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Pharmacokinetics of etoposide in cancer patients treated with high-dose etoposide and with dexrazoxane (ICRF-187) as a rescue agent
Authors:Patricia?E.?Schroeder,Kenneth?Francis?Hofland,Peter?Buhl?Jensen,Maxwell?Sehested,Seppo?W.?Langer,Brian?B.?Hasinoff  author-information"  >  author-information__contact u-icon-before"  >  mailto:B_Hasinoff@UManitoba.ca"   title="  B_Hasinoff@UManitoba.ca"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Faculty of Pharmacy, University of Manitoba, 50 Sifton Road, Winnipeg, Manitoba, R3T 2N2, Canada;(2) Laboratory of Experimental Medical Oncology, The Laboratory Center, The National University Hospital, 2100 Copenhagen, Denmark;(3) The Finsen Center and Department of Pathology, The National University Hospital, 2100 Copenhagen, Denmark
Abstract:Purpose The pharmacokinetics of etoposide were studied in cancer patients with brain metastases treated with high-dose etoposide in order to determine if the pharmacokinetics were altered by the use of dexrazoxane as a rescue agent to reduce the extracerebral toxicity of etoposide.Methods Etoposide plasma levels were determined by HPLC.Results The etoposide pharmacokinetics described by a monophasic first-order elimination model were found to be similar to other reported data in other settings and at similar doses.Conclusions The pharmacokinetics of etoposide were unaffected by dexrazoxane rescue.Abbreviations AUC0–infin Area under the curve from time zero to infinity - Cmax Maximum plasma concentration of drug - Cltot Total plasma clearance - HPLC High-pressure liquid chromatography - Poct Octanol-water partition coefficient - t1/2beta Beta phase plasma elimination half-time - tr Retention time Patricia Schroeder and Kenneth Hofland contributed equally to this work.
Keywords:Etoposide  Dexrazoxane  Pharmacokinetics  Toxicity  Rescue
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