Immune checkpoint inhibitors for hepatocellular carcinoma
The position of immunotherapy as a pillar of systemic cancer treatment has been firmly established over the past decade. Immune checkpoint inhibitors are a welcome option for patients with different malignancies. This is in part because they offer the possibility of durable benefit, even for patient...
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Veröffentlicht in: | Cancer 2019-10, Vol.125 (19), p.3312-3319 |
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description | The position of immunotherapy as a pillar of systemic cancer treatment has been firmly established over the past decade. Immune checkpoint inhibitors are a welcome option for patients with different malignancies. This is in part because they offer the possibility of durable benefit, even for patients who have failed other treatment modalities. The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma (HCC) is a milestone in the history of this recalcitrant disease. The treatment of HCC has been a challenge, and for many years was limited to the tyrosine kinase inhibitor sorafenib and to several novel tyrosine kinase inhibitors that have shown efficacy and have been approved. The current role of immune checkpoint inhibitors in the management of HCC, and how this role is likely to evolve in the years ahead, are key. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, including novel therapies are evolving. This is understandably of special interest considering the potential unique immune system of the liver, which may impact the use of immunotherapy in patients with HCC going forward, and how can it be enhanced further.
The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma is a milestone in the history of this recalcitrant disease. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, as well as with novel therapies are evolving. |
doi_str_mv | 10.1002/cncr.32076 |
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The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma is a milestone in the history of this recalcitrant disease. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, as well as with novel therapies are evolving.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.32076</identifier><identifier>PMID: 31290997</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adaptive Immunity - drug effects ; Antineoplastic Agents, Immunological - pharmacology ; Antineoplastic Agents, Immunological - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer ; Carcinoma, Hepatocellular - immunology ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Hepatocellular - therapy ; checkpoint inhibitor ; Chemoembolization, Therapeutic - methods ; Clinical Trials as Topic ; Combined Modality Therapy - methods ; CTLA-4 Antigen - antagonists & inhibitors ; CTLA-4 Antigen - immunology ; CTLA‐4 ; durvalumab ; Enzyme inhibitors ; Hepatocellular carcinoma ; Humans ; Immune checkpoint inhibitors ; Immune system ; Immunotherapy ; Inhibitors ; Kinases ; Liver - drug effects ; Liver - immunology ; Liver - pathology ; Liver cancer ; Liver Neoplasms - immunology ; Liver Neoplasms - pathology ; Liver Neoplasms - therapy ; Medical treatment ; Monoclonal antibodies ; nivolumab ; Oncology ; PD‐1 ; pembrolizumab ; Programmed Cell Death 1 Receptor - antagonists & inhibitors ; Programmed Cell Death 1 Receptor - immunology ; Protein-tyrosine kinase ; Targeted cancer therapy ; Treatment Outcome ; tremelimumab ; Tumor Escape - drug effects ; Tumor Microenvironment - drug effects ; Tumor Microenvironment - immunology ; Tyrosine</subject><ispartof>Cancer, 2019-10, Vol.125 (19), p.3312-3319</ispartof><rights>2019 American Cancer Society</rights><rights>2019 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5146-4861d574ca5da6cfa4abaa58bdadc62898eef073721e67377c8dfad84270e7483</citedby><cites>FETCH-LOGICAL-c5146-4861d574ca5da6cfa4abaa58bdadc62898eef073721e67377c8dfad84270e7483</cites><orcidid>0000-0002-1522-8054</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.32076$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.32076$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31290997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El Dika, Imane</creatorcontrib><creatorcontrib>Khalil, Danny N.</creatorcontrib><creatorcontrib>Abou‐Alfa, Ghassan K.</creatorcontrib><title>Immune checkpoint inhibitors for hepatocellular carcinoma</title><title>Cancer</title><addtitle>Cancer</addtitle><description>The position of immunotherapy as a pillar of systemic cancer treatment has been firmly established over the past decade. Immune checkpoint inhibitors are a welcome option for patients with different malignancies. This is in part because they offer the possibility of durable benefit, even for patients who have failed other treatment modalities. The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma (HCC) is a milestone in the history of this recalcitrant disease. The treatment of HCC has been a challenge, and for many years was limited to the tyrosine kinase inhibitor sorafenib and to several novel tyrosine kinase inhibitors that have shown efficacy and have been approved. The current role of immune checkpoint inhibitors in the management of HCC, and how this role is likely to evolve in the years ahead, are key. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, including novel therapies are evolving. This is understandably of special interest considering the potential unique immune system of the liver, which may impact the use of immunotherapy in patients with HCC going forward, and how can it be enhanced further.
The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma is a milestone in the history of this recalcitrant disease. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, as well as with novel therapies are evolving.</description><subject>Adaptive Immunity - drug effects</subject><subject>Antineoplastic Agents, Immunological - pharmacology</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer</subject><subject>Carcinoma, Hepatocellular - immunology</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>checkpoint inhibitor</subject><subject>Chemoembolization, Therapeutic - methods</subject><subject>Clinical Trials as Topic</subject><subject>Combined Modality Therapy - methods</subject><subject>CTLA-4 Antigen - antagonists & inhibitors</subject><subject>CTLA-4 Antigen - immunology</subject><subject>CTLA‐4</subject><subject>durvalumab</subject><subject>Enzyme inhibitors</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>Inhibitors</subject><subject>Kinases</subject><subject>Liver - drug effects</subject><subject>Liver - immunology</subject><subject>Liver - pathology</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - immunology</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver Neoplasms - therapy</subject><subject>Medical treatment</subject><subject>Monoclonal antibodies</subject><subject>nivolumab</subject><subject>Oncology</subject><subject>PD‐1</subject><subject>pembrolizumab</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>Programmed Cell Death 1 Receptor - immunology</subject><subject>Protein-tyrosine kinase</subject><subject>Targeted cancer therapy</subject><subject>Treatment Outcome</subject><subject>tremelimumab</subject><subject>Tumor Escape - drug effects</subject><subject>Tumor Microenvironment - drug effects</subject><subject>Tumor Microenvironment - immunology</subject><subject>Tyrosine</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kdFKHDEUhkNRdLt60weQAW-kMDbJJJPkRpDFtsKiUCz0LpzNZNzoTLImMy379ma7dqleeHU4nI-P__Aj9Ingc4Ix_WK8iecVxaL-gCYEK1FiwugemmCMZclZ9esQfUzpIa-C8uoAHVaEKqyUmCB13fejt4VZWvO4Cs4PhfNLt3BDiKloQyyWdgVDMLbrxg5iYSAa50MPR2i_hS7Z45c5RT-_Xt3Nvpfz22_Xs8t5aThhdclkTRoumAHeQG1aYLAA4HLRQGNqKpW0tsWiEpTYOg9hZNNCIxkV2Aomqym62HpX46K3jbF-iNDpVXQ9xLUO4PTri3dLfR9-a6EY4xRnwdmLIIan0aZB9y5t_gFvw5g0pZwzrjgmGT19gz6EMfr8Xqak4jXnlcrU5y1lYkgp2nYXhmC9aURvGtF_G8nwyf_xd-i_CjJAtsAf19n1Oyo9u5n92EqfAdazl0g</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>El Dika, Imane</creator><creator>Khalil, Danny N.</creator><creator>Abou‐Alfa, Ghassan K.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1522-8054</orcidid></search><sort><creationdate>20191001</creationdate><title>Immune checkpoint inhibitors for hepatocellular carcinoma</title><author>El Dika, Imane ; Khalil, Danny N. ; Abou‐Alfa, Ghassan K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5146-4861d574ca5da6cfa4abaa58bdadc62898eef073721e67377c8dfad84270e7483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adaptive Immunity - drug effects</topic><topic>Antineoplastic Agents, Immunological - pharmacology</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cancer</topic><topic>Carcinoma, Hepatocellular - immunology</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>checkpoint inhibitor</topic><topic>Chemoembolization, Therapeutic - methods</topic><topic>Clinical Trials as Topic</topic><topic>Combined Modality Therapy - methods</topic><topic>CTLA-4 Antigen - antagonists & inhibitors</topic><topic>CTLA-4 Antigen - immunology</topic><topic>CTLA‐4</topic><topic>durvalumab</topic><topic>Enzyme inhibitors</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>Inhibitors</topic><topic>Kinases</topic><topic>Liver - drug effects</topic><topic>Liver - immunology</topic><topic>Liver - pathology</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - immunology</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver Neoplasms - therapy</topic><topic>Medical treatment</topic><topic>Monoclonal antibodies</topic><topic>nivolumab</topic><topic>Oncology</topic><topic>PD‐1</topic><topic>pembrolizumab</topic><topic>Programmed Cell Death 1 Receptor - antagonists & inhibitors</topic><topic>Programmed Cell Death 1 Receptor - immunology</topic><topic>Protein-tyrosine kinase</topic><topic>Targeted cancer therapy</topic><topic>Treatment Outcome</topic><topic>tremelimumab</topic><topic>Tumor Escape - drug effects</topic><topic>Tumor Microenvironment - drug effects</topic><topic>Tumor Microenvironment - immunology</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El Dika, Imane</creatorcontrib><creatorcontrib>Khalil, Danny N.</creatorcontrib><creatorcontrib>Abou‐Alfa, Ghassan K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El Dika, Imane</au><au>Khalil, Danny N.</au><au>Abou‐Alfa, Ghassan K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune checkpoint inhibitors for hepatocellular carcinoma</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>125</volume><issue>19</issue><spage>3312</spage><epage>3319</epage><pages>3312-3319</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>The position of immunotherapy as a pillar of systemic cancer treatment has been firmly established over the past decade. Immune checkpoint inhibitors are a welcome option for patients with different malignancies. This is in part because they offer the possibility of durable benefit, even for patients who have failed other treatment modalities. The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma (HCC) is a milestone in the history of this recalcitrant disease. The treatment of HCC has been a challenge, and for many years was limited to the tyrosine kinase inhibitor sorafenib and to several novel tyrosine kinase inhibitors that have shown efficacy and have been approved. The current role of immune checkpoint inhibitors in the management of HCC, and how this role is likely to evolve in the years ahead, are key. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, including novel therapies are evolving. This is understandably of special interest considering the potential unique immune system of the liver, which may impact the use of immunotherapy in patients with HCC going forward, and how can it be enhanced further.
The recent demonstration that immunotherapy is effective for patients with hepatocellular carcinoma is a milestone in the history of this recalcitrant disease. Other than efforts evaluating single checkpoint inhibitors, potential combination strategies, including combinations with existing local and systemic approaches, as well as with novel therapies are evolving.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31290997</pmid><doi>10.1002/cncr.32076</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1522-8054</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptive Immunity - drug effects Antineoplastic Agents, Immunological - pharmacology Antineoplastic Agents, Immunological - therapeutic use Antineoplastic Combined Chemotherapy Protocols - pharmacology Antineoplastic Combined Chemotherapy Protocols - therapeutic use Cancer Carcinoma, Hepatocellular - immunology Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - therapy checkpoint inhibitor Chemoembolization, Therapeutic - methods Clinical Trials as Topic Combined Modality Therapy - methods CTLA-4 Antigen - antagonists & inhibitors CTLA-4 Antigen - immunology CTLA‐4 durvalumab Enzyme inhibitors Hepatocellular carcinoma Humans Immune checkpoint inhibitors Immune system Immunotherapy Inhibitors Kinases Liver - drug effects Liver - immunology Liver - pathology Liver cancer Liver Neoplasms - immunology Liver Neoplasms - pathology Liver Neoplasms - therapy Medical treatment Monoclonal antibodies nivolumab Oncology PD‐1 pembrolizumab Programmed Cell Death 1 Receptor - antagonists & inhibitors Programmed Cell Death 1 Receptor - immunology Protein-tyrosine kinase Targeted cancer therapy Treatment Outcome tremelimumab Tumor Escape - drug effects Tumor Microenvironment - drug effects Tumor Microenvironment - immunology Tyrosine |
title | Immune checkpoint inhibitors for hepatocellular carcinoma |
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