Racial and ethnic disparities in a real-world precision oncology data registry

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作者
Alexander T. M. Cheung
Elina L. Palapattu
Isabella R. Pompa
Christopher M. Aldrighetti
Andrzej Niemierko
Henning Willers
Franklin Huang
Neha Vapiwala
Eliezer Van Allen
Sophia C. Kamran
机构
[1] NYU Grossman School of Medicine,Department of Radiation Oncology, Massachusetts General Hospital
[2] Broad Institute of Harvard and MIT,Division of Hematology/Oncology, Department of Medicine
[3] Dana-Farber Cancer Institute,Department of Radiation Oncology
[4] Harvard Medical School,undefined
[5] University of California,undefined
[6] San Francisco,undefined
[7] Hospital of the University of Pennsylvania,undefined
[8] Perelman School of Medicine,undefined
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Biorepositories enable precision oncology research by sharing clinically annotated genomic data, but it remains unknown whether these data registries reflect the true distribution of cancers in racial and ethnic minorities. Our analysis of Project Genomics Evidence Neoplasia Information Exchange (GENIE), a real-world cancer data registry designed to accelerate precision oncology discovery, indicates that minorities do not have sufficient representation, which may impact the validity of studies directly comparing mutational profiles between racial/ethnic groups and limit generalizability of biomarker discoveries to all populations.
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