Immunotherapy of Lymphoma and Myeloma: Facts and Hopes
Immune checkpoint blockade has driven a revolution in modern oncology, and robust drug development of immune checkpoint inhibitors is underway in both solid tumors and hematologic malignancies. High response rates to programmed cell death 1 (PD-1) blockade using nivolumab or pembrolizumab in classic...
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Veröffentlicht in: | Clinical cancer research 2018-03, Vol.24 (5), p.1002-1010 |
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description | Immune checkpoint blockade has driven a revolution in modern oncology, and robust drug development of immune checkpoint inhibitors is underway in both solid tumors and hematologic malignancies. High response rates to programmed cell death 1 (PD-1) blockade using nivolumab or pembrolizumab in classical Hodgkin lymphoma (cHL) and several variants of non-Hodgkin lymphoma (NHL) revealed an intrinsic biological sensitivity to this approach, and work is ongoing exploring combinations with immune checkpoint inhibitors in both cHL and NHL. There are also preliminary data suggesting antitumor efficacy of PD-1 inhibitors used in combination with immunomodulatory drugs in multiple myeloma, and effects of novel monoclonal antibody therapies on the tumor microenvironment may lead to synergy with checkpoint blockade. Although immune checkpoint inhibitors are generally well tolerated, clinicians must use caution and remain vigilant when treating patients with these agents in order to identify immune-related toxicities and prevent treatment-related morbidity and mortality. Autologous stem cell transplant is a useful tool for treatment of hematologic malignancies and has potential as a platform for use of immune checkpoint inhibitors. An important safety signal has emerged surrounding the risk of graft-versus-host disease associated with use of PD-1 inhibitors before and after allogeneic stem cell transplant. We aim to discuss the facts known to date in the use of immune checkpoint inhibitors for patients with lymphoid malignancies and our hopes for expanding the benefits of immunotherapy to patients in the future.
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.</description><subject>Anticancer properties</subject><subject>Antineoplastic Agents, Immunological - pharmacology</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Autografts</subject><subject>Cancer</subject><subject>Cell death</subject><subject>Chemoradiotherapy - methods</subject><subject>Chemoradiotherapy - trends</subject><subject>Drug development</subject><subject>Graft-versus-host reaction</subject><subject>Health risks</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Hematopoietic Stem Cell Transplantation - trends</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunomodulation</subject><subject>Immunosuppressive agents</subject><subject>Immunotherapy</subject><subject>Immunotherapy - methods</subject><subject>Immunotherapy - trends</subject><subject>Inhibitors</subject><subject>Lymphoma</subject><subject>Lymphoma - immunology</subject><subject>Lymphoma - therapy</subject><subject>Monoclonal antibodies</subject><subject>Morbidity</subject><subject>Multiple myeloma</subject><subject>Multiple Myeloma - immunology</subject><subject>Multiple Myeloma - therapy</subject><subject>Patients</subject><subject>PD-1 protein</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>Programmed Cell Death 1 Receptor - immunology</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Solid tumors</subject><subject>Stem cells</subject><subject>Targeted cancer therapy</subject><subject>Toxicity</subject><subject>Transplantation, Autologous - methods</subject><subject>Transplantation, Autologous - trends</subject><subject>Treatment Outcome</subject><subject>Tumor Microenvironment - drug effects</subject><subject>Tumor Microenvironment - immunology</subject><subject>Tumor Microenvironment - radiation effects</subject><subject>Tumors</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEtLw0AQgBdRbK3-BCXgxUvq7DMbbxKsLVQE0fOy2e7SlrzMJof8eze29SAMzDB88-BD6BbDHGMuHzEkMgZGyTzLPmKcxMBpeoammPMkpkTw81CfmAm68n4PgBkGdokmRMo0TRMyRWJVln1Vd1vb6maIaheth7LZ1qWOdLWJ3gZbhPopWmjT-d_Wsm6sv0YXThfe3hzzDH0tXj6zZbx-f11lz-vYMA5dnDjuwk3NjTEb40QqQAITgoIhluVMOiNyDdRpTgTTJg9hUmyc0ZKCtHSGHg57m7b-7q3vVLnzxhaFrmzde4VTKgUIIDyg9__Qfd23VfhOEcCYSkxABoofKNPW3rfWqabdlbodFAY1ilWjNDVKU0GswokaxYa5u-P2Pi_t5m_qZJL-AKX8cow</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Pianko, Matthew J</creator><creator>Moskowitz, Alison J</creator><creator>Lesokhin, Alexander M</creator><general>American Association for Cancer Research 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>7QO</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20180301</creationdate><title>Immunotherapy of Lymphoma and Myeloma: Facts and Hopes</title><author>Pianko, Matthew J ; Moskowitz, Alison J ; Lesokhin, Alexander M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-7f5f141a5cccdcf69608046630c2e4b48fc6ba03fa5264acbacbc91cfca8308e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer properties</topic><topic>Antineoplastic Agents, Immunological - pharmacology</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Autografts</topic><topic>Cancer</topic><topic>Cell death</topic><topic>Chemoradiotherapy - methods</topic><topic>Chemoradiotherapy - trends</topic><topic>Drug development</topic><topic>Graft-versus-host reaction</topic><topic>Health risks</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Hematopoietic Stem Cell Transplantation - trends</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immunomodulation</topic><topic>Immunosuppressive agents</topic><topic>Immunotherapy</topic><topic>Immunotherapy - methods</topic><topic>Immunotherapy - trends</topic><topic>Inhibitors</topic><topic>Lymphoma</topic><topic>Lymphoma - immunology</topic><topic>Lymphoma - therapy</topic><topic>Monoclonal antibodies</topic><topic>Morbidity</topic><topic>Multiple myeloma</topic><topic>Multiple Myeloma - immunology</topic><topic>Multiple Myeloma - therapy</topic><topic>Patients</topic><topic>PD-1 protein</topic><topic>Programmed Cell Death 1 Receptor - antagonists & inhibitors</topic><topic>Programmed Cell Death 1 Receptor - immunology</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Solid tumors</topic><topic>Stem cells</topic><topic>Targeted cancer therapy</topic><topic>Toxicity</topic><topic>Transplantation, Autologous - methods</topic><topic>Transplantation, Autologous - trends</topic><topic>Treatment Outcome</topic><topic>Tumor Microenvironment - drug effects</topic><topic>Tumor Microenvironment - immunology</topic><topic>Tumor Microenvironment - radiation effects</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pianko, Matthew J</creatorcontrib><creatorcontrib>Moskowitz, Alison J</creatorcontrib><creatorcontrib>Lesokhin, Alexander M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pianko, Matthew J</au><au>Moskowitz, Alison J</au><au>Lesokhin, Alexander M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotherapy of Lymphoma and Myeloma: Facts and Hopes</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2018-03-01</date><risdate>2018</risdate><volume>24</volume><issue>5</issue><spage>1002</spage><epage>1010</epage><pages>1002-1010</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Immune checkpoint blockade has driven a revolution in modern oncology, and robust drug development of immune checkpoint inhibitors is underway in both solid tumors and hematologic malignancies. High response rates to programmed cell death 1 (PD-1) blockade using nivolumab or pembrolizumab in classical Hodgkin lymphoma (cHL) and several variants of non-Hodgkin lymphoma (NHL) revealed an intrinsic biological sensitivity to this approach, and work is ongoing exploring combinations with immune checkpoint inhibitors in both cHL and NHL. There are also preliminary data suggesting antitumor efficacy of PD-1 inhibitors used in combination with immunomodulatory drugs in multiple myeloma, and effects of novel monoclonal antibody therapies on the tumor microenvironment may lead to synergy with checkpoint blockade. Although immune checkpoint inhibitors are generally well tolerated, clinicians must use caution and remain vigilant when treating patients with these agents in order to identify immune-related toxicities and prevent treatment-related morbidity and mortality. Autologous stem cell transplant is a useful tool for treatment of hematologic malignancies and has potential as a platform for use of immune checkpoint inhibitors. An important safety signal has emerged surrounding the risk of graft-versus-host disease associated with use of PD-1 inhibitors before and after allogeneic stem cell transplant. We aim to discuss the facts known to date in the use of immune checkpoint inhibitors for patients with lymphoid malignancies and our hopes for expanding the benefits of immunotherapy to patients in the future.
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subjects | Anticancer properties Antineoplastic Agents, Immunological - pharmacology Antineoplastic Agents, Immunological - therapeutic use Antitumor activity Apoptosis Autografts Cancer Cell death Chemoradiotherapy - methods Chemoradiotherapy - trends Drug development Graft-versus-host reaction Health risks Hematopoietic Stem Cell Transplantation - methods Hematopoietic Stem Cell Transplantation - trends Humans Immune checkpoint inhibitors Immunomodulation Immunosuppressive agents Immunotherapy Immunotherapy - methods Immunotherapy - trends Inhibitors Lymphoma Lymphoma - immunology Lymphoma - therapy Monoclonal antibodies Morbidity Multiple myeloma Multiple Myeloma - immunology Multiple Myeloma - therapy Patients PD-1 protein Programmed Cell Death 1 Receptor - antagonists & inhibitors Programmed Cell Death 1 Receptor - immunology Randomized Controlled Trials as Topic Solid tumors Stem cells Targeted cancer therapy Toxicity Transplantation, Autologous - methods Transplantation, Autologous - trends Treatment Outcome Tumor Microenvironment - drug effects Tumor Microenvironment - immunology Tumor Microenvironment - radiation effects Tumors |
title | Immunotherapy of Lymphoma and Myeloma: Facts and Hopes |
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