| Literature DB >> 33259135 |
Ayano Kabashima1, Shu Shimada1, Masahiro Shimokawa1, Yoshimitsu Akiyama1, Minoru Tanabe2, Shinji Tanaka1,2.
Abstract
The development of hepatocellular carcinoma (HCC) is a multistep process with a complex interaction of various genetic backgrounds and the tumor microenvironment. In addition to the development of rational approaches to epidemiologic research, early detection, and diagnosis, considerable progress has been made in systemic treatment with molecular-targeted agents for patients with advanced HCC. Moreover, encouraging reports of recent clinical trials of combination therapy with immune-checkpoint inhibitors (ICIs) has raised high hopes. Each HCC is the result of a unique combination of somatic alterations, including genetic, epigenetic, transcriptomic, and metabolic events, leading to conclusive tumoral heterogeneity. Recent advances in comprehensive genetic analysis have accelerated molecular classification and defined subtypes with specific characteristics, including immune-associated molecular profiles reflecting the immune reactivity in the tumor. In considering the development of therapeutic strategies in combination with immunotherapy, proper interpretation of molecular pathological characterization could lead to effective therapeutic deployment and enable individualization of the management of HCC. Here, we review distinctive molecular alterations in the subtype classification of HCC, current therapies, and representative clinical trials with alternative immune-combination approaches from a molecular pathological point. This article is protected by copyright. All rights reserved.Entities:
Keywords: combination therapy; hepatocellular carcinoma; immunotherapy; molecular targeted therapy; subclass classification
Year: 2020 PMID: 33259135 DOI: 10.1002/jhbp.874
Source DB: PubMed Journal: J Hepatobiliary Pancreat Sci ISSN: 1868-6974 Impact factor: 7.027