| Literature DB >> 31312646 |
Aline Gottlieb1, Jan Best1, Ali Canbay1.
Abstract
Hepatocellular carcinoma (HCC) remains one of the leading causes of cancer-related death worldwide. Upon ineligibility for resection, liver transplantation, or locoregional therapies, sorafenib has been the only systemic treatment option of advanced HCC for more than a decade. Immunotherapy is an evolving HCC treatment option that has shown promise in treatment efficacy at an acceptable safety profile during several preceding phase I/II trials. Numerous clinical trials of immune checkpoint inhibitors (ICPIs) alone, in combination of two, or combined with other targeted or locoregional therapies are ongoing. Encouraging results of two-phase III trials testing pembrolizumab or nivolumab versus standard care therapy even resulted in Food and Drug Administration approval for second-line treatment of advanced HCC. ICPIs may open new avenues to the treatment of hepatobiliary tumors, alone or in combination.Entities:
Keywords: Cytotoxic T-lymphocyte-associated protein 4 antibody; Hepatocellular carcinoma; Immune checkpoint inhibitors; Immunotherapy; Programmed cell death protein 1 antibody; Programmed death ligand 1 antibody; Targeted therapy
Year: 2019 PMID: 31312646 PMCID: PMC6597927 DOI: 10.1159/000496755
Source DB: PubMed Journal: Visc Med ISSN: 2297-4725