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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical cancer research 2018-03, Vol.24 (5), p.1002-1010
Hauptverfasser: Pianko, Matthew J, Moskowitz, Alison J, Lesokhin, Alexander M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1010
container_issue 5
container_start_page 1002
container_title Clinical cancer research
container_volume 24
creator Pianko, Matthew J
Moskowitz, Alison J
Lesokhin, Alexander M
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. .
doi_str_mv 10.1158/1078-0432.CCR-17-0539
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1938606025</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2011381208</sourcerecordid><originalsourceid>FETCH-LOGICAL-c450t-7f5f141a5cccdcf69608046630c2e4b48fc6ba03fa5264acbacbc91cfca8308e3</originalsourceid><addsrcrecordid>eNpdkEtLw0AQgBdRbK3-BCXgxUvq7DMbbxKsLVQE0fOy2e7SlrzMJof8eze29SAMzDB88-BD6BbDHGMuHzEkMgZGyTzLPmKcxMBpeoammPMkpkTw81CfmAm68n4PgBkGdokmRMo0TRMyRWJVln1Vd1vb6maIaheth7LZ1qWOdLWJ3gZbhPopWmjT-d_Wsm6sv0YXThfe3hzzDH0tXj6zZbx-f11lz-vYMA5dnDjuwk3NjTEb40QqQAITgoIhluVMOiNyDdRpTgTTJg9hUmyc0ZKCtHSGHg57m7b-7q3vVLnzxhaFrmzde4VTKgUIIDyg9__Qfd23VfhOEcCYSkxABoofKNPW3rfWqabdlbodFAY1ilWjNDVKU0GswokaxYa5u-P2Pi_t5m_qZJL-AKX8cow</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2011381208</pqid></control><display><type>article</type><title>Immunotherapy of Lymphoma and Myeloma: Facts and Hopes</title><source>MEDLINE</source><source>American Association for Cancer Research</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Pianko, Matthew J ; Moskowitz, Alison J ; Lesokhin, Alexander M</creator><creatorcontrib>Pianko, Matthew J ; Moskowitz, Alison J ; Lesokhin, Alexander M</creatorcontrib><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. .</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-17-0539</identifier><identifier>PMID: 28899972</identifier><language>eng</language><publisher>United States: American Association for Cancer Research Inc</publisher><subject>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 &amp; 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</subject><ispartof>Clinical cancer research, 2018-03, Vol.24 (5), p.1002-1010</ispartof><rights>2017 American Association for Cancer Research.</rights><rights>Copyright American Association for Cancer Research Inc Mar 1, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-7f5f141a5cccdcf69608046630c2e4b48fc6ba03fa5264acbacbc91cfca8308e3</citedby><cites>FETCH-LOGICAL-c450t-7f5f141a5cccdcf69608046630c2e4b48fc6ba03fa5264acbacbc91cfca8308e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28899972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pianko, Matthew J</creatorcontrib><creatorcontrib>Moskowitz, Alison J</creatorcontrib><creatorcontrib>Lesokhin, Alexander M</creatorcontrib><title>Immunotherapy of Lymphoma and Myeloma: Facts and Hopes</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><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. .</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 &amp; 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 &amp; 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. .</abstract><cop>United States</cop><pub>American Association for Cancer Research Inc</pub><pmid>28899972</pmid><doi>10.1158/1078-0432.CCR-17-0539</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1078-0432
ispartof Clinical cancer research, 2018-03, Vol.24 (5), p.1002-1010
issn 1078-0432
1557-3265
language eng
recordid cdi_proquest_miscellaneous_1938606025
source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T23%3A04%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunotherapy%20of%20Lymphoma%20and%20Myeloma:%20Facts%20and%20Hopes&rft.jtitle=Clinical%20cancer%20research&rft.au=Pianko,%20Matthew%20J&rft.date=2018-03-01&rft.volume=24&rft.issue=5&rft.spage=1002&rft.epage=1010&rft.pages=1002-1010&rft.issn=1078-0432&rft.eissn=1557-3265&rft_id=info:doi/10.1158/1078-0432.CCR-17-0539&rft_dat=%3Cproquest_cross%3E2011381208%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2011381208&rft_id=info:pmid/28899972&rfr_iscdi=true