CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma
CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of...
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Veröffentlicht in: | Blood advances 2021-10, Vol.5 (20), p.4059-4063 |
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creator | Siddiqi, Tanya Wang, Xiuli Blanchard, M. Suzette Wagner, Jamie R. Popplewell, Leslie L. Budde, L. Elizabeth Stiller, Tracey L. Clark, Mary C. Lim, Laura Vyas, Vibhuti Brown, Christine E. Forman, Stephen J. |
description | CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity. CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity. Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade ≥ 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths. At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. This trial was registered at www.clinicaltrials.gov as #NCT02153580.
•CD19CAR T-cell therapy for patients with primary CNS lymphoma is feasible and safe.•This case series demonstrates that IV-delivered CD19CAR T cells are promising for the treatment of primary CNS lymphoma. |
doi_str_mv | 10.1182/bloodadvances.2020004106 |
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•CD19CAR T-cell therapy for patients with primary CNS lymphoma is feasible and safe.•This case series demonstrates that IV-delivered CD19CAR T cells are promising for the treatment of primary CNS lymphoma.</description><identifier>ISSN: 2473-9529</identifier><identifier>EISSN: 2473-9537</identifier><identifier>DOI: 10.1182/bloodadvances.2020004106</identifier><identifier>PMID: 34492703</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antigens, CD19 ; Humans ; Immunotherapy, Adoptive ; Lymphoma, Non-Hodgkin - therapy ; Receptors, Chimeric Antigen ; Stimulus Report ; T-Lymphocytes</subject><ispartof>Blood advances, 2021-10, Vol.5 (20), p.4059-4063</ispartof><rights>2021 American Society of Hematology</rights><rights>2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.</rights><rights>2021 by The American Society of Hematology. Licensed under , permitting only noncommercial, nonderivative use with attribution. All other rights reserved. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-26639798c1a3094e7dc5798c8d713be3900cd3090d2be7e60f5d0ffed76eaa403</citedby><cites>FETCH-LOGICAL-c479t-26639798c1a3094e7dc5798c8d713be3900cd3090d2be7e60f5d0ffed76eaa403</cites><orcidid>0000-0003-1464-5494 ; 0000-0001-5292-8298</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945630/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945630/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34492703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Siddiqi, Tanya</creatorcontrib><creatorcontrib>Wang, Xiuli</creatorcontrib><creatorcontrib>Blanchard, M. Suzette</creatorcontrib><creatorcontrib>Wagner, Jamie R.</creatorcontrib><creatorcontrib>Popplewell, Leslie L.</creatorcontrib><creatorcontrib>Budde, L. Elizabeth</creatorcontrib><creatorcontrib>Stiller, Tracey L.</creatorcontrib><creatorcontrib>Clark, Mary C.</creatorcontrib><creatorcontrib>Lim, Laura</creatorcontrib><creatorcontrib>Vyas, Vibhuti</creatorcontrib><creatorcontrib>Brown, Christine E.</creatorcontrib><creatorcontrib>Forman, Stephen J.</creatorcontrib><title>CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma</title><title>Blood advances</title><addtitle>Blood Adv</addtitle><description>CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity. CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity. Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade ≥ 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths. At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. This trial was registered at www.clinicaltrials.gov as #NCT02153580.
•CD19CAR T-cell therapy for patients with primary CNS lymphoma is feasible and safe.•This case series demonstrates that IV-delivered CD19CAR T cells are promising for the treatment of primary CNS lymphoma.</description><subject>Antigens, CD19</subject><subject>Humans</subject><subject>Immunotherapy, Adoptive</subject><subject>Lymphoma, Non-Hodgkin - therapy</subject><subject>Receptors, Chimeric Antigen</subject><subject>Stimulus Report</subject><subject>T-Lymphocytes</subject><issn>2473-9529</issn><issn>2473-9537</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkN1Kw0AQhRdRrNS-guwLpO5fstkboUarQlHQer1sdic2knTDJhb69qakVnvl1cww55wZPoQwJVNKU3adV9474zZmbaGdMsIIIYKS5ARdMCF5pGIuTw89UyM0advPXkRlwmPFztGIC6GYJPwCzbM7qiJXBrAdOJzNXvEyslBVuFtBMM0WFz7gLoDpalh32Be4CWVtwhZnz2-42tbNytfmEp0Vpmphsq9j9D6_X2aP0eLl4SmbLSIrpOoiliRcSZVaajhRAqSz8W5MnaQ8B64Isa7fEMdykJCQInakKMDJBIwRhI_RzZDbfOU1ONu_FEyl9y9pb0p9vFmXK_3hNzpVIk74LiAdAmzwbRugOHgp0Tu8-giv_sXbW6_-3j4Yf2D2gttBAD2BTQlBt7aEPmbAq50v_7_yDQ6ckVo</recordid><startdate>20211026</startdate><enddate>20211026</enddate><creator>Siddiqi, Tanya</creator><creator>Wang, Xiuli</creator><creator>Blanchard, M. Suzette</creator><creator>Wagner, Jamie R.</creator><creator>Popplewell, Leslie L.</creator><creator>Budde, L. Elizabeth</creator><creator>Stiller, Tracey L.</creator><creator>Clark, Mary C.</creator><creator>Lim, Laura</creator><creator>Vyas, Vibhuti</creator><creator>Brown, Christine E.</creator><creator>Forman, Stephen J.</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/0000-0003-1464-5494</orcidid><orcidid>https://orcid.org/0000-0001-5292-8298</orcidid></search><sort><creationdate>20211026</creationdate><title>CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma</title><author>Siddiqi, Tanya ; Wang, Xiuli ; Blanchard, M. Suzette ; Wagner, Jamie R. ; Popplewell, Leslie L. ; Budde, L. Elizabeth ; Stiller, Tracey L. ; Clark, Mary C. ; Lim, Laura ; Vyas, Vibhuti ; Brown, Christine E. ; Forman, Stephen J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-26639798c1a3094e7dc5798c8d713be3900cd3090d2be7e60f5d0ffed76eaa403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antigens, CD19</topic><topic>Humans</topic><topic>Immunotherapy, Adoptive</topic><topic>Lymphoma, Non-Hodgkin - therapy</topic><topic>Receptors, Chimeric Antigen</topic><topic>Stimulus Report</topic><topic>T-Lymphocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Siddiqi, Tanya</creatorcontrib><creatorcontrib>Wang, Xiuli</creatorcontrib><creatorcontrib>Blanchard, M. Suzette</creatorcontrib><creatorcontrib>Wagner, Jamie R.</creatorcontrib><creatorcontrib>Popplewell, Leslie L.</creatorcontrib><creatorcontrib>Budde, L. Elizabeth</creatorcontrib><creatorcontrib>Stiller, Tracey L.</creatorcontrib><creatorcontrib>Clark, Mary C.</creatorcontrib><creatorcontrib>Lim, Laura</creatorcontrib><creatorcontrib>Vyas, Vibhuti</creatorcontrib><creatorcontrib>Brown, Christine E.</creatorcontrib><creatorcontrib>Forman, Stephen J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Siddiqi, Tanya</au><au>Wang, Xiuli</au><au>Blanchard, M. Suzette</au><au>Wagner, Jamie R.</au><au>Popplewell, Leslie L.</au><au>Budde, L. Elizabeth</au><au>Stiller, Tracey L.</au><au>Clark, Mary C.</au><au>Lim, Laura</au><au>Vyas, Vibhuti</au><au>Brown, Christine E.</au><au>Forman, Stephen J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma</atitle><jtitle>Blood advances</jtitle><addtitle>Blood Adv</addtitle><date>2021-10-26</date><risdate>2021</risdate><volume>5</volume><issue>20</issue><spage>4059</spage><epage>4063</epage><pages>4059-4063</pages><issn>2473-9529</issn><eissn>2473-9537</eissn><abstract>CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity. CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity. Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade ≥ 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths. At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. This trial was registered at www.clinicaltrials.gov as #NCT02153580.
•CD19CAR T-cell therapy for patients with primary CNS lymphoma is feasible and safe.•This case series demonstrates that IV-delivered CD19CAR T cells are promising for the treatment of primary CNS lymphoma.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34492703</pmid><doi>10.1182/bloodadvances.2020004106</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-1464-5494</orcidid><orcidid>https://orcid.org/0000-0001-5292-8298</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, CD19 Humans Immunotherapy, Adoptive Lymphoma, Non-Hodgkin - therapy Receptors, Chimeric Antigen Stimulus Report T-Lymphocytes |
title | CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma |
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