Pharmacogenetic Panel Testing: A Review of Current Practice and Potential for Clinical Implementation

被引:0
|
作者
Mosch, R. [1 ]
van der Lee, M. [1 ]
Guchelaar, H. J. [1 ]
Swen, J. J. [1 ]
机构
[1] Leiden Univ, Dept Clin Pharm & Toxicol, Med Ctr, Leiden, Netherlands
关键词
DIHYDROPYRIMIDINE DEHYDROGENASE GENOTYPE; CONSORTIUM CPIC GUIDELINE; FOR-MOLECULAR-PATHOLOGY; ADVERSE DRUG-REACTIONS; FLUOROPYRIMIDINE THERAPY; PRECISION MEDICINE; DECISION-SUPPORT; RANDOMIZED-TRIAL; RECOMMENDATIONS; ALLELE;
D O I
10.1146/annurev-pharmtox-061724-080935
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacogenetics (PGx) aims to optimize drug treatment outcomes by using a patient's genetic profile for individualized drug and dose selection. Currently, reactive and pretherapeutic single-gene PGx tests are increasingly applied in clinical practice in several countries and institutions. With over 95% of the population carrying at least one actionable PGx variant, and with drugs impacted by these genetic variants being in common use, pretherapeutic or preemptive PGx panel testing appears to be an attractive option for better-informed drug prescribing. Here, we discuss the current state of PGx panel testing and explore the potential for clinical implementation. We conclude that available evidence supports the implementation of pretherapeutic PGx panel testing for drugs covered in the PGx guidelines, yet identification of specific patient populations that benefit most and cost-effectiveness data are necessary to support large-scale implementation.
引用
收藏
页码:91 / 109
页数:19
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