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Immune Therapy for Liver Cancers

Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) display a poor prognosis with 5-year overall survival rates around 15%, all stages taken together. These primary liver malignancies are often diagnosed at advanced stages where therapeutic options are limited. Recently, immune therapy ha...

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Detalles Bibliográficos
Autores principales: Hilmi, Marc, Vienot, Angélique, Rousseau, Benoît, Neuzillet, Cindy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016834/
https://www.ncbi.nlm.nih.gov/pubmed/31892230
http://dx.doi.org/10.3390/cancers12010077
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author Hilmi, Marc
Vienot, Angélique
Rousseau, Benoît
Neuzillet, Cindy
author_facet Hilmi, Marc
Vienot, Angélique
Rousseau, Benoît
Neuzillet, Cindy
author_sort Hilmi, Marc
collection PubMed
description Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) display a poor prognosis with 5-year overall survival rates around 15%, all stages taken together. These primary liver malignancies are often diagnosed at advanced stages where therapeutic options are limited. Recently, immune therapy has opened new opportunities in oncology. Based on their high programmed death-ligand 1 expression and tumor-infiltrating lymphocytes, HCC and BTC are theoretically good candidates for immune checkpoint blockade. However, clinical activity of single agent immunotherapy appears limited to a subset of patients, which is still ill-defined, and combinations are under investigation. In this review, we provide an overview of (i) the biological rationale for immunotherapies in HCC and BTC, (ii) the current state of their clinical development, and (iii) the predictive value of immune signatures for both clinical outcome and response to these therapies.
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spelling pubmed-70168342020-02-28 Immune Therapy for Liver Cancers Hilmi, Marc Vienot, Angélique Rousseau, Benoît Neuzillet, Cindy Cancers (Basel) Review Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) display a poor prognosis with 5-year overall survival rates around 15%, all stages taken together. These primary liver malignancies are often diagnosed at advanced stages where therapeutic options are limited. Recently, immune therapy has opened new opportunities in oncology. Based on their high programmed death-ligand 1 expression and tumor-infiltrating lymphocytes, HCC and BTC are theoretically good candidates for immune checkpoint blockade. However, clinical activity of single agent immunotherapy appears limited to a subset of patients, which is still ill-defined, and combinations are under investigation. In this review, we provide an overview of (i) the biological rationale for immunotherapies in HCC and BTC, (ii) the current state of their clinical development, and (iii) the predictive value of immune signatures for both clinical outcome and response to these therapies. MDPI 2019-12-27 /pmc/articles/PMC7016834/ /pubmed/31892230 http://dx.doi.org/10.3390/cancers12010077 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hilmi, Marc
Vienot, Angélique
Rousseau, Benoît
Neuzillet, Cindy
Immune Therapy for Liver Cancers
title Immune Therapy for Liver Cancers
title_full Immune Therapy for Liver Cancers
title_fullStr Immune Therapy for Liver Cancers
title_full_unstemmed Immune Therapy for Liver Cancers
title_short Immune Therapy for Liver Cancers
title_sort immune therapy for liver cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016834/
https://www.ncbi.nlm.nih.gov/pubmed/31892230
http://dx.doi.org/10.3390/cancers12010077
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