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Sökning: id:"swepub:oai:DiVA.org:uu-410140" > Prediction of expos...

Prediction of exposure-driven myelotoxicity of continuous infusion 5-fluorouracil by a semi-physiological pharmacokinetic-pharmacodynamic model in gastrointestinal cancer patients

Arshad, Usman (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Ploylearmsaeng, Su-arpa (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Karlsson, Mats (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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Doroshyenko, Oxana (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Langer, Dorothee (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Schömig, Edgar (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Kunze, Sabine (författare)
Univ Hosp Cologne, Dept Radiotherapy, Cologne, Germany
Güner, Semih A. (författare)
Univ Hosp Cologne, Dept Radiotherapy, Cologne, Germany
Skripnichenko, Roman (författare)
Univ Hosp Cologne, Dept Radiotherapy, Cologne, Germany
Ullah, Sami (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Bonn, Inst Pharm, Clin Pharm, Bonn, Germany
Jaehde, Ulrich (författare)
Univ Bonn, Inst Pharm, Clin Pharm, Bonn, Germany
Fuhr, Uwe (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
Jetter, Alexander (författare)
Univ Zurich Hosp, Univ Zurich, Dept Clin Pharmacol & Toxicol, Zurich, Switzerland
Taubert, Max (författare)
Univ Cologne, Fac Med, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany;Univ Cologne, Univ Hosp Cologne, Ctr Pharmacol, Dept Pharmacol 1, Cologne, Germany
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 (creator_code:org_t)
2020-03-09
2020
Engelska.
Ingår i: Cancer Chemotherapy and Pharmacology. - : Springer Science and Business Media LLC. - 0344-5704 .- 1432-0843. ; 85:4, s. 711-722
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • PurposeTo describe 5-fluorouracil (5FU) pharmacokinetics, myelotoxicity and respective covariates using a simultaneous nonlinear mixed effect modelling approach.MethodsThirty patients with gastrointestinal cancer received 5FU 650 or 1000 mg/m2/day as 5-day continuous venous infusion (14 of whom also received cisplatin 20 mg/m2/day). 5FU and 5-fluoro-5,6-dihydrouracil (5FUH2) plasma concentrations were described by a pharmacokinetic model using NONMEM. Absolute leukocyte counts were described by a semi-mechanistic myelosuppression model. Covariate relationships were evaluated to explain the possible sources of variability in 5FU pharmacokinetics and pharmacodynamics.ResultsTotal clearance of 5FU correlated with body surface area (BSA). Population estimate for total clearance was 249 L/h. Clearances of 5FU and 5FUH2 fractionally changed by 77%/m2 difference from the median BSA. 5FU central and peripheral volumes of distribution were 5.56 L and 28.5 L, respectively. Estimated 5FUH2 clearance and volume of distribution were 121 L/h and 96.7 L, respectively. Baseline leukocyte count of 6.86 × 109/L, as well as mean leukocyte transit time of 281 h accounting for time delay between proliferating and circulating cells, was estimated. The relationship between 5FU plasma concentrations and absolute leukocyte count was found to be linear. A higher degree of myelosuppression was attributed to combination therapy (slope = 2.82 L/mg) with cisplatin as compared to 5FU monotherapy (slope = 1.17 L/mg).ConclusionsBSA should be taken into account for predicting 5FU exposure. Myelosuppression was influenced by 5FU exposure and concomitant administration of cisplatin.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

5-Fluorouracil
Pharmacokinetics
Pharmacodynamics
Pharmacogenetics
Myelosuppression

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