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Tumor immune response and immunotherapy in gastric cancer
Remarkable developments in immuno-oncology have changed the landscape of gastric cancer (GC) treatment. Because immunotherapy intervenes with tumor immune response rather than directly targeting tumor cells, it is important to develop a greater understanding of tumor immunity. This review paper summ...
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Published in: | Journal of pathology and translational medicine 2020, 54(1), , pp.20-33 |
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description | Remarkable developments in immuno-oncology have changed the landscape of gastric cancer (GC) treatment. Because immunotherapy intervenes with tumor immune response rather than directly targeting tumor cells, it is important to develop a greater understanding of tumor immunity. This review paper summarizes the tumor immune reaction and immune escape mechanisms while focusing on the role of T cells and their co-inhibitory signals, such as the immune checkpoint molecules programmed death-1 and programmed deathligand 1 (PD-L1). This paper also describes past clinical trials of immunotherapy for patients with GC and details their clinical implications. Strong predictive markers are essential to improve response to immunotherapy. Microsatellite instability, Epstein-Barr virus, PD-L1 expression, and tumor mutational burden are now regarded as potent predictive markers for immunotherapy in patients with GC. Novel immunotherapy and combination therapy targeting new immune checkpoint molecules such as lymphocyte-activation gene 3, T cell immunoglobulin, and mucin domain containing-3, and indoleamine 2,3-dioxygenase have been suggested, and trials are ongoing to evaluate their safety and efficacy. Immunotherapy is an important treatment option for patients with GC and has great potential for improving patient outcome, and further research in immuno-oncology should be carried out. |
doi_str_mv | 10.4132/jptm.2019.10.08 |
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Because immunotherapy intervenes with tumor immune response rather than directly targeting tumor cells, it is important to develop a greater understanding of tumor immunity. This review paper summarizes the tumor immune reaction and immune escape mechanisms while focusing on the role of T cells and their co-inhibitory signals, such as the immune checkpoint molecules programmed death-1 and programmed deathligand 1 (PD-L1). This paper also describes past clinical trials of immunotherapy for patients with GC and details their clinical implications. Strong predictive markers are essential to improve response to immunotherapy. Microsatellite instability, Epstein-Barr virus, PD-L1 expression, and tumor mutational burden are now regarded as potent predictive markers for immunotherapy in patients with GC. Novel immunotherapy and combination therapy targeting new immune checkpoint molecules such as lymphocyte-activation gene 3, T cell immunoglobulin, and mucin domain containing-3, and indoleamine 2,3-dioxygenase have been suggested, and trials are ongoing to evaluate their safety and efficacy. Immunotherapy is an important treatment option for patients with GC and has great potential for improving patient outcome, and further research in immuno-oncology should be carried out.</description><identifier>ISSN: 2383-7837</identifier><identifier>EISSN: 2383-7845</identifier><identifier>DOI: 10.4132/jptm.2019.10.08</identifier><identifier>PMID: 31674166</identifier><language>eng</language><publisher>Korea (South): Korean Society of Pathologists, Korean Society for Cytopathology</publisher><subject>Antigens ; Apoptosis ; biomarker ; Biomarkers ; Cell adhesion & migration ; Cell division ; Cell growth ; Clinical trials ; Cytotoxicity ; epstein-barr virus ; Gastric cancer ; Genes ; Growth factors ; Immune system ; Immunoglobulins ; Immunotherapy ; Ligands ; Lymphocytes ; microsatellite instability ; Mutation ; Oncology ; Patients ; programmed cell death-ligand 1 ; Proteins ; Review ; stomach neoplasms ; T cell receptors ; tumor mutational burden ; tumor-infiltrating lymphocytes ; Tumors ; Viruses ; 병리학</subject><ispartof>Journal of Pathology and Translational Medicine, 2020, 54(1), , pp.20-33</ispartof><rights>2020. 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Because immunotherapy intervenes with tumor immune response rather than directly targeting tumor cells, it is important to develop a greater understanding of tumor immunity. This review paper summarizes the tumor immune reaction and immune escape mechanisms while focusing on the role of T cells and their co-inhibitory signals, such as the immune checkpoint molecules programmed death-1 and programmed deathligand 1 (PD-L1). This paper also describes past clinical trials of immunotherapy for patients with GC and details their clinical implications. Strong predictive markers are essential to improve response to immunotherapy. Microsatellite instability, Epstein-Barr virus, PD-L1 expression, and tumor mutational burden are now regarded as potent predictive markers for immunotherapy in patients with GC. Novel immunotherapy and combination therapy targeting new immune checkpoint molecules such as lymphocyte-activation gene 3, T cell immunoglobulin, and mucin domain containing-3, and indoleamine 2,3-dioxygenase have been suggested, and trials are ongoing to evaluate their safety and efficacy. Immunotherapy is an important treatment option for patients with GC and has great potential for improving patient outcome, and further research in immuno-oncology should be carried out.</description><subject>Antigens</subject><subject>Apoptosis</subject><subject>biomarker</subject><subject>Biomarkers</subject><subject>Cell adhesion & migration</subject><subject>Cell division</subject><subject>Cell growth</subject><subject>Clinical trials</subject><subject>Cytotoxicity</subject><subject>epstein-barr virus</subject><subject>Gastric cancer</subject><subject>Genes</subject><subject>Growth factors</subject><subject>Immune system</subject><subject>Immunoglobulins</subject><subject>Immunotherapy</subject><subject>Ligands</subject><subject>Lymphocytes</subject><subject>microsatellite instability</subject><subject>Mutation</subject><subject>Oncology</subject><subject>Patients</subject><subject>programmed cell death-ligand 1</subject><subject>Proteins</subject><subject>Review</subject><subject>stomach neoplasms</subject><subject>T cell receptors</subject><subject>tumor mutational burden</subject><subject>tumor-infiltrating lymphocytes</subject><subject>Tumors</subject><subject>Viruses</subject><subject>병리학</subject><issn>2383-7837</issn><issn>2383-7845</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks1r3DAQxUVpaUKac2_F0Etz2I1kSWPpUgghSRcChWTvQtbHxhtbciW7kP--9jpdmp5GPP3maSQ9hD4TvGaElpf7fujWJSZyPSlYvEOnJRV0VQnG3x_XtDpB5znvMcaEcQpMfkQnlEDFCMApktuxi6loum4Mrkgu9zFkV-hgFy0OTy7p_qVoQrHTeUiNKYwOxqVP6IPXbXbnr_UMPd7ebK9_rO5_3m2ur-5XhpdkWAHnjDBnsOBGUMErryUvrWcOBCVGGiDgagt1LaTFAFY6wRhm3nEqPD1DF4trSF49m0ZF3RzqLqrnpK4ethsFXJZYyIndLKyNeq_61HQ6vRwaDkJMO6XT0JjWKQElw9bXnFnMwMga6tJj76W11Fs-n_t98erHunPWuDAk3b4xfbsTmqdppt8KpABZscng26tBir9GlwfVNdm4ttXBxTGrkhICvBLAJ_Trf-g-jilMjzpRQmAsSTVTlwtlUsw5OX8chmA150HNeVBzHmYFi6njy793OPJ_f5_-ASWosLM</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Kwak, Yoonjin</creator><creator>Seo, An Na</creator><creator>Lee, Hee Eun</creator><creator>Lee, Hye Seung</creator><general>Korean Society of Pathologists, Korean Society for Cytopathology</general><general>The Korean Society of Pathologists and the Korean Society for Cytopathology</general><general>Korean Society of Pathologists & the Korean Society for Cytopathology</general><general>대한병리학회</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BVBZV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope></search><sort><creationdate>20200101</creationdate><title>Tumor immune response and immunotherapy in gastric cancer</title><author>Kwak, Yoonjin ; Seo, An Na ; Lee, Hee Eun ; Lee, Hye Seung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-655414ec085c83857fa952df4e6831c9c616ebd6bb89d066d9e84404fe538f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antigens</topic><topic>Apoptosis</topic><topic>biomarker</topic><topic>Biomarkers</topic><topic>Cell adhesion & migration</topic><topic>Cell division</topic><topic>Cell growth</topic><topic>Clinical trials</topic><topic>Cytotoxicity</topic><topic>epstein-barr virus</topic><topic>Gastric cancer</topic><topic>Genes</topic><topic>Growth factors</topic><topic>Immune system</topic><topic>Immunoglobulins</topic><topic>Immunotherapy</topic><topic>Ligands</topic><topic>Lymphocytes</topic><topic>microsatellite instability</topic><topic>Mutation</topic><topic>Oncology</topic><topic>Patients</topic><topic>programmed cell death-ligand 1</topic><topic>Proteins</topic><topic>Review</topic><topic>stomach neoplasms</topic><topic>T cell receptors</topic><topic>tumor mutational burden</topic><topic>tumor-infiltrating lymphocytes</topic><topic>Tumors</topic><topic>Viruses</topic><topic>병리학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kwak, Yoonjin</creatorcontrib><creatorcontrib>Seo, An Na</creatorcontrib><creatorcontrib>Lee, Hee Eun</creatorcontrib><creatorcontrib>Lee, Hye Seung</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>East & South Asia Database</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><collection>Korean Citation Index</collection><jtitle>Journal of pathology and translational medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kwak, Yoonjin</au><au>Seo, An Na</au><au>Lee, Hee Eun</au><au>Lee, Hye Seung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor immune response and immunotherapy in gastric cancer</atitle><jtitle>Journal of pathology and translational medicine</jtitle><addtitle>J Pathol Transl Med</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>54</volume><issue>1</issue><spage>20</spage><epage>33</epage><pages>20-33</pages><issn>2383-7837</issn><eissn>2383-7845</eissn><abstract>Remarkable developments in immuno-oncology have changed the landscape of gastric cancer (GC) treatment. 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subjects | Antigens Apoptosis biomarker Biomarkers Cell adhesion & migration Cell division Cell growth Clinical trials Cytotoxicity epstein-barr virus Gastric cancer Genes Growth factors Immune system Immunoglobulins Immunotherapy Ligands Lymphocytes microsatellite instability Mutation Oncology Patients programmed cell death-ligand 1 Proteins Review stomach neoplasms T cell receptors tumor mutational burden tumor-infiltrating lymphocytes Tumors Viruses 병리학 |
title | Tumor immune response and immunotherapy in gastric cancer |
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