Table 1:
Drug | Major lessons learned |
---|---|
Warfarin | • Define multiple genetic pathways and specific variants modulating drug action prior to mounting trials • Include multiple ancestries • Specific endpoints chosen (e.g. efficacy versus adverse events) determine ability to detect an effect |
Abacavir, carbamazepine | • Pre-clinical data may align with RCT outcomes • Endpoints should be defined as precisely as possible • Practitioner education is critical to successful implementation • Include multiple ancestries |
Clopidogrel | • Include multiple ancestries • Variant allele frequency determine the likelihood of defining a pharmacogenetic outcome effect |
Azathioprine | • A potentially beneficial outcome of pharmacogenetic testing is confined to patients with variant alleles • Equipoise can change as genotypes become available and used |