Precision oncology: lessons learned and challenges for the future

被引:9
|
作者
Yang, Hsih-Te [1 ]
Shah, Ronak H. [1 ,2 ]
Tegay, David [1 ]
Onel, Kenan [3 ]
机构
[1] Northwell Hlth, Dept Pediat, Med Genet & Human Genom, New York, NY USA
[2] Northwell Hlth, Ctr Res Informat & Innovat, Feinstein Inst Med Res, New York, NY USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, 1 Gustave L Levy Pl,Box 1498, New York, NY 10029 USA
来源
关键词
next-generation sequencing; pathogenic variant; driver mutation; actionable mutation; cancer disparities; PROOF-OF-CONCEPT; MUTATIONAL PROCESSES; CLINICAL INTERPRETATION; CONVENTIONAL THERAPY; GENOMIC LANDSCAPE; MEDICAL GENETICS; PEDIATRIC CANCER; AMERICAN-COLLEGE; BREAST-CANCER; HIGH-RISK;
D O I
10.2147/CMAR.S201326
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The decreasing cost of and increasing capacity of DNA sequencing has led to vastly increased opportunities for population-level genomic studies to discover novel genomic alterations associated with both Mendelian and complex phenotypes. To translate genomic findings clinically, a number of health care institutions have worked collaboratively or individually to initiate precision medicine programs. These precision medicine programs involve designing patient enrollment systems, tracking electronic health records, building biobank repositories, and returning results with actionable matched therapies. As cancer is a paradigm for genetic diseases and new therapies are increasingly tailored to attack genetic susceptibilities in tumors, these precision medicine programs are largely driven by the urgent need to perform genetic profiling on cancer patients in real time. Here, we review the current landscape of precision oncology and highlight challenges to be overcome and examples of benefits to patients. Furthermore, we make suggestions to optimize future precision oncology programs based upon the lessons learned from these "first generation" early adopters.
引用
收藏
页码:7525 / 7536
页数:12
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