4.6 Review

Moving Pharmacogenetics Into Practice: It's All About the Evidence!

Journal

CLINICAL PHARMACOLOGY & THERAPEUTICS
Volume 110, Issue 3, Pages 649-661

Publisher

WILEY
DOI: 10.1002/cpt.2327

Keywords

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Funding

  1. NIH K08 award from NHLBI [K08 HL146990]
  2. NIH [U01 HG007269, UL1 TR001427, R01 HL149752, U01 HG010232]
  3. Burroughs Wellcome Fund Innovation in Regulatory Science Award [1015006]
  4. NCATS/NIH [UL1 TR000445]

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The evidence for pharmacogenetics is growing rapidly, but the strength of evidence required for clinical implementation is debated. This review summarizes different perspectives on the evidence needed for clinical implementation, including patient cases, resources, types of evidence, limitations, implementers, clinicians, and patients' perspectives, as well as future perspectives and the need for education. Standardization efforts are underway, with recognition of the value of pharmacogenetic testing from the patient perspective, and the need for consideration of multiple stakeholder perspectives, particularly that of the patient.
The evidence for pharmacogenetics has grown rapidly in recent decades. However, the strength of evidence required for the clinical implementation of pharmacogenetics is highly debated. Therefore, the purpose of this review is to summarize different perspectives on the evidence required for the clinical implementation of pharmacogenetics. First, we present two patient cases that demonstrate how knowledge of pharmacogenetic evidence affected their care. Then we summarize resources that curate pharmacogenetic evidence, types of evidence (with an emphasis on randomized controlled trials [RCT]) and their limitations, and different perspectives from implementers, clinicians, and patients. We compare pharmacogenetics to a historical example (i.e., the evidence required for the clinical implementation of pharmacokinetics/therapeutic drug monitoring), and we provide future perspectives on the evidence for pharmacogenetic panels and the need for more education in addition to evidence. Although there are differences in the interpretation of pharmacogenetic evidence across resources, efforts for standardization are underway. Survey data illustrate the value of pharmacogenetic testing from the patient perspective, with their providers seen as key to ensuring maximum benefit from test results. However, clinicians and practice guidelines from medical societies often rely on RCT data to guide treatment decisions, which are not always feasible or ethical in pharmacogenetics. Thus, recognition of other types of evidence to support pharmacogenetic implementation is needed. Among pharmacogenetic implementers, consistent evidence of pharmacogenetic associations is deemed most critical. Ultimately, moving pharmacogenetics into practice will require consideration of multiple stakeholder perspectives, keeping particularly attuned to the voice of the ultimate stakeholder-the patient.

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