PD-1 blockade for relapsed lymphoma post–allogeneic hematopoietic cell transplant: high response rate but frequent GVHD
Given the limited treatment options for relapsed lymphoma post–allogeneic hematopoietic cell transplantation (post–allo-HCT) and the success of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti–PD-1 monoclonal antibodies (mAbs) are increasingly being used off-labe...
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creator | Haverkos, Bradley M. Abbott, Diana Hamadani, Mehdi Armand, Philippe Flowers, Mary E. Merryman, Reid Kamdar, Manali Kanate, Abraham Sebastian Saad, Ayman Mehta, Amitkumar Ganguly, Siddhartha Fenske, Timothy S. Hari, Parameswaran Lowsky, Robert Andritsos, Leslie Jagasia, Madan Bashey, Asad Brown, Stacey Bachanova, Veronika Stephens, Deborah Mineishi, Shin Nakamura, Ryotaro Chen, Yi-Bin Blazar, Bruce R. Gutman, Jonathan Devine, Steven M. |
description | Given the limited treatment options for relapsed lymphoma post–allogeneic hematopoietic cell transplantation (post–allo-HCT) and the success of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti–PD-1 monoclonal antibodies (mAbs) are increasingly being used off-label after allo-HCT. To characterize the safety and efficacy of PD-1 blockade in this setting, we conducted a multicenter retrospective analysis of 31 lymphoma patients receiving anti–PD-1 mAbs for relapse post–allo-HCT. Twenty-nine (94%) patients had cHL and 27 had ≥1 salvage therapy post–allo-HCT and prior to anti–PD-1 treatment. Median follow-up was 428 days (range, 133-833) after the first dose of anti–PD-1. Overall response rate was 77% (15 complete responses and 8 partial responses) in 30 evaluable patients. At last follow-up, 11 of 31 patients progressed and 21 of 31 (68%) remain alive, with 8 (26%) deaths related to new-onset graft-versus-host disease (GVHD) after anti–PD-1. Seventeen (55%) patients developed treatment-emergent GVHD after initiation of anti–PD-1 (6 acute, 4 overlap, and 7 chronic), with onset after a median of 1, 2, and 2 doses, respectively. GVHD severity was grade III-IV acute or severe chronic in 9 patients. Only 2 of these 17 patients achieved complete response to GVHD treatment, and 14 of 17 required ≥2 systemic therapies. In conclusion, PD-1 blockade in relapsed cHL allo-HCT patients appears to be highly efficacious but frequently complicated by rapid onset of severe and treatment-refractory GVHD. PD-1 blockade post–allo-HCT should be studied further but cannot be recommended for routine use outside of a clinical trial.
•Checkpoint blockade via anti–PD-1 mAbs was associated with a high overall response rate in relapsed Hodgkin lymphoma allo-HCT patients.•Checkpoint blockade via anti–PD-1 mAbs after allo-HCT can be complicated by rapid onset of severe and treatment-refractory GVHD. |
doi_str_mv | 10.1182/blood-2017-01-761346 |
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•Checkpoint blockade via anti–PD-1 mAbs was associated with a high overall response rate in relapsed Hodgkin lymphoma allo-HCT patients.•Checkpoint blockade via anti–PD-1 mAbs after allo-HCT can be complicated by rapid onset of severe and treatment-refractory GVHD.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2017-01-761346</identifier><identifier>PMID: 28468799</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal, Humanized - administration & dosage ; Antibodies, Monoclonal, Humanized - adverse effects ; Antineoplastic Agents - therapeutic use ; Female ; Gene Expression ; Graft vs Host Disease - chemically induced ; Graft vs Host Disease - immunology ; Graft vs Host Disease - mortality ; Graft vs Host Disease - pathology ; Hematopoietic Stem Cell Transplantation ; Hodgkin Disease - immunology ; Hodgkin Disease - mortality ; Hodgkin Disease - pathology ; Hodgkin Disease - therapy ; Humans ; Male ; Middle Aged ; Neoplasm Recurrence, Local ; Nivolumab ; Programmed Cell Death 1 Receptor - antagonists & inhibitors ; Programmed Cell Death 1 Receptor - genetics ; Programmed Cell Death 1 Receptor - immunology ; Remission Induction ; Retrospective Studies ; Salvage Therapy - methods ; Survival Analysis ; Transplantation ; Transplantation Conditioning ; Transplantation, Homologous ; Treatment Outcome</subject><ispartof>Blood, 2017-07, Vol.130 (2), p.221-228</ispartof><rights>2017 American Society of Hematology</rights><rights>2017 by The American Society of Hematology.</rights><rights>2017 by The American Society of Hematology 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-8a5eb3c4ddf57a62aa89da142049874ffd716526868e1bf44073c759f5b5e9003</citedby><cites>FETCH-LOGICAL-c580t-8a5eb3c4ddf57a62aa89da142049874ffd716526868e1bf44073c759f5b5e9003</cites><orcidid>0000-0002-3872-0615</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28468799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haverkos, Bradley M.</creatorcontrib><creatorcontrib>Abbott, Diana</creatorcontrib><creatorcontrib>Hamadani, Mehdi</creatorcontrib><creatorcontrib>Armand, Philippe</creatorcontrib><creatorcontrib>Flowers, Mary E.</creatorcontrib><creatorcontrib>Merryman, Reid</creatorcontrib><creatorcontrib>Kamdar, Manali</creatorcontrib><creatorcontrib>Kanate, Abraham Sebastian</creatorcontrib><creatorcontrib>Saad, Ayman</creatorcontrib><creatorcontrib>Mehta, Amitkumar</creatorcontrib><creatorcontrib>Ganguly, Siddhartha</creatorcontrib><creatorcontrib>Fenske, Timothy S.</creatorcontrib><creatorcontrib>Hari, Parameswaran</creatorcontrib><creatorcontrib>Lowsky, Robert</creatorcontrib><creatorcontrib>Andritsos, Leslie</creatorcontrib><creatorcontrib>Jagasia, Madan</creatorcontrib><creatorcontrib>Bashey, Asad</creatorcontrib><creatorcontrib>Brown, Stacey</creatorcontrib><creatorcontrib>Bachanova, Veronika</creatorcontrib><creatorcontrib>Stephens, Deborah</creatorcontrib><creatorcontrib>Mineishi, Shin</creatorcontrib><creatorcontrib>Nakamura, Ryotaro</creatorcontrib><creatorcontrib>Chen, Yi-Bin</creatorcontrib><creatorcontrib>Blazar, Bruce R.</creatorcontrib><creatorcontrib>Gutman, Jonathan</creatorcontrib><creatorcontrib>Devine, Steven M.</creatorcontrib><title>PD-1 blockade for relapsed lymphoma post–allogeneic hematopoietic cell transplant: high response rate but frequent GVHD</title><title>Blood</title><addtitle>Blood</addtitle><description>Given the limited treatment options for relapsed lymphoma post–allogeneic hematopoietic cell transplantation (post–allo-HCT) and the success of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti–PD-1 monoclonal antibodies (mAbs) are increasingly being used off-label after allo-HCT. To characterize the safety and efficacy of PD-1 blockade in this setting, we conducted a multicenter retrospective analysis of 31 lymphoma patients receiving anti–PD-1 mAbs for relapse post–allo-HCT. Twenty-nine (94%) patients had cHL and 27 had ≥1 salvage therapy post–allo-HCT and prior to anti–PD-1 treatment. Median follow-up was 428 days (range, 133-833) after the first dose of anti–PD-1. Overall response rate was 77% (15 complete responses and 8 partial responses) in 30 evaluable patients. At last follow-up, 11 of 31 patients progressed and 21 of 31 (68%) remain alive, with 8 (26%) deaths related to new-onset graft-versus-host disease (GVHD) after anti–PD-1. Seventeen (55%) patients developed treatment-emergent GVHD after initiation of anti–PD-1 (6 acute, 4 overlap, and 7 chronic), with onset after a median of 1, 2, and 2 doses, respectively. GVHD severity was grade III-IV acute or severe chronic in 9 patients. Only 2 of these 17 patients achieved complete response to GVHD treatment, and 14 of 17 required ≥2 systemic therapies. In conclusion, PD-1 blockade in relapsed cHL allo-HCT patients appears to be highly efficacious but frequently complicated by rapid onset of severe and treatment-refractory GVHD. PD-1 blockade post–allo-HCT should be studied further but cannot be recommended for routine use outside of a clinical trial.
•Checkpoint blockade via anti–PD-1 mAbs was associated with a high overall response rate in relapsed Hodgkin lymphoma allo-HCT patients.•Checkpoint blockade via anti–PD-1 mAbs after allo-HCT can be complicated by rapid onset of severe and treatment-refractory GVHD.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal, Humanized - administration & dosage</subject><subject>Antibodies, Monoclonal, Humanized - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Graft vs Host Disease - chemically induced</subject><subject>Graft vs Host Disease - immunology</subject><subject>Graft vs Host Disease - mortality</subject><subject>Graft vs Host Disease - pathology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hodgkin Disease - immunology</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin Disease - therapy</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local</subject><subject>Nivolumab</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>Programmed Cell Death 1 Receptor - genetics</subject><subject>Programmed Cell Death 1 Receptor - immunology</subject><subject>Remission Induction</subject><subject>Retrospective Studies</subject><subject>Salvage Therapy - methods</subject><subject>Survival Analysis</subject><subject>Transplantation</subject><subject>Transplantation Conditioning</subject><subject>Transplantation, Homologous</subject><subject>Treatment Outcome</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQhi0EokvhDRDyC4SOEzt2OCChFlqkSnAArpZjTzYGJw62t9LeeAfekCdploUCF06j0ej__pn5CXnK4Dljqj7rQ4yuqoHJClglW9bw9h7ZMFGrCqCG-2QDAG3FO8lOyKOcPwMw3tTiITmpFW-V7LoN2b-_qBhdWfaLcUiHmGjCYJaMjob9tIxxMnSJufz49t2EELc4o7d0xMmUuESPZe0shkBLMnNegpnLCzr67bhy8hLnjDSZgrTfFTok_LrDudDLT1cXj8mDwYSMT37VU_LxzesP51fV9bvLt-evrisrFJRKGYF9Y7lzg5CmrY1RnTOM18A7JfkwOMlaUbeqVcj6gXOQjZWiG0QvsANoTsnLI3fZ9RM6u_onE_SS_GTSXkfj9b-T2Y96G2-0EAxkdwDwI8CmmHPC4U7LQB-i0D-j0IcoNDB9jGKVPfvb9070-_d_FsP1-huPSWfrcbbofEJbtIv-_w63tcefCQ</recordid><startdate>20170713</startdate><enddate>20170713</enddate><creator>Haverkos, Bradley M.</creator><creator>Abbott, Diana</creator><creator>Hamadani, Mehdi</creator><creator>Armand, Philippe</creator><creator>Flowers, Mary E.</creator><creator>Merryman, Reid</creator><creator>Kamdar, Manali</creator><creator>Kanate, Abraham Sebastian</creator><creator>Saad, Ayman</creator><creator>Mehta, Amitkumar</creator><creator>Ganguly, Siddhartha</creator><creator>Fenske, Timothy S.</creator><creator>Hari, Parameswaran</creator><creator>Lowsky, Robert</creator><creator>Andritsos, Leslie</creator><creator>Jagasia, Madan</creator><creator>Bashey, Asad</creator><creator>Brown, Stacey</creator><creator>Bachanova, Veronika</creator><creator>Stephens, Deborah</creator><creator>Mineishi, Shin</creator><creator>Nakamura, Ryotaro</creator><creator>Chen, Yi-Bin</creator><creator>Blazar, Bruce R.</creator><creator>Gutman, Jonathan</creator><creator>Devine, Steven M.</creator><general>Elsevier Inc</general><general>American Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><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>5PM</scope><orcidid>https://orcid.org/0000-0002-3872-0615</orcidid></search><sort><creationdate>20170713</creationdate><title>PD-1 blockade for relapsed lymphoma post–allogeneic hematopoietic cell transplant: high response rate but frequent GVHD</title><author>Haverkos, Bradley M. ; Abbott, Diana ; Hamadani, Mehdi ; Armand, Philippe ; Flowers, Mary E. ; Merryman, Reid ; Kamdar, Manali ; Kanate, Abraham Sebastian ; Saad, Ayman ; Mehta, Amitkumar ; Ganguly, Siddhartha ; Fenske, Timothy S. ; Hari, Parameswaran ; Lowsky, Robert ; Andritsos, Leslie ; Jagasia, Madan ; Bashey, Asad ; Brown, Stacey ; Bachanova, Veronika ; Stephens, Deborah ; Mineishi, Shin ; Nakamura, Ryotaro ; Chen, Yi-Bin ; Blazar, Bruce R. ; Gutman, Jonathan ; Devine, Steven M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-8a5eb3c4ddf57a62aa89da142049874ffd716526868e1bf44073c759f5b5e9003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - 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To characterize the safety and efficacy of PD-1 blockade in this setting, we conducted a multicenter retrospective analysis of 31 lymphoma patients receiving anti–PD-1 mAbs for relapse post–allo-HCT. Twenty-nine (94%) patients had cHL and 27 had ≥1 salvage therapy post–allo-HCT and prior to anti–PD-1 treatment. Median follow-up was 428 days (range, 133-833) after the first dose of anti–PD-1. Overall response rate was 77% (15 complete responses and 8 partial responses) in 30 evaluable patients. At last follow-up, 11 of 31 patients progressed and 21 of 31 (68%) remain alive, with 8 (26%) deaths related to new-onset graft-versus-host disease (GVHD) after anti–PD-1. Seventeen (55%) patients developed treatment-emergent GVHD after initiation of anti–PD-1 (6 acute, 4 overlap, and 7 chronic), with onset after a median of 1, 2, and 2 doses, respectively. GVHD severity was grade III-IV acute or severe chronic in 9 patients. Only 2 of these 17 patients achieved complete response to GVHD treatment, and 14 of 17 required ≥2 systemic therapies. In conclusion, PD-1 blockade in relapsed cHL allo-HCT patients appears to be highly efficacious but frequently complicated by rapid onset of severe and treatment-refractory GVHD. PD-1 blockade post–allo-HCT should be studied further but cannot be recommended for routine use outside of a clinical trial.
•Checkpoint blockade via anti–PD-1 mAbs was associated with a high overall response rate in relapsed Hodgkin lymphoma allo-HCT patients.•Checkpoint blockade via anti–PD-1 mAbs after allo-HCT can be complicated by rapid onset of severe and treatment-refractory GVHD.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28468799</pmid><doi>10.1182/blood-2017-01-761346</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3872-0615</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal, Humanized - administration & dosage Antibodies, Monoclonal, Humanized - adverse effects Antineoplastic Agents - therapeutic use Female Gene Expression Graft vs Host Disease - chemically induced Graft vs Host Disease - immunology Graft vs Host Disease - mortality Graft vs Host Disease - pathology Hematopoietic Stem Cell Transplantation Hodgkin Disease - immunology Hodgkin Disease - mortality Hodgkin Disease - pathology Hodgkin Disease - therapy Humans Male Middle Aged Neoplasm Recurrence, Local Nivolumab Programmed Cell Death 1 Receptor - antagonists & inhibitors Programmed Cell Death 1 Receptor - genetics Programmed Cell Death 1 Receptor - immunology Remission Induction Retrospective Studies Salvage Therapy - methods Survival Analysis Transplantation Transplantation Conditioning Transplantation, Homologous Treatment Outcome |
title | PD-1 blockade for relapsed lymphoma post–allogeneic hematopoietic cell transplant: high response rate but frequent GVHD |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T04%3A54%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PD-1%20blockade%20for%20relapsed%20lymphoma%20post%E2%80%93allogeneic%20hematopoietic%20cell%20transplant:%20high%20response%20rate%20but%20frequent%20GVHD&rft.jtitle=Blood&rft.au=Haverkos,%20Bradley%20M.&rft.date=2017-07-13&rft.volume=130&rft.issue=2&rft.spage=221&rft.epage=228&rft.pages=221-228&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood-2017-01-761346&rft_dat=%3Cpubmed_cross%3E28468799%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/28468799&rft_els_id=S0006497120332225&rfr_iscdi=true |