Cargando…

Targeted therapy for hepatocellular carcinoma

The last 3 years have seen the emergence of promising targeted therapies for the treatment of hepatocellular carcinoma (HCC). Sorafenib has been the mainstay of treatment for a decade and newer modalities were ineffective and did not confer any increased therapeutic benefit until the introduction of...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Ao, Yang, Xin-Rong, Chung, Wen-Yuan, Dennison, Ashley R., Zhou, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419547/
https://www.ncbi.nlm.nih.gov/pubmed/32782275
http://dx.doi.org/10.1038/s41392-020-00264-x
_version_ 1783569906752552960
author Huang, Ao
Yang, Xin-Rong
Chung, Wen-Yuan
Dennison, Ashley R.
Zhou, Jian
author_facet Huang, Ao
Yang, Xin-Rong
Chung, Wen-Yuan
Dennison, Ashley R.
Zhou, Jian
author_sort Huang, Ao
collection PubMed
description The last 3 years have seen the emergence of promising targeted therapies for the treatment of hepatocellular carcinoma (HCC). Sorafenib has been the mainstay of treatment for a decade and newer modalities were ineffective and did not confer any increased therapeutic benefit until the introduction of lenvatinib which was approved based on its non-inferiority to sorafenib. The subsequent success of regorafenib in HCC patients who progress on sorafenib treatment heralded a new era of second-line treatment and was quickly followed by ramucirumab, cabozantinib, and the most influential, immune checkpoint inhibitors (ICIs). Over the same period combination therapies, including anti-angiogenesis agents with ICIs, dual ICIs and targeted agents in conjunction with surgery or other loco-regional therapies, have been extensively investigated and have shown promise and provided the basis for exciting clinical trials. Work continues to develop additional novel therapeutic agents which could potentially augment the presently available options and understand the underlying mechanisms responsible for drug resistance, with the goal of improving the survival of patients with HCC.
format Online
Article
Text
id pubmed-7419547
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-74195472020-08-18 Targeted therapy for hepatocellular carcinoma Huang, Ao Yang, Xin-Rong Chung, Wen-Yuan Dennison, Ashley R. Zhou, Jian Signal Transduct Target Ther Review Article The last 3 years have seen the emergence of promising targeted therapies for the treatment of hepatocellular carcinoma (HCC). Sorafenib has been the mainstay of treatment for a decade and newer modalities were ineffective and did not confer any increased therapeutic benefit until the introduction of lenvatinib which was approved based on its non-inferiority to sorafenib. The subsequent success of regorafenib in HCC patients who progress on sorafenib treatment heralded a new era of second-line treatment and was quickly followed by ramucirumab, cabozantinib, and the most influential, immune checkpoint inhibitors (ICIs). Over the same period combination therapies, including anti-angiogenesis agents with ICIs, dual ICIs and targeted agents in conjunction with surgery or other loco-regional therapies, have been extensively investigated and have shown promise and provided the basis for exciting clinical trials. Work continues to develop additional novel therapeutic agents which could potentially augment the presently available options and understand the underlying mechanisms responsible for drug resistance, with the goal of improving the survival of patients with HCC. Nature Publishing Group UK 2020-08-11 /pmc/articles/PMC7419547/ /pubmed/32782275 http://dx.doi.org/10.1038/s41392-020-00264-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Huang, Ao
Yang, Xin-Rong
Chung, Wen-Yuan
Dennison, Ashley R.
Zhou, Jian
Targeted therapy for hepatocellular carcinoma
title Targeted therapy for hepatocellular carcinoma
title_full Targeted therapy for hepatocellular carcinoma
title_fullStr Targeted therapy for hepatocellular carcinoma
title_full_unstemmed Targeted therapy for hepatocellular carcinoma
title_short Targeted therapy for hepatocellular carcinoma
title_sort targeted therapy for hepatocellular carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419547/
https://www.ncbi.nlm.nih.gov/pubmed/32782275
http://dx.doi.org/10.1038/s41392-020-00264-x
work_keys_str_mv AT huangao targetedtherapyforhepatocellularcarcinoma
AT yangxinrong targetedtherapyforhepatocellularcarcinoma
AT chungwenyuan targetedtherapyforhepatocellularcarcinoma
AT dennisonashleyr targetedtherapyforhepatocellularcarcinoma
AT zhoujian targetedtherapyforhepatocellularcarcinoma