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Geographic and Racial Disparities in Chimeric Antigen Receptor–T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma
We investigate the geographical and racial disparities in accessing CAR-T and bispecific antibodies trials for DLBCL. ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS versi...
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Published in: | Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2024-05, Vol.24 (5), p.316-322 |
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container_title | Clinical lymphoma, myeloma and leukemia |
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description | We investigate the geographical and racial disparities in accessing CAR-T and bispecific antibodies trials for DLBCL.
ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS version 26 was used for analysis.
There were 62 CAR-T and 13 bispecific antibodies trials with 6221 enrolled or expected to enroll patients. Eighty-five percent of the clinical trials were only open in the US, and the majority 64% were pharmaceutical-funded. There were 126 unique study sites distributed over 31 states with 11 (0-51) mean number of trials per state and 4.5 (1-26) and 4.4 (1-24) mean number of CAR-T and bispecific antibodies trials per site, respectively. Southern states had the most number of trials 31%, followed by Midwestern 25%, Northeastern 24%, and Western 20%. The highest number of study locations were in California 13, New York 9, and Pennsylvania 9, while the highest number of open studies were in California 51, Texas 32, and New York 23. Twenty states had no open CAR-T or bispecific antibodies trials. Only 33% of African Americans (AA) lived in a county with a trial, and 7 out of 10 states with the highest proportion of AA residents (18.6%-41.4%) have no or less than 4 trial sites. Of the 62 counties analyzed, 92% were White predominant, while only 8% were AA predominant (P = .009).
Strategies should be framed to address the observed disparities and to improve access. |
doi_str_mv | 10.1016/j.clml.2024.01.006 |
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ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS version 26 was used for analysis.
There were 62 CAR-T and 13 bispecific antibodies trials with 6221 enrolled or expected to enroll patients. Eighty-five percent of the clinical trials were only open in the US, and the majority 64% were pharmaceutical-funded. There were 126 unique study sites distributed over 31 states with 11 (0-51) mean number of trials per state and 4.5 (1-26) and 4.4 (1-24) mean number of CAR-T and bispecific antibodies trials per site, respectively. Southern states had the most number of trials 31%, followed by Midwestern 25%, Northeastern 24%, and Western 20%. The highest number of study locations were in California 13, New York 9, and Pennsylvania 9, while the highest number of open studies were in California 51, Texas 32, and New York 23. Twenty states had no open CAR-T or bispecific antibodies trials. Only 33% of African Americans (AA) lived in a county with a trial, and 7 out of 10 states with the highest proportion of AA residents (18.6%-41.4%) have no or less than 4 trial sites. Of the 62 counties analyzed, 92% were White predominant, while only 8% were AA predominant (P = .009).
Strategies should be framed to address the observed disparities and to improve access.</description><identifier>ISSN: 2152-2650</identifier><identifier>EISSN: 2152-2669</identifier><identifier>DOI: 10.1016/j.clml.2024.01.006</identifier><identifier>PMID: 38342727</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antibodies, Bispecific - therapeutic use ; CAR-T Cell ; Clinical Trials ; Clinical Trials as Topic ; Geographical Disparities ; Health Services Accessibility - statistics & numerical data ; Healthcare Disparities - statistics & numerical data ; Humans ; Immunotherapy, Adoptive - methods ; Lymphoma, Large B-Cell, Diffuse - immunology ; Lymphoma, Large B-Cell, Diffuse - therapy ; Receptors, Chimeric Antigen - immunology ; Receptors, Chimeric Antigen - therapeutic use ; United States</subject><ispartof>Clinical lymphoma, myeloma and leukemia, 2024-05, Vol.24 (5), p.316-322</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-acce8992f3485610df6a67743df0ea823410e00458163836b49e41796328e5a13</citedby><cites>FETCH-LOGICAL-c356t-acce8992f3485610df6a67743df0ea823410e00458163836b49e41796328e5a13</cites><orcidid>0000-0002-4052-7339 ; 0000-0003-0186-7987 ; 0000-0002-9609-6160</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38342727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shahzad, Moazzam</creatorcontrib><creatorcontrib>Khalid, Muhammad Fareed</creatorcontrib><creatorcontrib>Amin, Muhammad Kashif</creatorcontrib><creatorcontrib>Basharat, Ahmad</creatorcontrib><creatorcontrib>Ammad-Ud-Din, Mohammad</creatorcontrib><creatorcontrib>Park, Robin</creatorcontrib><creatorcontrib>Anwar, Iqra</creatorcontrib><creatorcontrib>Faisal, Muhammad Salman</creatorcontrib><creatorcontrib>Jaglal, Michael</creatorcontrib><title>Geographic and Racial Disparities in Chimeric Antigen Receptor–T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma</title><title>Clinical lymphoma, myeloma and leukemia</title><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><description>We investigate the geographical and racial disparities in accessing CAR-T and bispecific antibodies trials for DLBCL.
ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS version 26 was used for analysis.
There were 62 CAR-T and 13 bispecific antibodies trials with 6221 enrolled or expected to enroll patients. Eighty-five percent of the clinical trials were only open in the US, and the majority 64% were pharmaceutical-funded. There were 126 unique study sites distributed over 31 states with 11 (0-51) mean number of trials per state and 4.5 (1-26) and 4.4 (1-24) mean number of CAR-T and bispecific antibodies trials per site, respectively. Southern states had the most number of trials 31%, followed by Midwestern 25%, Northeastern 24%, and Western 20%. The highest number of study locations were in California 13, New York 9, and Pennsylvania 9, while the highest number of open studies were in California 51, Texas 32, and New York 23. Twenty states had no open CAR-T or bispecific antibodies trials. Only 33% of African Americans (AA) lived in a county with a trial, and 7 out of 10 states with the highest proportion of AA residents (18.6%-41.4%) have no or less than 4 trial sites. Of the 62 counties analyzed, 92% were White predominant, while only 8% were AA predominant (P = .009).
Strategies should be framed to address the observed disparities and to improve access.</description><subject>Antibodies, Bispecific - therapeutic use</subject><subject>CAR-T Cell</subject><subject>Clinical Trials</subject><subject>Clinical Trials as Topic</subject><subject>Geographical Disparities</subject><subject>Health Services Accessibility - statistics & numerical data</subject><subject>Healthcare Disparities - statistics & numerical data</subject><subject>Humans</subject><subject>Immunotherapy, Adoptive - methods</subject><subject>Lymphoma, Large B-Cell, Diffuse - immunology</subject><subject>Lymphoma, Large B-Cell, Diffuse - therapy</subject><subject>Receptors, Chimeric Antigen - immunology</subject><subject>Receptors, Chimeric Antigen - therapeutic use</subject><subject>United States</subject><issn>2152-2650</issn><issn>2152-2669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu1DAQhi1ERUvhBTggH7kkjB3HSSQu26UUpJUqVduz5XXGu14lcbCzlXrjGeAN-yQ43aVHTuPD93-a8U_IBwY5AyY_73PT9V3OgYscWA4gX5ELzkqecSmb1y_vEs7J2xj3ABUAa96Q86IuBK94dUF-36DfBj3unKF6aOmdNk539KuLow5uchipG-hy53oMCVkMk9viQO_Q4Dj58PTrz5ousevic_oqxdA4eyI3vp0F65CUkS6MwRip9SHprT1EpCsdtkivstlAV4_9uPO9fkfObOLx_Wlekvtv1-vl92x1e_NjuVhlpijllOmkq5uG20LUpWTQWqllVYmitYC65oVggACirJlM98qNaFCwqpEFr7HUrLgkn47eMfifB4yT6l00aRM9oD9ExRteiloIXiaUH1ETfIwBrRqD63V4VAzU3IXaq7kLNXehgKnURQp9PPkPmx7bl8i_z0_AlyOA6coHh0FF43Aw2LqAZlKtd__z_wWri5ss</recordid><startdate>202405</startdate><enddate>202405</enddate><creator>Shahzad, Moazzam</creator><creator>Khalid, Muhammad Fareed</creator><creator>Amin, Muhammad Kashif</creator><creator>Basharat, Ahmad</creator><creator>Ammad-Ud-Din, Mohammad</creator><creator>Park, Robin</creator><creator>Anwar, Iqra</creator><creator>Faisal, Muhammad Salman</creator><creator>Jaglal, Michael</creator><general>Elsevier 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>7X8</scope><orcidid>https://orcid.org/0000-0002-4052-7339</orcidid><orcidid>https://orcid.org/0000-0003-0186-7987</orcidid><orcidid>https://orcid.org/0000-0002-9609-6160</orcidid></search><sort><creationdate>202405</creationdate><title>Geographic and Racial Disparities in Chimeric Antigen Receptor–T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma</title><author>Shahzad, Moazzam ; Khalid, Muhammad Fareed ; Amin, Muhammad Kashif ; Basharat, Ahmad ; Ammad-Ud-Din, Mohammad ; Park, Robin ; Anwar, Iqra ; Faisal, Muhammad Salman ; Jaglal, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-acce8992f3485610df6a67743df0ea823410e00458163836b49e41796328e5a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibodies, Bispecific - therapeutic use</topic><topic>CAR-T Cell</topic><topic>Clinical Trials</topic><topic>Clinical Trials as Topic</topic><topic>Geographical Disparities</topic><topic>Health Services Accessibility - statistics & numerical data</topic><topic>Healthcare Disparities - statistics & numerical data</topic><topic>Humans</topic><topic>Immunotherapy, Adoptive - methods</topic><topic>Lymphoma, Large B-Cell, Diffuse - immunology</topic><topic>Lymphoma, Large B-Cell, Diffuse - therapy</topic><topic>Receptors, Chimeric Antigen - immunology</topic><topic>Receptors, Chimeric Antigen - therapeutic use</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shahzad, Moazzam</creatorcontrib><creatorcontrib>Khalid, Muhammad Fareed</creatorcontrib><creatorcontrib>Amin, Muhammad Kashif</creatorcontrib><creatorcontrib>Basharat, Ahmad</creatorcontrib><creatorcontrib>Ammad-Ud-Din, Mohammad</creatorcontrib><creatorcontrib>Park, Robin</creatorcontrib><creatorcontrib>Anwar, Iqra</creatorcontrib><creatorcontrib>Faisal, Muhammad Salman</creatorcontrib><creatorcontrib>Jaglal, Michael</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>Clinical lymphoma, myeloma and leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shahzad, Moazzam</au><au>Khalid, Muhammad Fareed</au><au>Amin, Muhammad Kashif</au><au>Basharat, Ahmad</au><au>Ammad-Ud-Din, Mohammad</au><au>Park, Robin</au><au>Anwar, Iqra</au><au>Faisal, Muhammad Salman</au><au>Jaglal, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Geographic and Racial Disparities in Chimeric Antigen Receptor–T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma</atitle><jtitle>Clinical lymphoma, myeloma and leukemia</jtitle><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><date>2024-05</date><risdate>2024</risdate><volume>24</volume><issue>5</issue><spage>316</spage><epage>322</epage><pages>316-322</pages><issn>2152-2650</issn><eissn>2152-2669</eissn><abstract>We investigate the geographical and racial disparities in accessing CAR-T and bispecific antibodies trials for DLBCL.
ClinicalTrials.gov was searched, and 75 trials with at least 1 open site in the US were included. 2020 US Census Bureau data was used to obtain data on race and ethnicity. SPSS version 26 was used for analysis.
There were 62 CAR-T and 13 bispecific antibodies trials with 6221 enrolled or expected to enroll patients. Eighty-five percent of the clinical trials were only open in the US, and the majority 64% were pharmaceutical-funded. There were 126 unique study sites distributed over 31 states with 11 (0-51) mean number of trials per state and 4.5 (1-26) and 4.4 (1-24) mean number of CAR-T and bispecific antibodies trials per site, respectively. Southern states had the most number of trials 31%, followed by Midwestern 25%, Northeastern 24%, and Western 20%. The highest number of study locations were in California 13, New York 9, and Pennsylvania 9, while the highest number of open studies were in California 51, Texas 32, and New York 23. Twenty states had no open CAR-T or bispecific antibodies trials. Only 33% of African Americans (AA) lived in a county with a trial, and 7 out of 10 states with the highest proportion of AA residents (18.6%-41.4%) have no or less than 4 trial sites. Of the 62 counties analyzed, 92% were White predominant, while only 8% were AA predominant (P = .009).
Strategies should be framed to address the observed disparities and to improve access.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38342727</pmid><doi>10.1016/j.clml.2024.01.006</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4052-7339</orcidid><orcidid>https://orcid.org/0000-0003-0186-7987</orcidid><orcidid>https://orcid.org/0000-0002-9609-6160</orcidid></addata></record> |
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subjects | Antibodies, Bispecific - therapeutic use CAR-T Cell Clinical Trials Clinical Trials as Topic Geographical Disparities Health Services Accessibility - statistics & numerical data Healthcare Disparities - statistics & numerical data Humans Immunotherapy, Adoptive - methods Lymphoma, Large B-Cell, Diffuse - immunology Lymphoma, Large B-Cell, Diffuse - therapy Receptors, Chimeric Antigen - immunology Receptors, Chimeric Antigen - therapeutic use United States |
title | Geographic and Racial Disparities in Chimeric Antigen Receptor–T Cells and Bispecific Antibodies Trials Access for Diffuse Large B-Cell Lymphoma |
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