Abstract
Pharmacogenomics has the potential to not only impact the pharmacokinetics of an anticancer drug but also the tumor response, or pharmacodynamics. This chapter focuses on the most up-to-date clinical trials involving pharmacogenomics and anticancer therapy. A brief introduction of drug development and the difference between somatic and germline DNA mutations sets up the chapter for understanding the progress which has been made in regard to individualized cancer therapy. Although researchers and healthcare practitioners have realized the potential of pharmacogenomics for several years, it has only been until recently that genotype-guided, prospective clinical trials have been done. Validating these biomarkers and genetic associations is vital to translating pharmacogenomics into clinical practice. This chapter highlights the advancements that have been made with key examples such as tamoxifen and CYP2D6, erlotinib and EGFR, vemurafenib and BRAF, and many others.
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Patel, J.N., McLeod, H.L. (2014). Pharmacogenomics and Cancer Therapy: Somatic and Germline Polymorphisms. In: Rudek, M., Chau, C., Figg, W., McLeod, H. (eds) Handbook of Anticancer Pharmacokinetics and Pharmacodynamics. Cancer Drug Discovery and Development. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-9135-4_15
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