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Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms

IMPORTANCE: Disparities that affect Black persons with various hematological malignant neoplasms are substantial, yet little is known about disparities related to the use of US Food and Drug Administration (FDA)–approved chimeric antigen receptor–T cell (CAR-T) therapy. OBJECTIVE: To examine the enr...

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Autores principales: Al Hadidi, Samer, Schinke, Carolina, Thanendrarajan, Sharmilan, Zangari, Maurizio, van Rhee, Frits
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021907/
https://www.ncbi.nlm.nih.gov/pubmed/35442451
http://dx.doi.org/10.1001/jamanetworkopen.2022.8161
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author Al Hadidi, Samer
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
van Rhee, Frits
author_facet Al Hadidi, Samer
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
van Rhee, Frits
author_sort Al Hadidi, Samer
collection PubMed
description IMPORTANCE: Disparities that affect Black persons with various hematological malignant neoplasms are substantial, yet little is known about disparities related to the use of US Food and Drug Administration (FDA)–approved chimeric antigen receptor–T cell (CAR-T) therapy. OBJECTIVE: To examine the enrollment of Black participants in clinical trials that resulted in a subsequent FDA approval of CAR-T products in hematological malignant neoplasms. DESIGN, SETTING, AND PARTICIPANTS: A cross-sectional study was performed using publicly available data on drug products and demographic subgroups from Drugs@fda in the period of August 2017 to May 2021. Data analysis included patients with large B cell lymphoma, follicular lymphoma, mantle cell lymphoma, acute lymphoblastic leukemia, and multiple myeloma who were enrolled into 7 clinical trials that investigated various CAR-T products. The study was conducted from July 1, 2021, to November 30, 2021. MAIN OUTCOMES AND MEASURES: Frequencies of participation of Black participants were calculated with adjustment for disease prevalence. RESULTS: Of the 1057 enrolled patients included in the study, CAR-T products were given to 746 patients (71%), and efficacy was reported for 729 enrolled patients (69%) across all the approved CAR-T products and indications. Most patients (1015 patients [96%]) were enrolled in the US. Black participants were included in the racial category other in the study that supported tisagenlecleucel approval in acute lymphoblastic leukemia; otherwise, their enrollment was specified either in the study publication and/or the demographic subgroup information available under the FDA product labeling information. The number of Black participants who received the CAR-T product and had reported efficacy varied between studies (range, 1-12 participants [2%-5%]). Adjusted prevalence measures showed the lowest participation to prevalence ratio of 0.2 for multiple myeloma and 0.6 for large B cell lymphoma. CONCLUSIONS AND RELEVANCE: The findings of this study suggest that there are substantial disparities affecting Black patients across all approved CAR-T products used to treat hematological malignant neoplasms with otherwise limited effective treatment options. The study findings might aid policy discussions regarding the immediate need of regulations that enforce certain thresholds of Black patients’ enrollment before granting FDA approval.
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spelling pubmed-90219072022-05-02 Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms Al Hadidi, Samer Schinke, Carolina Thanendrarajan, Sharmilan Zangari, Maurizio van Rhee, Frits JAMA Netw Open Original Investigation IMPORTANCE: Disparities that affect Black persons with various hematological malignant neoplasms are substantial, yet little is known about disparities related to the use of US Food and Drug Administration (FDA)–approved chimeric antigen receptor–T cell (CAR-T) therapy. OBJECTIVE: To examine the enrollment of Black participants in clinical trials that resulted in a subsequent FDA approval of CAR-T products in hematological malignant neoplasms. DESIGN, SETTING, AND PARTICIPANTS: A cross-sectional study was performed using publicly available data on drug products and demographic subgroups from Drugs@fda in the period of August 2017 to May 2021. Data analysis included patients with large B cell lymphoma, follicular lymphoma, mantle cell lymphoma, acute lymphoblastic leukemia, and multiple myeloma who were enrolled into 7 clinical trials that investigated various CAR-T products. The study was conducted from July 1, 2021, to November 30, 2021. MAIN OUTCOMES AND MEASURES: Frequencies of participation of Black participants were calculated with adjustment for disease prevalence. RESULTS: Of the 1057 enrolled patients included in the study, CAR-T products were given to 746 patients (71%), and efficacy was reported for 729 enrolled patients (69%) across all the approved CAR-T products and indications. Most patients (1015 patients [96%]) were enrolled in the US. Black participants were included in the racial category other in the study that supported tisagenlecleucel approval in acute lymphoblastic leukemia; otherwise, their enrollment was specified either in the study publication and/or the demographic subgroup information available under the FDA product labeling information. The number of Black participants who received the CAR-T product and had reported efficacy varied between studies (range, 1-12 participants [2%-5%]). Adjusted prevalence measures showed the lowest participation to prevalence ratio of 0.2 for multiple myeloma and 0.6 for large B cell lymphoma. CONCLUSIONS AND RELEVANCE: The findings of this study suggest that there are substantial disparities affecting Black patients across all approved CAR-T products used to treat hematological malignant neoplasms with otherwise limited effective treatment options. The study findings might aid policy discussions regarding the immediate need of regulations that enforce certain thresholds of Black patients’ enrollment before granting FDA approval. American Medical Association 2022-04-20 /pmc/articles/PMC9021907/ /pubmed/35442451 http://dx.doi.org/10.1001/jamanetworkopen.2022.8161 Text en Copyright 2022 Al Hadidi S et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Al Hadidi, Samer
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
van Rhee, Frits
Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title_full Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title_fullStr Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title_full_unstemmed Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title_short Enrollment of Black Participants in Pivotal Clinical Trials Supporting US Food and Drug Administration Approval of Chimeric Antigen Receptor–T Cell Therapy for Hematological Malignant Neoplasms
title_sort enrollment of black participants in pivotal clinical trials supporting us food and drug administration approval of chimeric antigen receptor–t cell therapy for hematological malignant neoplasms
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021907/
https://www.ncbi.nlm.nih.gov/pubmed/35442451
http://dx.doi.org/10.1001/jamanetworkopen.2022.8161
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