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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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 |
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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 |
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