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Patients carrying
by
Hayes, Daniel F
, Marcath, Lauren A
, Burness, Monika L
, Griggs, Jennifer J
, Henry, Norah Lynn
, Robinson, Adam C
, Poznak, Catherine Van
, Hertz, Daniel L
, Schott, Anne F
, Vangipuram, Kiran
, Kidwell, Kelley M
in
paclitaxel
/ pharmacogenomics
2018,2019
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Patients carrying
by
Hayes, Daniel F
, Marcath, Lauren A
, Burness, Monika L
, Griggs, Jennifer J
, Henry, Norah Lynn
, Robinson, Adam C
, Poznak, Catherine Van
, Hertz, Daniel L
, Schott, Anne F
, Vangipuram, Kiran
, Kidwell, Kelley M
in
paclitaxel
/ pharmacogenomics
2018,2019
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Journal Article
Patients carrying
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
Subject
MBRLCatalogueRelatedBooks
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