| Literature DB >> 27630318 |
Veronika Rachar1, Martin Czejka2, Marie Kitzmueller2, Philipp Buchner2, Maria Lichtneckert3, Richard Greil4, Herbert Geiler5, Christian Dittrich3.
Abstract
AIM: This study focuses on the plasma disposition and metabolic activation of capecitabine (CCB) when administered alone or when combined with cetuximab (CTX). PATIENTS AND METHODS: Twenty-four chemo-naïve patients with KRAS wild-type colorectal cancer were randomized into two arms and received either CCB alone (1,000 mg/m(2) bid p.o.), followed by CCB plus CTX (loading dose (LD)=400 mg/m(2) followed by 250 mg/m(2) weekly i.v. maintenance dose) (Arm A; n=12 patients (patients)) or CCB plus CTX followed by CCB alone (Arm B; n=12 patients). Plasma samples were collected from the cubital vein and CCB, 5'-desoxy-5-fluorocytidine (5'-DFCR) and 5'-desoxy-5 fluorouridine (5'-DFUR) were quantified by a sensitive, selective reversed phase high-performance liquid chromatography (HPLC) assay. Non-compartment pharmacokinetic parameters have been calculated by Phoenix WinNonlin.Entities:
Keywords: Pharmacokinetic study; capecitabine; cetuximab; colorectal cancer; drug-drug interactions
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Year: 2016 PMID: 27630318 DOI: 10.21873/anticanres.11026
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480