Immune Checkpoint Inhibitors in Organ Transplant Patients
Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-asso...
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Veröffentlicht in: | Journal of immunotherapy (1997) 2017-09, Vol.40 (7), p.277-281 |
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creator | Kittai, Adam S Oldham, Hayden Cetnar, Jeremy Taylor, Matthew |
description | Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation. |
doi_str_mv | 10.1097/CJI.0000000000000180 |
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Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation.</description><identifier>ISSN: 1524-9557</identifier><identifier>EISSN: 1537-4513</identifier><identifier>DOI: 10.1097/CJI.0000000000000180</identifier><identifier>PMID: 28719552</identifier><language>eng</language><publisher>United States</publisher><subject>Aged ; Animals ; Antineoplastic Agents, Immunological - pharmacology ; Antineoplastic Agents, Immunological - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; B7-H1 Antigen - antagonists & inhibitors ; Combined Modality Therapy ; CTLA-4 Antigen - antagonists & inhibitors ; Disease Progression ; Female ; Humans ; Immunomodulation - drug effects ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Neoplasms, Second Primary - diagnosis ; Neoplasms, Second Primary - drug therapy ; Neoplasms, Second Primary - etiology ; Organ Transplantation - adverse effects ; Programmed Cell Death 1 Receptor - antagonists & inhibitors ; T-Lymphocyte Subsets - drug effects ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; Transplant Recipients ; Treatment Outcome</subject><ispartof>Journal of immunotherapy (1997), 2017-09, Vol.40 (7), p.277-281</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-efc6291bc973f894c79f2696512b6c5d4c73abe88fc5723e5cd7573e17131023</citedby><cites>FETCH-LOGICAL-c373t-efc6291bc973f894c79f2696512b6c5d4c73abe88fc5723e5cd7573e17131023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28719552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kittai, Adam S</creatorcontrib><creatorcontrib>Oldham, Hayden</creatorcontrib><creatorcontrib>Cetnar, Jeremy</creatorcontrib><creatorcontrib>Taylor, Matthew</creatorcontrib><title>Immune Checkpoint Inhibitors in Organ Transplant Patients</title><title>Journal of immunotherapy (1997)</title><addtitle>J Immunother</addtitle><description>Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation.</description><subject>Aged</subject><subject>Animals</subject><subject>Antineoplastic Agents, Immunological - pharmacology</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>B7-H1 Antigen - antagonists & inhibitors</subject><subject>Combined Modality Therapy</subject><subject>CTLA-4 Antigen - antagonists & inhibitors</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Immunomodulation - drug effects</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Neoplasms, Second Primary - diagnosis</subject><subject>Neoplasms, Second Primary - drug therapy</subject><subject>Neoplasms, Second Primary - etiology</subject><subject>Organ Transplantation - adverse effects</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>T-Lymphocyte Subsets - drug effects</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>Transplant Recipients</subject><subject>Treatment Outcome</subject><issn>1524-9557</issn><issn>1537-4513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkMtOwzAQRS0EoqXwBwhlySbFY8dxvEQRj6BKZZG95bgONTROsJMFf4-rFoSYzYzu3HnoIHQNeAlY8LvypVrivwEFPkFzYJSnGQN6uq9JlgrG-AxdhPCOMclJRs7RjBQcok7mSFRdNzmTlFujP4beujGp3NY2dux9SKxL1v5NuaT2yoVhp2L7VY3WuDFcorNW7YK5OuYFqh8f6vI5Xa2fqvJ-lWrK6ZiaVudEQKMFp20hMs1FS3KRMyBNrtkmClQ1pihazTihhukNZ5wa4EABE7pAt4e1g-8_JxNG2dmgzS7-YvopSBAEUwGcF9GaHaza9yF408rB2075LwlY7pnJyEz-ZxbHbo4XpqYzm9-hH0j0GzG0ZbU</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Kittai, Adam S</creator><creator>Oldham, Hayden</creator><creator>Cetnar, Jeremy</creator><creator>Taylor, Matthew</creator><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>7X8</scope></search><sort><creationdate>20170901</creationdate><title>Immune Checkpoint Inhibitors in Organ Transplant Patients</title><author>Kittai, Adam S ; Oldham, Hayden ; Cetnar, Jeremy ; Taylor, Matthew</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-efc6291bc973f894c79f2696512b6c5d4c73abe88fc5723e5cd7573e17131023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Animals</topic><topic>Antineoplastic Agents, Immunological - pharmacology</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>B7-H1 Antigen - antagonists & inhibitors</topic><topic>Combined Modality Therapy</topic><topic>CTLA-4 Antigen - antagonists & inhibitors</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Immunomodulation - drug effects</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Neoplasms, Second Primary - diagnosis</topic><topic>Neoplasms, Second Primary - drug therapy</topic><topic>Neoplasms, Second Primary - etiology</topic><topic>Organ Transplantation - adverse effects</topic><topic>Programmed Cell Death 1 Receptor - antagonists & inhibitors</topic><topic>T-Lymphocyte Subsets - drug effects</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - metabolism</topic><topic>Transplant Recipients</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kittai, Adam S</creatorcontrib><creatorcontrib>Oldham, Hayden</creatorcontrib><creatorcontrib>Cetnar, Jeremy</creatorcontrib><creatorcontrib>Taylor, Matthew</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunotherapy (1997)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kittai, Adam S</au><au>Oldham, Hayden</au><au>Cetnar, Jeremy</au><au>Taylor, Matthew</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune Checkpoint Inhibitors in Organ Transplant Patients</atitle><jtitle>Journal of immunotherapy (1997)</jtitle><addtitle>J Immunother</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>40</volume><issue>7</issue><spage>277</spage><epage>281</epage><pages>277-281</pages><issn>1524-9557</issn><eissn>1537-4513</eissn><abstract>Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation.</abstract><cop>United States</cop><pmid>28719552</pmid><doi>10.1097/CJI.0000000000000180</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Animals Antineoplastic Agents, Immunological - pharmacology Antineoplastic Agents, Immunological - therapeutic use Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use B7-H1 Antigen - antagonists & inhibitors Combined Modality Therapy CTLA-4 Antigen - antagonists & inhibitors Disease Progression Female Humans Immunomodulation - drug effects Immunosuppressive Agents - adverse effects Immunosuppressive Agents - therapeutic use Neoplasms, Second Primary - diagnosis Neoplasms, Second Primary - drug therapy Neoplasms, Second Primary - etiology Organ Transplantation - adverse effects Programmed Cell Death 1 Receptor - antagonists & inhibitors T-Lymphocyte Subsets - drug effects T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism Transplant Recipients Treatment Outcome |
title | Immune Checkpoint Inhibitors in Organ Transplant Patients |
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