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Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is the third most frequent source of deaths associated with cancer after lung cancer in the world despite recent innovative treatment techniques. Liver transplantation, hepatic resection, and percutaneous ablation techniques hold great promise as potentially curative t...

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Autores principales: Eresen, Aydin, Zhang, Zhuoli, Yaghmai, Vahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743717/
https://www.ncbi.nlm.nih.gov/pubmed/35071439
http://dx.doi.org/10.21037/atm-21-3768
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author Eresen, Aydin
Zhang, Zhuoli
Yaghmai, Vahid
author_facet Eresen, Aydin
Zhang, Zhuoli
Yaghmai, Vahid
author_sort Eresen, Aydin
collection PubMed
description Hepatocellular carcinoma (HCC) is the third most frequent source of deaths associated with cancer after lung cancer in the world despite recent innovative treatment techniques. Liver transplantation, hepatic resection, and percutaneous ablation techniques hold great promise as potentially curative treatments for patients at early stages. Nevertheless, most of the patients are not suitable for these curative treatments due to their advanced disease stages at the time of diagnosis. Food and Drug Administration (FDA) approved tyrosine kinase inhibitor, sorafenib is a standard therapy for advanced-stage HCC patients which extends overall survival for several months. However, its therapeutic efficacy is restricted by adverse events and drug resistance which limits the number of patients benefiting from this systemic chemotherapeutic drug. During the last decade, novel approaches including but not limited to immunotherapies, ablation methods, and chemotherapeutic drugs were proposed to enhance sensitivity to sorafenib, improve therapeutic efficacy, and prohibit adverse events through novel delivery routes, utilization of nanoparticle carriers, and combination with other therapeutic agents. However, studies are still being conducted to optimize the efficiency of sorafenib and reduce its adverse events. In this review paper, we examine research studies evaluating novel delivery methods to reduce drug-related cytotoxicity to improve patient tolerance to sorafenib and its therapeutic efficacy in patients with HCC. Moreover, therapeutic approaches with the synergistic potential to combine with sorafenib are briefly summarized.
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spelling pubmed-87437172022-01-21 Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma Eresen, Aydin Zhang, Zhuoli Yaghmai, Vahid Ann Transl Med Review Article Hepatocellular carcinoma (HCC) is the third most frequent source of deaths associated with cancer after lung cancer in the world despite recent innovative treatment techniques. Liver transplantation, hepatic resection, and percutaneous ablation techniques hold great promise as potentially curative treatments for patients at early stages. Nevertheless, most of the patients are not suitable for these curative treatments due to their advanced disease stages at the time of diagnosis. Food and Drug Administration (FDA) approved tyrosine kinase inhibitor, sorafenib is a standard therapy for advanced-stage HCC patients which extends overall survival for several months. However, its therapeutic efficacy is restricted by adverse events and drug resistance which limits the number of patients benefiting from this systemic chemotherapeutic drug. During the last decade, novel approaches including but not limited to immunotherapies, ablation methods, and chemotherapeutic drugs were proposed to enhance sensitivity to sorafenib, improve therapeutic efficacy, and prohibit adverse events through novel delivery routes, utilization of nanoparticle carriers, and combination with other therapeutic agents. However, studies are still being conducted to optimize the efficiency of sorafenib and reduce its adverse events. In this review paper, we examine research studies evaluating novel delivery methods to reduce drug-related cytotoxicity to improve patient tolerance to sorafenib and its therapeutic efficacy in patients with HCC. Moreover, therapeutic approaches with the synergistic potential to combine with sorafenib are briefly summarized. AME Publishing Company 2021-12 /pmc/articles/PMC8743717/ /pubmed/35071439 http://dx.doi.org/10.21037/atm-21-3768 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Article
Eresen, Aydin
Zhang, Zhuoli
Yaghmai, Vahid
Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title_full Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title_fullStr Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title_full_unstemmed Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title_short Strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
title_sort strategies to improve sorafenib efficacy during image-guided treatment of hepatocellular carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743717/
https://www.ncbi.nlm.nih.gov/pubmed/35071439
http://dx.doi.org/10.21037/atm-21-3768
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