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Missing diversity in brain tumor trials

BACKGROUND: Clinical trials for brain tumors represent a significant opportunity for both patients and providers to understand and combat a disease with substantial morbidity. The aim of this study was to quantify and map ethnic and racial representation in brain tumor trials and examine the potenti...

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Autores principales: Taha, Birra, Winston, Graham, Tosi, Umberto, Hartley, Benjamin, Hoffman, Caitlin, Dahmane, Nadia, Mason, Christopher E, Greenfield, Jeffrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316223/
https://www.ncbi.nlm.nih.gov/pubmed/32642711
http://dx.doi.org/10.1093/noajnl/vdaa059
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author Taha, Birra
Winston, Graham
Tosi, Umberto
Hartley, Benjamin
Hoffman, Caitlin
Dahmane, Nadia
Mason, Christopher E
Greenfield, Jeffrey P
author_facet Taha, Birra
Winston, Graham
Tosi, Umberto
Hartley, Benjamin
Hoffman, Caitlin
Dahmane, Nadia
Mason, Christopher E
Greenfield, Jeffrey P
author_sort Taha, Birra
collection PubMed
description BACKGROUND: Clinical trials for brain tumors represent a significant opportunity for both patients and providers to understand and combat a disease with substantial morbidity. The aim of this study was to quantify and map ethnic and racial representation in brain tumor trials and examine the potential gaps in trial recruitment. We also show that these representation gaps persist even in large multicultural cities like New York City. METHODS: We analyzed brain tumor clinical trials registered on www.clinicaltrials.gov between July 1, 2005 and completed on or before November 11, 2017. We used a combination of PubMed/MEDLINE and Google Scholar to find associated publications and obtained trial information as well as patient demographic information (when available) including race or ancestry. RESULTS: Out of 471 trials, 27% had no published results. Only 28.4% of trials with results reported race or ethnicity of trial participants, with no observed upward trend by year. Whites were significantly overrepresented in trials for metastatic brain tumors (P < .001) and high-grade trials (P < .001). Blacks/African Americans (AAs), Hispanics, and Asians were significantly underrepresented (P < .001) in high-grade trials, while only Blacks/AAs were underrepresented in trials for metastatic brain tumors (P < .001). Representation gaps were not observed in pediatric trials. Despite being a multicultural hub, New York City displayed similar gaps in trial representation. CONCLUSIONS: Despite increasing representation in the American population, minorities are underrepresented in brain tumor trials. In addition, despite numerous legal requirements and ethical mandates, published results including race-based information are remarkably absent from 70% of brain tumor trials.
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spelling pubmed-73162232020-07-07 Missing diversity in brain tumor trials Taha, Birra Winston, Graham Tosi, Umberto Hartley, Benjamin Hoffman, Caitlin Dahmane, Nadia Mason, Christopher E Greenfield, Jeffrey P Neurooncol Adv Clinical Investigations BACKGROUND: Clinical trials for brain tumors represent a significant opportunity for both patients and providers to understand and combat a disease with substantial morbidity. The aim of this study was to quantify and map ethnic and racial representation in brain tumor trials and examine the potential gaps in trial recruitment. We also show that these representation gaps persist even in large multicultural cities like New York City. METHODS: We analyzed brain tumor clinical trials registered on www.clinicaltrials.gov between July 1, 2005 and completed on or before November 11, 2017. We used a combination of PubMed/MEDLINE and Google Scholar to find associated publications and obtained trial information as well as patient demographic information (when available) including race or ancestry. RESULTS: Out of 471 trials, 27% had no published results. Only 28.4% of trials with results reported race or ethnicity of trial participants, with no observed upward trend by year. Whites were significantly overrepresented in trials for metastatic brain tumors (P < .001) and high-grade trials (P < .001). Blacks/African Americans (AAs), Hispanics, and Asians were significantly underrepresented (P < .001) in high-grade trials, while only Blacks/AAs were underrepresented in trials for metastatic brain tumors (P < .001). Representation gaps were not observed in pediatric trials. Despite being a multicultural hub, New York City displayed similar gaps in trial representation. CONCLUSIONS: Despite increasing representation in the American population, minorities are underrepresented in brain tumor trials. In addition, despite numerous legal requirements and ethical mandates, published results including race-based information are remarkably absent from 70% of brain tumor trials. Oxford University Press 2020-05-13 /pmc/articles/PMC7316223/ /pubmed/32642711 http://dx.doi.org/10.1093/noajnl/vdaa059 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Taha, Birra
Winston, Graham
Tosi, Umberto
Hartley, Benjamin
Hoffman, Caitlin
Dahmane, Nadia
Mason, Christopher E
Greenfield, Jeffrey P
Missing diversity in brain tumor trials
title Missing diversity in brain tumor trials
title_full Missing diversity in brain tumor trials
title_fullStr Missing diversity in brain tumor trials
title_full_unstemmed Missing diversity in brain tumor trials
title_short Missing diversity in brain tumor trials
title_sort missing diversity in brain tumor trials
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316223/
https://www.ncbi.nlm.nih.gov/pubmed/32642711
http://dx.doi.org/10.1093/noajnl/vdaa059
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