| Literature DB >> 33271389 |
Eleonora Lai1, Giorgio Astara2, Pina Ziranu3, Andrea Pretta4, Marco Migliari5, Marco Dubois6, Clelia Donisi7, Stefano Mariani8, Nicole Liscia9, Valentino Impera10, Mara Persano11, Simona Tolu12, Francesca Balconi13, Giovanna Pinna14, Dario Spanu15, Annagrazia Pireddu16, Giorgio Saba17, Silvia Camera18, Francesca Musio19, Marco Puzzoni20, Valeria Pusceddu21, Clelia Madeddu22, Andrea Casadei Gardini23, Mario Scartozzi24.
Abstract
Advanced hepatocellular carcinoma (HCC) is the most frequent liver cancer. Immunotherapy has been explored in this disease in order to improve survival outcomes. Nowadays, scientific research is focusing especially on immune checkpoint inhibitors, in particular anti-PD1, anti-PD-L1 and anti-CTLA4 monoclonal antibodies (mAbs), as single-agent or in combination with other immunotherapy agents, target therapies, anti-vascular endothelial growth factor (VEGF) and other agents targeting specific molecular pathways. Other immunotherapy strategies have been assessed or are under investigation in advanced HCC, namely cytokines, adoptive cell therapy, oncolytic virus, cancer vaccines. Each treatment presents specific efficacy and toxicity profiles, strictly related to their mechanism of action and to advanced HCC tumour microenvironment (TME). The aim of this review is to outline the state-of-the-art of immunotherapy in advanced HCC treatment, highlighting data on already investigated treatment strategies, safety and toxicity (including HBV/HCV-related HCC), and ongoing clinical trials focusing on new promising therapeutic weapons.Entities:
Keywords: Adoptive cell transfer; Advanced hepatocellular carcinoma; Cytokines; Immune checkpoint inhibitors; Immune-related toxicity; Oncolytic virus; Vaccines
Year: 2020 PMID: 33271389 DOI: 10.1016/j.critrevonc.2020.103167
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312