<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Thompson P</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>831-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4282931</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(4)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>We explored the impact of obesity, body composition, and genetic polymorphisms on the pharmacokinetics (PK) of daunorubicin in children with cancer.&lt;h4>Patients and methods&lt;/h4>Patients ≤21 years receiving daunorubicin as an infusion of any duration &lt;24 h for any type of cancer were eligible. Plasma drug concentrations were measured by high-performance liquid chromatography. Body composition was measured by dual-energy X-ray absorptiometry. Obesity was defined as a BMI >95% for age or as body fat >30%. NONMEM was used to perform PK model fitting. The Affymetrix DMET chip was used for genotyping. The impact of genetic polymorphisms was investigated using SNP/haplotype association analysis with estimated individual PK parameters.&lt;h4>Results&lt;/h4>A total of 107 subjects were en</pubmed_abstract><journal>Cancer chemotherapy and pharmacology</journal><pubmed_title>Pharmacokinetics and pharmacogenomics of daunorubicin in children: a report from the Children's Oncology Group.</pubmed_title><pmcid>PMC4282931</pmcid><funding_grant_id>U10 CA098543</funding_grant_id><funding_grant_id>UG1 CA189955</funding_grant_id><funding_grant_id>GM61393</funding_grant_id><funding_grant_id>U10 CA180886</funding_grant_id><funding_grant_id>U01 GM061393</funding_grant_id><funding_grant_id>F32CA165823</funding_grant_id><funding_grant_id>F32 CA165823</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><funding_grant_id>U10 CA095861</funding_grant_id><funding_grant_id>U10 CA098413</funding_grant_id><pubmed_authors>Devidas M</pubmed_authors><pubmed_authors>Sung L</pubmed_authors><pubmed_authors>Dolan ME</pubmed_authors><pubmed_authors>Thompson P</pubmed_authors><pubmed_authors>Lorier R</pubmed_authors><pubmed_authors>Delaney SM</pubmed_authors><pubmed_authors>Wheeler HE</pubmed_authors><pubmed_authors>Broeckel U</pubmed_authors><pubmed_authors>Berg SL</pubmed_authors><pubmed_authors>Reaman GH</pubmed_authors><pubmed_authors>Scorsone K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacokinetics and pharmacogenomics of daunorubicin in children: a report from the Children's Oncology Group.</name><description>&lt;h4>Purpose&lt;/h4>We explored the impact of obesity, body composition, and genetic polymorphisms on the pharmacokinetics (PK) of daunorubicin in children with cancer.&lt;h4>Patients and methods&lt;/h4>Patients ≤21 years receiving daunorubicin as an infusion of any duration &lt;24 h for any type of cancer were eligible. Plasma drug concentrations were measured by high-performance liquid chromatography. Body composition was measured by dual-energy X-ray absorptiometry. Obesity was defined as a BMI >95% for age or as body fat >30%. NONMEM was used to perform PK model fitting. The Affymetrix DMET chip was used for genotyping. The impact of genetic polymorphisms was investigated using SNP/haplotype association analysis with estimated individual PK parameters.&lt;h4>Results&lt;/h4>A total of 107 subjects were en</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2026-04-29T12:13:32.095Z</modification><creation>2019-03-27T01:42:40Z</creation></dates><accession>S-EPMC4282931</accession><cross_references><pubmed>25119182</pubmed><doi>10.1007/s00280-014-2535-4</doi></cross_references></HashMap>