Members of our team had the opportunity to present a new poster abstract, "Implementing a Health-System Specialty Pharmacist-Led Pharmacogenomic Protocol for DPYD Genetic Testing to Optimize Capecitabine Safety", at the NASP 2025 Annual Meeting & Expo.
Authors:
Diana Nguyen, PharmD; Andrew Wash, PharmD, PhD; Ana Lopez Medina, PharmD, PhD; Casey Fitzpatrick, PharmD; Abbey Hunter, PharmD, CSP; Katie Jo Cash, PharmD, CSP; Kristin Hutchinson, PharmD, CSP; Jessica Mourani, PharmD
Background:
Objectives:
Read about the team's findings by downloading the outcomes study below.
1 De Mattia E, Silvestri M, Polesel J, et al. Rare genetic variant burden in DPYD predicts severe fluoropyrimidine- related toxicity risk. BiomedPharmacother. 2022;154:113644. doi:10.1016/j.biopha.2022.113644
2 Chenchula S, Atal S, Uppugunduri CRS. A review of real-world evidence on preemptive pharmacogenomic testing for preventing adverse drug reactions: a reality for future health care. Pharmacogenomics J . 2024;24(2):9. doi:10.1038/s41397-024-00326-l
3 Virelli CR, Mohiuddin AG, Kennedy JL. Barriers to clinical adoption of pharmacogenomic testing in psychiatry: a critical analysis. Transl Psychiatry. 2021 Oct 6;11(1):509. doi: 10.1038/s41398-021-01600-7. PMID: 34615849; PMCID: PMC8492820.