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  4. Analysis of Racial/Ethnic Representation in Select Basic and Applied Cancer Research Studies
 
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Analysis of Racial/Ethnic Representation in Select Basic and Applied Cancer Research Studies

Journal
Scientific Reports
ISSN
2045-2322
Date Issued
2018-09-18
Author(s)
Santiago Guerrero
Andrés López-Cortés
Alberto Indacochea
Jennyfer M. García-Cárdenas
Facultad de Ciencias de la Salud Eugenio Espejo  
ZAMBRANO ESPINOSA, ANA KARINA  
Facultad de Ciencias de la Salud Eugenio Espejo  
Alejandro Cabrera-Andrade
Facultad de Ciencias de la Salud Eugenio Espejo  
GUEVARA RAMIREZ, ALEXANDRA PATRICIA  
Facultad de Ciencias de la Salud Eugenio Espejo  
Diana Abigail González
Facultad de Ciencias de la Salud Eugenio Espejo  
Paola E. Leone
Facultad de Ciencias de la Salud Eugenio Espejo  
PAZ Y MIÑO CEPEDA, CESAR ANTONIO  
Facultad de Ciencias de la Salud Eugenio Espejo  
DOI
10.1038/s41598-018-32264-x
Abstract
<jats:title>Abstract</jats:title><jats:p>Over the past decades, consistent studies have shown that race/ethnicity have a great impact on cancer incidence, survival, drug response, molecular pathways and epigenetics. Despite the influence of race/ethnicity in cancer outcomes and its impact in health care quality, a comprehensive understanding of racial/ethnic inclusion in oncological research has never been addressed. We therefore explored the racial/ethnic composition of samples/individuals included in fundamental (patient-derived oncological models, biobanks and genomics) and applied cancer research studies (clinical trials). Regarding patient-derived oncological models (n = 794), 48.3% have no records on their donor’s race/ethnicity, the rest were isolated from White (37.5%), Asian (10%), African American (3.8%) and Hispanic (0.4%) donors. Biobanks (n = 8,293) hold specimens from unknown (24.56%), White (59.03%), African American (11.05%), Asian (4.12%) and other individuals (1.24%). Genomic projects (n = 6,765,447) include samples from unknown (0.6%), White (91.1%), Asian (5.6%), African American (1.7%), Hispanic (0.5%) and other populations (0.5%). Concerning clinical trials (n = 89,212), no racial/ethnic registries were found in 66.95% of participants, and records were mainly obtained from Whites (25.94%), Asians (4.97%), African Americans (1.08%), Hispanics (0.16%) and other minorities (0.9%). Thus, two tendencies were observed across oncological studies: lack of racial/ethnic information and overrepresentation of Caucasian/White samples/individuals. These results clearly indicate a need to diversify oncological studies to other populations along with novel strategies to enhanced race/ethnicity data recording and reporting.</jats:p>

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