Pharmacogenetics of Cancer Drugs

被引:38
作者
Hertz, Daniel L. [1 ]
Rae, James [2 ]
机构
[1] Univ Michigan, Coll Pharm, Dept Clin Social & Adm Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 66 | 2015年 / 66卷
关键词
germline genome; single-nucleotide polymorphism; THIOPURINE METHYLTRANSFERASE GENOTYPE; IMPLEMENTATION CONSORTIUM GUIDELINES; ACUTE LYMPHOBLASTIC-LEUKEMIA; RESPONSIVE BREAST-CANCER; DIHYDROPYRIMIDINE DEHYDROGENASE; CYP2D6; GENOTYPE; SEVERE TOXICITY; BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1; POSTMENOPAUSAL WOMEN; TAMOXIFEN RESPONSE;
D O I
10.1146/annurev-med-053013-053944
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The variability in treatment outcomes among patients receiving the same therapy for seemingly similar tumors can be attributed in part to genetics. The tumor's (somatic) genome largely dictates the effectiveness of the therapy, and the patient's (germline) genome influences drug exposure and the patient's sensitivity to toxicity. Many potentially clinically useful associations have been discovered between common germline genetic polymorphisms and outcomes of cancer treatment. This review highlights the germline pharmacogenetic associations that are currently being used to guide cancer treatment decisions, those that are most likely to someday be clinically useful, and associations that are well known but their roles in clinical management are not yet certain. In the future, germline genetic information will likely be available from tumor genetic analyses, creating an efficient opportunity to integrate the two genomes to optimize treatment outcomes for each individual cancer patient.
引用
收藏
页码:65 / 81
页数:17
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