Chimeric antigen receptor T cell therapy in oncology – Pipeline at a glance: Analysis of the ClinicalTrials.gov database
•We forecast 900 trials in CAR T-cell therapy during 2020–2025.•47 clinical trials use allogeneic products, and we expect this to double by 2025.•48 trials are using dual targeted CAR T-cells aiming to minimize antigen escape.•Phase 3 trials are registered for CD19, BCMA, CD123, and CLL1.•Anti-BCMA...
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Veröffentlicht in: | Critical reviews in oncology/hematology 2021-03, Vol.159, p.103239-103239, Article 103239 |
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creator | Moreno-Cortes, E. Forero-Forero, J.V. Lengerke-Diaz, P.A. Castro, J.E. |
description | •We forecast 900 trials in CAR T-cell therapy during 2020–2025.•47 clinical trials use allogeneic products, and we expect this to double by 2025.•48 trials are using dual targeted CAR T-cells aiming to minimize antigen escape.•Phase 3 trials are registered for CD19, BCMA, CD123, and CLL1.•Anti-BCMA CAR T-cell for multiple myeloma could be the next FDA approved product.
There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell therapy in oncology (cut-off December 2019). 593 trials were found.
48 % of trials are from China and 39 % from the USA. 63 % percent focused on hematologic malignancies, while gastrointestinal cancer, breast cancer, and nervous system were the top 3 solid tumors addressed. Common targets in hematologic malignancies are CD19 and BCMA; while mesothelin and CD171 in solid tumors. Second-generation CAR T designs predominate with CD28 or 41BB co-stimulation. Mixed sponsors supported 45 % of trials, and only 19 % received funding exclusively from industry.
Current trends suggest that 900 CAR T-cell therapy clinical trials will be registered during 2020–2025. We estimate a two-fold increase in trials that study allogeneic cell products in the next five years. |
doi_str_mv | 10.1016/j.critrevonc.2021.103239 |
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There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell therapy in oncology (cut-off December 2019). 593 trials were found.
48 % of trials are from China and 39 % from the USA. 63 % percent focused on hematologic malignancies, while gastrointestinal cancer, breast cancer, and nervous system were the top 3 solid tumors addressed. Common targets in hematologic malignancies are CD19 and BCMA; while mesothelin and CD171 in solid tumors. Second-generation CAR T designs predominate with CD28 or 41BB co-stimulation. Mixed sponsors supported 45 % of trials, and only 19 % received funding exclusively from industry.
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There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell therapy in oncology (cut-off December 2019). 593 trials were found.
48 % of trials are from China and 39 % from the USA. 63 % percent focused on hematologic malignancies, while gastrointestinal cancer, breast cancer, and nervous system were the top 3 solid tumors addressed. Common targets in hematologic malignancies are CD19 and BCMA; while mesothelin and CD171 in solid tumors. Second-generation CAR T designs predominate with CD28 or 41BB co-stimulation. Mixed sponsors supported 45 % of trials, and only 19 % received funding exclusively from industry.
Current trends suggest that 900 CAR T-cell therapy clinical trials will be registered during 2020–2025. We estimate a two-fold increase in trials that study allogeneic cell products in the next five years.</description><subject>Adoptive immunotherapy</subject><subject>Antigens, CD19</subject><subject>Cell- and Tissue-Based Therapy</subject><subject>Chimeric antigen receptor</subject><subject>Clinical Trials as Topic</subject><subject>Databases, Factual</subject><subject>Humans</subject><subject>Immunotherapy, Adoptive</subject><subject>Neoplasm antigens</subject><subject>Neoplasms - therapy</subject><subject>Receptors, Antigen, T-Cell - genetics</subject><subject>Receptors, Chimeric Antigen - genetics</subject><subject>Trends</subject><issn>1040-8428</issn><issn>1879-0461</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM-O0zAQhy0EYpeFV0Bz5JJiO46dcFsq_kkrwaGcrYkz6bpK42C7lcqJd-ANeRJcdYEjJ49G388_zccYCL4SXOjXu5WLPkc6htmtJJeirGtZd4_YtWhNV3GlxeMyc8WrVsn2ij1Lacc5V0qbp-yqrlVnjObX7Pv63u8pegc4Z7-lGSI5WnKIsAFH0wT5niIuJ_AzlLYwhe0Jfv34CV_8QpOfCTADwnbC2dEbuJ1xOiWfIIznJKwL4h1Om-hxSqttOMKAGXtM9Jw9GcuOXjy8N-zr-3eb9cfq7vOHT-vbu8rVRuUKOTdI2GvukDrBNW9GoZXEoe8Go6keyWDnhqZBI8ZOSyO7RvR9TX2rVNPXN-zV5d8lhm8HStnufTqfhjOFQ7JStUI3RmlZ0PaCuhhSijTaJfo9xpMV3J7N2539Z96ezduL-RJ9-dBy6Pc0_A3-UV2AtxeAyq1HT9Em56lIG3xRnu0Q_P9bfgMv95wg</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>Moreno-Cortes, E.</creator><creator>Forero-Forero, J.V.</creator><creator>Lengerke-Diaz, P.A.</creator><creator>Castro, J.E.</creator><general>Elsevier B.V</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/0000-0002-1285-8499</orcidid><orcidid>https://orcid.org/0000-0001-7629-6264</orcidid><orcidid>https://orcid.org/0000-0001-9872-5760</orcidid></search><sort><creationdate>202103</creationdate><title>Chimeric antigen receptor T cell therapy in oncology – Pipeline at a glance: Analysis of the ClinicalTrials.gov database</title><author>Moreno-Cortes, E. ; Forero-Forero, J.V. ; Lengerke-Diaz, P.A. ; Castro, J.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c374t-a007aeab60cae910605f1642adb9d76e3fe7a9cd55a71f96272951bb3eb8445b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adoptive immunotherapy</topic><topic>Antigens, CD19</topic><topic>Cell- and Tissue-Based Therapy</topic><topic>Chimeric antigen receptor</topic><topic>Clinical Trials as Topic</topic><topic>Databases, Factual</topic><topic>Humans</topic><topic>Immunotherapy, Adoptive</topic><topic>Neoplasm antigens</topic><topic>Neoplasms - therapy</topic><topic>Receptors, Antigen, T-Cell - genetics</topic><topic>Receptors, Chimeric Antigen - genetics</topic><topic>Trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moreno-Cortes, E.</creatorcontrib><creatorcontrib>Forero-Forero, J.V.</creatorcontrib><creatorcontrib>Lengerke-Diaz, P.A.</creatorcontrib><creatorcontrib>Castro, J.E.</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>Critical reviews in oncology/hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno-Cortes, E.</au><au>Forero-Forero, J.V.</au><au>Lengerke-Diaz, P.A.</au><au>Castro, J.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chimeric antigen receptor T cell therapy in oncology – Pipeline at a glance: Analysis of the ClinicalTrials.gov database</atitle><jtitle>Critical reviews in oncology/hematology</jtitle><addtitle>Crit Rev Oncol Hematol</addtitle><date>2021-03</date><risdate>2021</risdate><volume>159</volume><spage>103239</spage><epage>103239</epage><pages>103239-103239</pages><artnum>103239</artnum><issn>1040-8428</issn><eissn>1879-0461</eissn><abstract>•We forecast 900 trials in CAR T-cell therapy during 2020–2025.•47 clinical trials use allogeneic products, and we expect this to double by 2025.•48 trials are using dual targeted CAR T-cells aiming to minimize antigen escape.•Phase 3 trials are registered for CD19, BCMA, CD123, and CLL1.•Anti-BCMA CAR T-cell for multiple myeloma could be the next FDA approved product.
There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell therapy in oncology (cut-off December 2019). 593 trials were found.
48 % of trials are from China and 39 % from the USA. 63 % percent focused on hematologic malignancies, while gastrointestinal cancer, breast cancer, and nervous system were the top 3 solid tumors addressed. Common targets in hematologic malignancies are CD19 and BCMA; while mesothelin and CD171 in solid tumors. Second-generation CAR T designs predominate with CD28 or 41BB co-stimulation. Mixed sponsors supported 45 % of trials, and only 19 % received funding exclusively from industry.
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subjects | Adoptive immunotherapy Antigens, CD19 Cell- and Tissue-Based Therapy Chimeric antigen receptor Clinical Trials as Topic Databases, Factual Humans Immunotherapy, Adoptive Neoplasm antigens Neoplasms - therapy Receptors, Antigen, T-Cell - genetics Receptors, Chimeric Antigen - genetics Trends |
title | Chimeric antigen receptor T cell therapy in oncology – Pipeline at a glance: Analysis of the ClinicalTrials.gov database |
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