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Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is a major cause of death among patients with liver cirrhosis. The rise of immuno‐oncology has revolutionized treatment for advanced HCC. However, most pivotal randomized controlled trials have excluded patients with moderate liver dysfunction (Child–Pugh–Turcotte B),...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358256/ https://www.ncbi.nlm.nih.gov/pubmed/37162288 http://dx.doi.org/10.1002/cam4.6033 |
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author | Costa, Frederico Wiedenmann, Bertram Roderburg, Christoph Mohr, Raphael Abou‐Alfa, Ghassan K. |
author_facet | Costa, Frederico Wiedenmann, Bertram Roderburg, Christoph Mohr, Raphael Abou‐Alfa, Ghassan K. |
author_sort | Costa, Frederico |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is a major cause of death among patients with liver cirrhosis. The rise of immuno‐oncology has revolutionized treatment for advanced HCC. However, most pivotal randomized controlled trials have excluded patients with moderate liver dysfunction (Child–Pugh–Turcotte B), despite the high incidence of liver disease in patients with HCC at the time of diagnosis. Overall survival in patients with HCC and moderate liver dysfunction treated with sorafenib has been found to be only approximately 3–5 months, underlining the need for improved treatment algorithms for this increasingly important subgroup of patients. In this review, we summarize available data on the treatment of patients with HCC and moderate liver dysfunction. Opportunities, as well as clinical challenges, are discussed in detail, highlighting potential changes to the therapeutic landscape. |
format | Online Article Text |
id | pubmed-10358256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103582562023-07-21 Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma Costa, Frederico Wiedenmann, Bertram Roderburg, Christoph Mohr, Raphael Abou‐Alfa, Ghassan K. Cancer Med REVIEWS Hepatocellular carcinoma (HCC) is a major cause of death among patients with liver cirrhosis. The rise of immuno‐oncology has revolutionized treatment for advanced HCC. However, most pivotal randomized controlled trials have excluded patients with moderate liver dysfunction (Child–Pugh–Turcotte B), despite the high incidence of liver disease in patients with HCC at the time of diagnosis. Overall survival in patients with HCC and moderate liver dysfunction treated with sorafenib has been found to be only approximately 3–5 months, underlining the need for improved treatment algorithms for this increasingly important subgroup of patients. In this review, we summarize available data on the treatment of patients with HCC and moderate liver dysfunction. Opportunities, as well as clinical challenges, are discussed in detail, highlighting potential changes to the therapeutic landscape. John Wiley and Sons Inc. 2023-05-10 /pmc/articles/PMC10358256/ /pubmed/37162288 http://dx.doi.org/10.1002/cam4.6033 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | REVIEWS Costa, Frederico Wiedenmann, Bertram Roderburg, Christoph Mohr, Raphael Abou‐Alfa, Ghassan K. Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title | Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title_full | Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title_fullStr | Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title_full_unstemmed | Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title_short | Systemic treatment in patients with Child–Pugh B liver dysfunction and advanced hepatocellular carcinoma |
title_sort | systemic treatment in patients with child–pugh b liver dysfunction and advanced hepatocellular carcinoma |
topic | REVIEWS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358256/ https://www.ncbi.nlm.nih.gov/pubmed/37162288 http://dx.doi.org/10.1002/cam4.6033 |
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