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.
机构:
Washington Univ, Sch Med, McDonnell Genome Inst, St Louis, MO 63110 USA
Washington Univ, Sch Med, Div Oncol, Dept Internal Med, St Louis, MO 63110 USAWashington Univ, Sch Med, McDonnell Genome Inst, St Louis, MO 63110 USA
Dang, Ha X.
Maher, Christopher A.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, McDonnell Genome Inst, St Louis, MO 63110 USA
Washington Univ, Sch Med, Div Oncol, Dept Internal Med, St Louis, MO 63110 USA
Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
Washington Univ, Sch Med, Dept Biomed Engn, St Louis, MO 63110 USAWashington Univ, Sch Med, McDonnell Genome Inst, St Louis, MO 63110 USA