Using Germline Genomics to Individualize Pediatric Cancer Treatments

被引:13
作者
Pinto, Navin [1 ,3 ]
Cohn, Susan L. [1 ,3 ]
Dolan, M. Eileen [2 ,3 ]
机构
[1] Univ Chicago, Dept Pediat, KCBD, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[3] Univ Chicago, Comm Clin Pharmacol & Pharmacogenom, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; THIOPURINE S-METHYLTRANSFERASE; INOSINE-TRIPHOSPHATE-PYROPHOSPHATASE; PHARMACOGENOMIC DISCOVERY; MERCAPTOPURINE METABOLISM; CISPLATIN OTOTOXICITY; GENETIC-POLYMORPHISM; ETHNIC-DIFFERENCES; HEARING-LOSS; CELL-LINES;
D O I
10.1158/1078-0432.CCR-11-1938
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The amazing successes in cure rates for children with cancer over the last century have come in large part from identifying clinical, genetic, and molecular variables associated with response to therapy in large cooperative clinical trials and stratifying therapies according to the predicted risk of relapse. There is an expanding interest in identifying germline genomic variants, as opposed to genetic variants within the tumor, that are associated with susceptibility to toxicity and for risk of relapse. This review highlights the most important germline pharmacogenetic and pharmacogenomic studies in pediatric oncology. Incorporating germline genomics into risk-adapted therapies will likely lead to safer and more effective treatments for children with cancer. Clin Cancer Res; 18(10); 2791-800. (C)2012 AACR.
引用
收藏
页码:2791 / 2800
页数:10
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