Abstract
Precision medicine has revolutionized clinical care for patients with cancer through the development of targeted therapy, identification of inherited cancer predisposition syndromes and the use of pharmacogenetics to optimize pharmacotherapy for anticancer drugs and supportive care medications. While germline (patient) and somatic (tumor) genomic testing have evolved separately, recent interest in paired germline/somatic testing has led to an increase in integrated genomic testing workflows. However, paired germline/somatic testing has generally lacked the incorporation of germline pharmacogenomics. Integrating pharmacogenomics into paired germline/somatic genomic testing would be an efficient method for increasing access to pharmacogenomic testing. In this perspective, the authors argue for the benefits of implementing a comprehensive approach integrating somatic and germline testing that is inclusive of pharmacogenomics in clinical practice. Tweetable abstract In this perspective, the authors argue that integrating pharmacogenomic testing into paired germline/somatic genomic testing would be an efficient method for increasing access to pharmacogenomic testing.
Original language | English |
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Pages (from-to) | 731-738 |
Number of pages | 8 |
Journal | Pharmacogenomics |
Volume | 24 |
Issue number | 13 |
DOIs | |
State | Published - Aug 1 2023 |
Bibliographical note
Publisher Copyright:© 2023 Future Medicine Ltd.
Funding
AA Salahudeen reports employment by Tempus Labs Inc. JM Kolesar reports ownership in Helix Diagnostics and grant support by ArtemiLife and LOXO@Lilly. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. Financial & competing interests disclosure AA Salahudeen reports employment by Tempus Labs Inc. JM Kolesar reports ownership in Helix Diagnostics and grant support by ArtemiLife and LOXO@Lilly. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
Funders | Funder number |
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ArtemiLife Incorporated | |
Tempus Labs Inc |
Keywords
- PGx
- adverse events
- cancer
- malignancy
- precision medicine
ASJC Scopus subject areas
- Molecular Medicine
- Genetics
- Pharmacology