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Journal Article

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2018,2019
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Overview
First, evaluate if patients carrying putatively diminished activity genotype have longer paclitaxel exposure (e.g., time above threshold concentration of 0.05 μM [T ]). Second, screen additional pharmacogenes for associations with T . Pharmacogene panel genotypes were translated into genetic phenotypes for associations with T (n = 58). Patients with predicted low-activity CYP2C8 had shorter T after adjustment for age, body surface area and race (9.65 vs 11.03 hrs, β = 5.47, p = 0.02). This association was attributed to (p = 0.006), not (p = 0.58). Patients with predicted low-activity SLCO1B1 had longer T (12.12 vs 10.15 hrs, β = 0.85, p = 0.012). Contrary to previous publications, may confer increased paclitaxel metabolic activity. and genotype may explain some paclitaxel pharmacokinetic variability.
Publisher
Future Medicine Ltd

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