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Current options and future possibilities for the systemic treatment of hepatocellular carcinoma

Most hepatocellular carcinoma patients could not benefit from or experience disease recurrence after curative treatments. In 2007 sorafenib demonstrated efficacy in first line treatment of advanced hepatocellular carcinoma. After a decade of negative trials, in early 2019 we now have another tyrosin...

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Autores principales: Raoul, Jean-Luc, Frenel, Jean-Sébastien, Raimbourg, Judith, Gilabert, Marine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571544/
https://www.ncbi.nlm.nih.gov/pubmed/31244990
http://dx.doi.org/10.2217/hep-2019-0001
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author Raoul, Jean-Luc
Frenel, Jean-Sébastien
Raimbourg, Judith
Gilabert, Marine
author_facet Raoul, Jean-Luc
Frenel, Jean-Sébastien
Raimbourg, Judith
Gilabert, Marine
author_sort Raoul, Jean-Luc
collection PubMed
description Most hepatocellular carcinoma patients could not benefit from or experience disease recurrence after curative treatments. In 2007 sorafenib demonstrated efficacy in first line treatment of advanced hepatocellular carcinoma. After a decade of negative trials, in early 2019 we now have another tyrosine kinase inhibitor available in first line, lenvatinib, three other targeted therapies in second line post-sorafenib (regorafenib, cabozantinib and ramucirumab) and promising data from two immunotherapies (nivolumab and pembrolizumab). Unfortunately, no biomarkers have been identified to help guide our choice. In this short review we summarize the results of these different therapies and propose a therapeutic algorithm based on subgroup analysis. It is most likely that we will not have head-to-head comparisons in second line trials.
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spelling pubmed-65715442019-06-26 Current options and future possibilities for the systemic treatment of hepatocellular carcinoma Raoul, Jean-Luc Frenel, Jean-Sébastien Raimbourg, Judith Gilabert, Marine Hepat Oncol Review Most hepatocellular carcinoma patients could not benefit from or experience disease recurrence after curative treatments. In 2007 sorafenib demonstrated efficacy in first line treatment of advanced hepatocellular carcinoma. After a decade of negative trials, in early 2019 we now have another tyrosine kinase inhibitor available in first line, lenvatinib, three other targeted therapies in second line post-sorafenib (regorafenib, cabozantinib and ramucirumab) and promising data from two immunotherapies (nivolumab and pembrolizumab). Unfortunately, no biomarkers have been identified to help guide our choice. In this short review we summarize the results of these different therapies and propose a therapeutic algorithm based on subgroup analysis. It is most likely that we will not have head-to-head comparisons in second line trials. Future Medicine Ltd 2019-06-04 /pmc/articles/PMC6571544/ /pubmed/31244990 http://dx.doi.org/10.2217/hep-2019-0001 Text en © 2019 Jean-Luc Raoul This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
Raoul, Jean-Luc
Frenel, Jean-Sébastien
Raimbourg, Judith
Gilabert, Marine
Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title_full Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title_fullStr Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title_full_unstemmed Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title_short Current options and future possibilities for the systemic treatment of hepatocellular carcinoma
title_sort current options and future possibilities for the systemic treatment of hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571544/
https://www.ncbi.nlm.nih.gov/pubmed/31244990
http://dx.doi.org/10.2217/hep-2019-0001
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