatures for both clinical outcome and response to these therapies. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
Keywords: platelet derived growth factor; protein expression; overall survival; review; hepatocellular carcinoma; sorafenib; bevacizumab; fluorouracil; drug efficacy; drug safety; hypertension; liver cell carcinoma; liver dysfunction; gemcitabine; transcription factor foxp3; cd8+ t lymphocyte; ipilimumab; ticilimumab; unindexed drug; cancer immunotherapy; progression free survival; gene amplification; risk factor; risk assessment; scatter factor; oncogene; regulatory t lymphocyte; immunology; immune response; drug combination; folinic acid; immunogenicity; vasculotropin a; vaccinia virus; innate immunity; lymphocytic infiltration; axitinib; adaptive immunity; oxaliplatin; autoimmune disease; tumor vascularization; biliary tract cancer; biliary tract cancers; predictive value; programmed death 1 ligand 1; programmed death 1 receptor; tumor microenvironment; cancer associated fibroblast; tumor ablation; indoleamine 2,3 dioxygenase inhibitor; liver carcinogenesis; cancer prognosis; cabozantinib; nivolumab; regorafenib; lenvatinib; ramucirumab; human; checkpoint inhibitor; pembrolizumab; vegfa gene; durvalumab; atezolizumab; avelumab; cemiplimab; camrelizumab; rivoceranib; toripalimab
Journal Title: Cancers
Volume: 12
Issue: 1
ISSN: 2072-6694
Publisher: MDPI  
Date Published: 2020-01-01
Start Page: 77
Language: English
DOI: 10.3390/cancers12010077
PROVIDER: scopus
PUBMED: 31892230
PMCID: PMC7016834
DOI/URL:
Notes: Review -- Source: Scopus
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