Systemic Therapy for Advanced Hepatocellular Carcinoma: Current Stand and Perspectives
Hepatocellular carcinoma often develops in the context of chronic liver disease. It is the sixth most frequently diagnosed cancer and the third most common cause of cancer-related mortality worldwide. Although the mainstay of therapy is surgical resection, most patients are not eligible because of l...
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Veröffentlicht in: | Cancers 2023-03, Vol.15 (6), p.1680 |
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description | Hepatocellular carcinoma often develops in the context of chronic liver disease. It is the sixth most frequently diagnosed cancer and the third most common cause of cancer-related mortality worldwide. Although the mainstay of therapy is surgical resection, most patients are not eligible because of liver dysfunction or tumor extent. Sorafenib was the first tyrosine kinase inhibitor that improved the overall survival of patients who failed to respond to local therapies or had advanced disease, and for many years, it was the only treatment approved for the first-line setting. However, in recent years, trials have demonstrated an improvement in survival with treatments based on immunotherapy and new targeting agents, thereby extending the treatment options. A phase III trial showed that a combination of immunotherapy and targeted therapy, including atezolizumab plus bevacizumab, improved survival in the first-line setting, and is now considered the new standard of care. Other agents and combinations are being tested, including the combination of nivolumab plus ipilimumab and tremelimumab plus durvalumab, and they reportedly have clinical benefits. The aim of this manuscript is to review the latest approved therapeutic options in first- and second-line settings for advanced HCC and discuss future perspectives. |
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It is the sixth most frequently diagnosed cancer and the third most common cause of cancer-related mortality worldwide. Although the mainstay of therapy is surgical resection, most patients are not eligible because of liver dysfunction or tumor extent. Sorafenib was the first tyrosine kinase inhibitor that improved the overall survival of patients who failed to respond to local therapies or had advanced disease, and for many years, it was the only treatment approved for the first-line setting. However, in recent years, trials have demonstrated an improvement in survival with treatments based on immunotherapy and new targeting agents, thereby extending the treatment options. A phase III trial showed that a combination of immunotherapy and targeted therapy, including atezolizumab plus bevacizumab, improved survival in the first-line setting, and is now considered the new standard of care. Other agents and combinations are being tested, including the combination of nivolumab plus ipilimumab and tremelimumab plus durvalumab, and they reportedly have clinical benefits. The aim of this manuscript is to review the latest approved therapeutic options in first- and second-line settings for advanced HCC and discuss future perspectives.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15061680</identifier><identifier>PMID: 36980566</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alcohol ; Antigens ; Bevacizumab ; Cancer ; Cancer therapies ; Care and treatment ; Cell cycle ; Clinical trials ; Disease control ; Hepatitis B ; Hepatitis C ; Hepatocellular carcinoma ; Hepatoma ; Immune system ; Immunotherapy ; Infections ; Interferon ; Kinases ; Ligands ; Liver cancer ; Liver cirrhosis ; Liver diseases ; Medical prognosis ; Mutation ; Patients ; Protein-tyrosine kinase ; Review ; Survival ; Tumors ; Vascular endothelial growth factor ; Viral infections</subject><ispartof>Cancers, 2023-03, Vol.15 (6), p.1680</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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 (https://creativecommons.org/licenses/by/4.0/). 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It is the sixth most frequently diagnosed cancer and the third most common cause of cancer-related mortality worldwide. Although the mainstay of therapy is surgical resection, most patients are not eligible because of liver dysfunction or tumor extent. Sorafenib was the first tyrosine kinase inhibitor that improved the overall survival of patients who failed to respond to local therapies or had advanced disease, and for many years, it was the only treatment approved for the first-line setting. However, in recent years, trials have demonstrated an improvement in survival with treatments based on immunotherapy and new targeting agents, thereby extending the treatment options. A phase III trial showed that a combination of immunotherapy and targeted therapy, including atezolizumab plus bevacizumab, improved survival in the first-line setting, and is now considered the new standard of care. Other agents and combinations are being tested, including the combination of nivolumab plus ipilimumab and tremelimumab plus durvalumab, and they reportedly have clinical benefits. The aim of this manuscript is to review the latest approved therapeutic options in first- and second-line settings for advanced HCC and discuss future perspectives.</description><subject>Alcohol</subject><subject>Antigens</subject><subject>Bevacizumab</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Cell cycle</subject><subject>Clinical trials</subject><subject>Disease control</subject><subject>Hepatitis B</subject><subject>Hepatitis C</subject><subject>Hepatocellular carcinoma</subject><subject>Hepatoma</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>Infections</subject><subject>Interferon</subject><subject>Kinases</subject><subject>Ligands</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver diseases</subject><subject>Medical prognosis</subject><subject>Mutation</subject><subject>Patients</subject><subject>Protein-tyrosine kinase</subject><subject>Review</subject><subject>Survival</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><subject>Viral infections</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptks9rFTEQx4MottSevcmCFy-vze9svMjjoVYoKLR6DXnJbJuym6zJ7oP335ulv4sJIUPymW9mMoPQe4JPGNP41NnoIBcisCSyxa_QIcWKrqTU_PUT-wAdl3KD62CMKKneogMmdYuFlIfoz8W-TDAE11xeQ7bjvulSbtZ-t2j75gxGOyUHfT_3Njcbm12IabCfm82cM8SpuZhs9M2yftVYRnBT2EF5h950ti9wfLcfod_fvl5uzlbnP7__2KzPV463eloxobx2W7H1XFlMOWk9KCukp9ITTp0TnSCEUtq2wjGlVWe3HqBaALrjkh2hL7e647wdwLsaUba9GXMYbN6bZIN5fhPDtblKO0Mw5lIoXBU-3Snk9HeGMpkhlCVhGyHNxVClqcCaUFbRjy_QmzTnWPNbKCK05lg9Ule2BxNil-rDbhE1a8WZkoQKUamT_1B1-qUYKUIX6vkzh9NbB5dTKRm6hyQJNks7mBftUD0-PP2bB_6--OwfHhuw7g</recordid><startdate>20230309</startdate><enddate>20230309</enddate><creator>Girardi, Daniel M</creator><creator>Sousa, Lara P</creator><creator>Miranda, Thiago A</creator><creator>Haum, Fernanda N C</creator><creator>Pereira, Gabriel C B</creator><creator>Pereira, Allan A L</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4984-746X</orcidid><orcidid>https://orcid.org/0000-0002-8573-7364</orcidid></search><sort><creationdate>20230309</creationdate><title>Systemic Therapy for Advanced Hepatocellular Carcinoma: Current Stand and Perspectives</title><author>Girardi, Daniel M ; Sousa, Lara P ; Miranda, Thiago A ; Haum, Fernanda N C ; Pereira, Gabriel C B ; Pereira, Allan A L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-357d9cb5bd47a02418de7a56d26d142cc5f511222885c3797fabdee379ee9f463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alcohol</topic><topic>Antigens</topic><topic>Bevacizumab</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Cell cycle</topic><topic>Clinical trials</topic><topic>Disease control</topic><topic>Hepatitis B</topic><topic>Hepatitis C</topic><topic>Hepatocellular carcinoma</topic><topic>Hepatoma</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>Infections</topic><topic>Interferon</topic><topic>Kinases</topic><topic>Ligands</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver diseases</topic><topic>Medical prognosis</topic><topic>Mutation</topic><topic>Patients</topic><topic>Protein-tyrosine kinase</topic><topic>Review</topic><topic>Survival</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Girardi, Daniel M</creatorcontrib><creatorcontrib>Sousa, Lara P</creatorcontrib><creatorcontrib>Miranda, Thiago A</creatorcontrib><creatorcontrib>Haum, Fernanda N C</creatorcontrib><creatorcontrib>Pereira, Gabriel C B</creatorcontrib><creatorcontrib>Pereira, Allan A L</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Girardi, Daniel M</au><au>Sousa, Lara P</au><au>Miranda, Thiago A</au><au>Haum, Fernanda N C</au><au>Pereira, Gabriel C B</au><au>Pereira, Allan A L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systemic Therapy for Advanced Hepatocellular Carcinoma: Current Stand and Perspectives</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-03-09</date><risdate>2023</risdate><volume>15</volume><issue>6</issue><spage>1680</spage><pages>1680-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Hepatocellular carcinoma often develops in the context of chronic liver disease. It is the sixth most frequently diagnosed cancer and the third most common cause of cancer-related mortality worldwide. Although the mainstay of therapy is surgical resection, most patients are not eligible because of liver dysfunction or tumor extent. Sorafenib was the first tyrosine kinase inhibitor that improved the overall survival of patients who failed to respond to local therapies or had advanced disease, and for many years, it was the only treatment approved for the first-line setting. However, in recent years, trials have demonstrated an improvement in survival with treatments based on immunotherapy and new targeting agents, thereby extending the treatment options. A phase III trial showed that a combination of immunotherapy and targeted therapy, including atezolizumab plus bevacizumab, improved survival in the first-line setting, and is now considered the new standard of care. Other agents and combinations are being tested, including the combination of nivolumab plus ipilimumab and tremelimumab plus durvalumab, and they reportedly have clinical benefits. The aim of this manuscript is to review the latest approved therapeutic options in first- and second-line settings for advanced HCC and discuss future perspectives.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36980566</pmid><doi>10.3390/cancers15061680</doi><orcidid>https://orcid.org/0000-0002-4984-746X</orcidid><orcidid>https://orcid.org/0000-0002-8573-7364</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Antigens Bevacizumab Cancer Cancer therapies Care and treatment Cell cycle Clinical trials Disease control Hepatitis B Hepatitis C Hepatocellular carcinoma Hepatoma Immune system Immunotherapy Infections Interferon Kinases Ligands Liver cancer Liver cirrhosis Liver diseases Medical prognosis Mutation Patients Protein-tyrosine kinase Review Survival Tumors Vascular endothelial growth factor Viral infections |
title | Systemic Therapy for Advanced Hepatocellular Carcinoma: Current Stand and Perspectives |
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