Recommendations for pharmacogenetic testing in clinical practice guidelines in the US

被引:1
|
作者
Hertz, Daniel L. [1 ]
Bousman, Chad A. [2 ]
McLeod, Howard L. [3 ]
Monte, Andrew A. [4 ]
Voora, Deepak [5 ]
Orlando, Lori A. [6 ]
Crutchley, Rustin D. [7 ]
Brown, Benjamin [8 ]
Teeple, Wrenda [9 ]
Rogers, Sara [10 ]
Patel, Jai N. [11 ,12 ]
机构
[1] Univ Michigan, Coll Pharm, Dept Clin Pharm, Ann Arbor, MI 48109 USA
[2] Univ Calgary, Dept Med Genet, Calgary, AB, Canada
[3] Utah Tech Univ, Ctr Precis Med & Funct Genom, St George, UT USA
[4] Univ Colorado, Sch Med, Dept Emergency Med, Sect Pharmacol & Med Toxicol, Aurora, CO USA
[5] Duke Univ, Dept Med, Duke Precis Med Program, Durham, NC USA
[6] Duke Univ, Dept Med, Durham, NC USA
[7] Univ Manchester, Coll Pharm, Dept Pharmaceut Sci, Ft Wayne, IN USA
[8] Amer Soc Pharmacovigilance, Houston, TX USA
[9] Arbit Consulting LLC, Minneapolis, MN USA
[10] Amer Soc Pharmacovigilance, Bryan, TX USA
[11] Atrium Hlth, Levine Canc Inst, Dept Canc Pharmacol & Pharmacogen, Winston Salem, NC USA
[12] Atrium Hlth Wake Forest Baptist Comprehens Canc Ct, Winston Salem, NC USA
关键词
clinical practice guidelines; clinical utility; genetic testing; pharmacogenetic testing; pharmacogenomics; INFECTIOUS-DISEASES-SOCIETY; ASSOCIATION TASK-FORCE; PERCUTANEOUS CORONARY INTERVENTION; ELEVATION MYOCARDIAL-INFARCTION; 2011 ACCF/AHA/SCAI GUIDELINE; MAJOR DEPRESSIVE DISORDER; AMERICAN-COLLEGE; SYSTEMIC THERAPY; FOCUSED UPDATE; MANAGEMENT;
D O I
10.1093/ajhp/zxae110
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose Pharmacogenetic testing can identify patients who may benefit from personalized drug treatment. However, clinical uptake of pharmacogenetic testing has been limited. Clinical practice guidelines recommend biomarker tests that the guideline authors deem to have demonstrated clinical utility, meaning that testing improves treatment outcomes. The objective of this narrative review is to describe the current status of pharmacogenetic testing recommendations within clinical practice guidelines in the US.Summary Guidelines were reviewed for pharmacogenetic testing recommendations for 21 gene-drug pairs that have well-established drug response associations and all of which are categorized as clinically actionable by the Clinical Pharmacogenetics Implementation Consortium. The degree of consistency within and between organizations in pharmacogenetic testing recommendations was assessed. Relatively few clinical practice guidelines that provide a pharmacogenetic testing recommendation were identified. Testing recommendations for HLA-B*57:01 before initiation of abacavir and G6PD before initiation of rasburicase, both of which are included in drug labeling, were mostly consistent across guidelines. Gene-drug pairs with at least one clinical practice guideline recommending testing or stating that testing could be considered included CYP2C19-clopidogrel, CYP2D6-codeine, CYP2D6-tramadol, CYP2B6-efavirenz, TPMT-thiopurines, and NUDT15-thiopurines. Testing recommendations for the same gene-drug pair were often inconsistent between organizations and sometimes inconsistent between different guidelines from the same organization.Conclusion A standardized approach to evaluating the evidence of clinical utility for pharmacogenetic testing may increase the inclusion and consistency of pharmacogenetic testing recommendations in clinical practice guidelines, which could benefit patients and society by increasing clinical use of pharmacogenetic testing.
引用
收藏
页码:672 / 683
页数:12
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