Drug development in the era of precision medicine

被引:275
|
作者
Dugger, Sarah A. [1 ,2 ]
Platt, Adam [3 ]
Goldstein, David B. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Med Ctr, Hammer Hlth Sci, Inst Genom Med, 1408,701 West 168th St, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Hammer Hlth Sci, Dept Genet & Dev Columbia, 701 West 168th St, New York, NY 10032 USA
[3] AstraZeneca, AstraZeneca Ctr Genom Res Precis Med & Genom, IMED Biotech Unit, 1 Francis Crick Ave,Cambridge Biomed Campus, Cambridge CB2 0AA, England
关键词
CELL LUNG-CANCER; GENOME-WIDE ASSOCIATION; DE-NOVO MUTATIONS; OPEN-LABEL; PHASE-III; 1ST-LINE TREATMENT; DOUBLE-BLIND; NUCLEOTIDE POLYMORPHISM; POSTMENOPAUSAL WOMEN; MAINTENANCE THERAPY;
D O I
10.1038/nrd.2017.226
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
For the past three decades, the use of genomics to inform drug discovery and development pipelines has generated both excitement and scepticism. Although earlier efforts successfully identified some new drug targets, the overall clinical efficacy of developed drugs has remained unimpressive, owing in large part to the heterogeneous causes of disease. Recent technological and analytical advances in genomics, however, have now made it possible to rapidly identify and interpret the genetic variation underlying a single patient's disease, thereby providing a window into patient-specific mechanisms that cause or contribute to disease, which could ultimately enable the 'precise' targeting of these mechanisms. Here, we first examine and highlight the successes and limitations of the earlier phases of genomics in drug discovery and development. We then review the current major efforts in precision medicine and discuss the potential broader utility of mechanistically guided treatments going forward.
引用
收藏
页码:183 / 196
页数:14
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