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Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS

BackgroundChimeric antigen receptor (CAR) T cell therapy is an advanced and effective immunotherapy for relapsed or refractory B-cell malignancies. High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a...

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Published in:Journal for immunotherapy of cancer 2023-11, Vol.11 (11), p.e007790
Main Authors: Zhang, Man, Long, Xiaolu, Xiao, Yi, Jin, Jin, Chen, Caixia, Meng, Jiao, Liu, Wanying, Liu, Aichun, Chen, Liting
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container_title Journal for immunotherapy of cancer
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Long, Xiaolu
Xiao, Yi
Jin, Jin
Chen, Caixia
Meng, Jiao
Liu, Wanying
Liu, Aichun
Chen, Liting
description BackgroundChimeric antigen receptor (CAR) T cell therapy is an advanced and effective immunotherapy for relapsed or refractory B-cell malignancies. High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a high frequency of adverse events, such as cytokine release syndrome (CRS), which affects its efficacy and can even be life-threatening. At present, a variety of markers associated with clinical response and treatment toxicity after CAR T cells infusion have been reported. Although these biomarkers can act as effective indicators reflecting CAR T cells expansion as well as CRS, they fail to predict the expansion rate of CAR T cells. Hence, further investigation is urgent to find a new biomarker to fill this void.MethodsWe analyzed the association between the absolute neutrophil count (ANC) and CAR expansion and CRS in 45 patients with B-cell malignancies from two clinical trials. We proposed that ANC could be a practical biomarker for CAR T cells expansion and CRS, and conducted a feasibility analysis on its predictive ability.ResultsIn this study, 17 B-cell hematological malignancy patients with anti-B-cell maturation antigen CAR-treated and 28 with CAR19/22 T-cell-treated were enrolled and divided into an ANC-absence group and an ANC-presence group. The results showed that ANC absence correlated positively with CAR expansion and the expansion rate. The ANC can be used as a predictive marker for CAR T cells expansion. Moreover, the patients with ANC absence experienced a more severe CRS, and ANC performed a predictive ability for CRS. In addition, the peak serum concentration of several cytokines involved in CRS was higher in patients with ANC absence.ConclusionThus, we suggest ANC as an evaluative and predictive biomarker for CAR expansion and CRS during CAR T cell therapy, which can help to maximize clinical efficacy, reduce treatment-related toxicity and prolong survival.
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High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a high frequency of adverse events, such as cytokine release syndrome (CRS), which affects its efficacy and can even be life-threatening. At present, a variety of markers associated with clinical response and treatment toxicity after CAR T cells infusion have been reported. Although these biomarkers can act as effective indicators reflecting CAR T cells expansion as well as CRS, they fail to predict the expansion rate of CAR T cells. Hence, further investigation is urgent to find a new biomarker to fill this void.MethodsWe analyzed the association between the absolute neutrophil count (ANC) and CAR expansion and CRS in 45 patients with B-cell malignancies from two clinical trials. We proposed that ANC could be a practical biomarker for CAR T cells expansion and CRS, and conducted a feasibility analysis on its predictive ability.ResultsIn this study, 17 B-cell hematological malignancy patients with anti-B-cell maturation antigen CAR-treated and 28 with CAR19/22 T-cell-treated were enrolled and divided into an ANC-absence group and an ANC-presence group. The results showed that ANC absence correlated positively with CAR expansion and the expansion rate. The ANC can be used as a predictive marker for CAR T cells expansion. Moreover, the patients with ANC absence experienced a more severe CRS, and ANC performed a predictive ability for CRS. In addition, the peak serum concentration of several cytokines involved in CRS was higher in patients with ANC absence.ConclusionThus, we suggest ANC as an evaluative and predictive biomarker for CAR expansion and CRS during CAR T cell therapy, which can help to maximize clinical efficacy, reduce treatment-related toxicity and prolong survival.</description><identifier>ISSN: 2051-1426</identifier><identifier>EISSN: 2051-1426</identifier><identifier>DOI: 10.1136/jitc-2023-007790</identifier><identifier>PMID: 38016717</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>Anticoagulants ; Antigens ; Bacterial infections ; Biomarkers ; Cancer ; Cells ; Chemotherapy ; Clinical trials ; Cytokine Release Syndrome ; Cytokines ; Humans ; Immunotherapy ; Immunotherapy Biomarkers ; Lymphocytes ; Neoplasms ; Neutropenia ; Neutrophils ; Patients ; Receptors, Antigen, T-Cell - genetics ; T-Lymphocytes ; Toxicity ; Variables</subject><ispartof>Journal for immunotherapy of cancer, 2023-11, Vol.11 (11), p.e007790</ispartof><rights>Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2023 Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-b481t-c8d065975046595d13f4235cb094c33abef9247ecdc416a5378abbac2d9505ec3</cites><orcidid>0000-0002-7786-1226 ; 0000-0001-8552-2665</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2894249967/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2894249967?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,55328,74872,77406,77432</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38016717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Man</creatorcontrib><creatorcontrib>Long, Xiaolu</creatorcontrib><creatorcontrib>Xiao, Yi</creatorcontrib><creatorcontrib>Jin, Jin</creatorcontrib><creatorcontrib>Chen, Caixia</creatorcontrib><creatorcontrib>Meng, Jiao</creatorcontrib><creatorcontrib>Liu, Wanying</creatorcontrib><creatorcontrib>Liu, Aichun</creatorcontrib><creatorcontrib>Chen, Liting</creatorcontrib><title>Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS</title><title>Journal for immunotherapy of cancer</title><addtitle>J Immunother Cancer</addtitle><addtitle>J Immunother Cancer</addtitle><description>BackgroundChimeric antigen receptor (CAR) T cell therapy is an advanced and effective immunotherapy for relapsed or refractory B-cell malignancies. High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a high frequency of adverse events, such as cytokine release syndrome (CRS), which affects its efficacy and can even be life-threatening. At present, a variety of markers associated with clinical response and treatment toxicity after CAR T cells infusion have been reported. Although these biomarkers can act as effective indicators reflecting CAR T cells expansion as well as CRS, they fail to predict the expansion rate of CAR T cells. Hence, further investigation is urgent to find a new biomarker to fill this void.MethodsWe analyzed the association between the absolute neutrophil count (ANC) and CAR expansion and CRS in 45 patients with B-cell malignancies from two clinical trials. We proposed that ANC could be a practical biomarker for CAR T cells expansion and CRS, and conducted a feasibility analysis on its predictive ability.ResultsIn this study, 17 B-cell hematological malignancy patients with anti-B-cell maturation antigen CAR-treated and 28 with CAR19/22 T-cell-treated were enrolled and divided into an ANC-absence group and an ANC-presence group. The results showed that ANC absence correlated positively with CAR expansion and the expansion rate. The ANC can be used as a predictive marker for CAR T cells expansion. Moreover, the patients with ANC absence experienced a more severe CRS, and ANC performed a predictive ability for CRS. In addition, the peak serum concentration of several cytokines involved in CRS was higher in patients with ANC absence.ConclusionThus, we suggest ANC as an evaluative and predictive biomarker for CAR expansion and CRS during CAR T cell therapy, which can help to maximize clinical efficacy, reduce treatment-related toxicity and prolong survival.</description><subject>Anticoagulants</subject><subject>Antigens</subject><subject>Bacterial infections</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cells</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Cytokine Release Syndrome</subject><subject>Cytokines</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Immunotherapy Biomarkers</subject><subject>Lymphocytes</subject><subject>Neoplasms</subject><subject>Neutropenia</subject><subject>Neutrophils</subject><subject>Patients</subject><subject>Receptors, Antigen, T-Cell - genetics</subject><subject>T-Lymphocytes</subject><subject>Toxicity</subject><subject>Variables</subject><issn>2051-1426</issn><issn>2051-1426</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kstrFTEUxgdRbKndu5KAGxeO5jnJrORysVooCLWuQ17Tm2HuZEwyF7vzT2-mU2sruEpy8p3fefBV1WsEPyBEmo-9z6bGEJMaQs5b-Kw6xpChGlHcPH90P6pOU-ohhAgSIoR4WR0RAVHDET-ufm9Scint3ZiBGi2YorPeZH9wQGk_-HwDQgfybnmmMMzZgdHNOYZp5wdgwlzy_AgmF_20c1ENQA8hWNCFuMQP_hDAdnMJroBxw5CA-zWpMfkw3lXbXn5_Vb3o1JDc6f15Uv04-3y1_VpffPtyvt1c1JoKlGsjLGxYyxmk5WAWkY5iwoyGLTWEKO26FlPujDUUNYoRLpTWymDbMsicISfV-cq1QfVyin6v4o0Mysu7QIjXUsXszeAkKwjBCdfQWKoRFZZiLRjTJdwiowvr08qaZr131pTllcmfQJ_-jH4nr8NBItiI0j0phHf3hBh-zi5lufdp2ZAaXZiTxKJlmLUCiyJ9-4-0D3Mcy64WFcW0bRteVHBVmRhSiq576AZBudhFLnaRi13kapeS8ubxFA8Jf8xRBO9Xgd73f4v-l3cLwgfKAw</recordid><startdate>20231127</startdate><enddate>20231127</enddate><creator>Zhang, Man</creator><creator>Long, Xiaolu</creator><creator>Xiao, Yi</creator><creator>Jin, Jin</creator><creator>Chen, Caixia</creator><creator>Meng, Jiao</creator><creator>Liu, Wanying</creator><creator>Liu, Aichun</creator><creator>Chen, Liting</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7786-1226</orcidid><orcidid>https://orcid.org/0000-0001-8552-2665</orcidid></search><sort><creationdate>20231127</creationdate><title>Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS</title><author>Zhang, Man ; 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High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a high frequency of adverse events, such as cytokine release syndrome (CRS), which affects its efficacy and can even be life-threatening. At present, a variety of markers associated with clinical response and treatment toxicity after CAR T cells infusion have been reported. Although these biomarkers can act as effective indicators reflecting CAR T cells expansion as well as CRS, they fail to predict the expansion rate of CAR T cells. Hence, further investigation is urgent to find a new biomarker to fill this void.MethodsWe analyzed the association between the absolute neutrophil count (ANC) and CAR expansion and CRS in 45 patients with B-cell malignancies from two clinical trials. We proposed that ANC could be a practical biomarker for CAR T cells expansion and CRS, and conducted a feasibility analysis on its predictive ability.ResultsIn this study, 17 B-cell hematological malignancy patients with anti-B-cell maturation antigen CAR-treated and 28 with CAR19/22 T-cell-treated were enrolled and divided into an ANC-absence group and an ANC-presence group. The results showed that ANC absence correlated positively with CAR expansion and the expansion rate. The ANC can be used as a predictive marker for CAR T cells expansion. Moreover, the patients with ANC absence experienced a more severe CRS, and ANC performed a predictive ability for CRS. In addition, the peak serum concentration of several cytokines involved in CRS was higher in patients with ANC absence.ConclusionThus, we suggest ANC as an evaluative and predictive biomarker for CAR expansion and CRS during CAR T cell therapy, which can help to maximize clinical efficacy, reduce treatment-related toxicity and prolong survival.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>38016717</pmid><doi>10.1136/jitc-2023-007790</doi><orcidid>https://orcid.org/0000-0002-7786-1226</orcidid><orcidid>https://orcid.org/0000-0001-8552-2665</orcidid><oa>free_for_read</oa></addata></record>
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subjects Anticoagulants
Antigens
Bacterial infections
Biomarkers
Cancer
Cells
Chemotherapy
Clinical trials
Cytokine Release Syndrome
Cytokines
Humans
Immunotherapy
Immunotherapy Biomarkers
Lymphocytes
Neoplasms
Neutropenia
Neutrophils
Patients
Receptors, Antigen, T-Cell - genetics
T-Lymphocytes
Toxicity
Variables
title Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS
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