DPYD and UGT1A1 Pharmacogenetic Testing in Patients with Gastrointestinal Malignancies: An Overview of the Evidence and Considerations for Clinical Implementation. Issue 11 (19th October 2020)

• Record Type: Journal Article
• Authors: Varughese, Lisa A.; Lau‐Min, Kelsey S.; Cambareri, Christine; Damjanov, Nevena; Massa, Ryan; Reddy, Nandi; Oyer, Randall; Teitelbaum, Ursina; Tuteja, Sony
• Is Part Of: Pharmacotherapy. Volume 40:Issue 11(2020)
• Page Start: 1108
• Page End: 1129
• Publication Date: 2020-10-19
• Subjects: gastrointestinal neoplasms -- fluorouracil -- irinotecan -- drug‐related side effects -- adverse reactions -- pharmacogenetics -- pharmacogenomics -- toxicity -- implementation science -- pharmacology -- fluoropyrimidine; Chemotherapy -- Periodicals; Pharmacology -- Periodicals; Drug Therapy -- Periodicals; Pharmacology -- Periodicals; 615.1
• DOI: 10.1002/phar.2463
• Languages: English
• ISSNs: 0277-0008

Abstract

Abstract : Gastrointestinal (GI) malignancies are among the most commonly diagnosed cancers worldwide. Despite the introduction of targeted and immunotherapy agents in the treatment landscape, cytotoxic agents, such as fluoropyrimidines and irinotecan, remain as the cornerstone of chemotherapy for many of these tumors. Pharmacogenetics (PGx) is a rapidly evolving field that accounts for interpatient variability in drug metabolism to predict therapeutic response and toxicity. Given the significant incidence of severe treatment‐related adverse events associated with cytotoxic agents, utilizing PGx can allow clinicians to better anticipate drug tolerability while minimizing treatment interruptions or delays. In this review, the PGx profiles of drug‐gene pairs with potential impact in GI malignancy therapy – DPYD‐5‐fluorouracil/capecitabine and UGT1A1‐irinotecan – and the available clinical evidence of their roles in reducing severe adverse events are discussed. Considerations for clinical implementation, such as optimal laboratory workflows, electronic health record integration, and stakeholder engagement, as well as provider education, are addressed. Last, exploratory PGx markers in GI malignancy treatment are described. As the PGx knowledge base rapidly evolves, pharmacists will be vital in leveraging their pharmacology knowledge and clinical skills to implement PGx testing in the clinic.