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Understanding inequities in precision oncology diagnostics
被引:0
|作者:
Ritika Dutta
Mounica Vallurupalli
Quinn McVeigh
Franklin W. Huang
Timothy R. Rebbeck
机构:
[1] Brigham and Women’s Hospital,Department of Medicine
[2] Harvard Medical School,Department of Medical Oncology
[3] Dana-Farber Cancer Institute,Cancer Program
[4] Broad Institute,Division of Hematology and Oncology, Department of Medicine
[5] University of California,undefined
[6] San Francisco,undefined
[7] Chan Zuckerberg Biohub,undefined
[8] San Francisco Veterans Health Care System,undefined
[9] Harvard TH Chan School of Public Health,undefined
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摘要:
Advances in molecular diagnostics have enabled the identification of targetable driver pathogenic variants, forming the basis of precision oncology care. However, the adoption of new technologies, such as next-generation sequencing (NGS) panels, can exacerbate healthcare disparities. Here, we summarize data on use patterns of advanced biomarker testing, highlight the disparities in both accessing NGS testing and using this data to match patients to appropriate personalized therapies and propose multidisciplinary strategies to address inequities looking forward.
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页码:787 / 794
页数:7
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