Show simple item record

dc.contributor.authorJoerger, M.en
dc.contributor.authorHuitema, A. D. R.en
dc.contributor.authorRichel, D. J.en
dc.contributor.authorDittrich, C.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorBriassoulis, E. Chen
dc.contributor.authorVermorken, J. B.en
dc.contributor.authorStrocchi, E.en
dc.contributor.authorMartoni, A.en
dc.contributor.authorSorio, R.en
dc.contributor.authorSleeboom, H. P.en
dc.contributor.authorIzquierdo, M. A.en
dc.contributor.authorJodrell, D. I.en
dc.contributor.authorCalvert, H.en
dc.contributor.authorBoddy, A. V.en
dc.contributor.authorHollema, H.en
dc.contributor.authorFéty, R.en
dc.contributor.authorVijgh, W. J. F. Van Deren
dc.contributor.authorHempel, G.en
dc.contributor.authorChatelut, E.en
dc.contributor.authorKarlsson, M.en
dc.contributor.authorWilkins, J.en
dc.contributor.authorTranchand, B.en
dc.contributor.authorSchrijvers, A. H. G. J.en
dc.contributor.authorTwelves, C.en
dc.contributor.authorBeijnen, J. H.en
dc.contributor.authorSchellens, J. H. M.en
dc.creatorJoerger, M.en
dc.creatorHuitema, A. D. R.en
dc.creatorRichel, D. J.en
dc.creatorDittrich, C.en
dc.creatorPavlidis, Nicholasen
dc.creatorBriassoulis, E. Chen
dc.creatorVermorken, J. B.en
dc.creatorStrocchi, E.en
dc.creatorMartoni, A.en
dc.creatorSorio, R.en
dc.creatorSleeboom, H. P.en
dc.creatorIzquierdo, M. A.en
dc.creatorJodrell, D. I.en
dc.creatorCalvert, H.en
dc.creatorBoddy, A. V.en
dc.creatorHollema, H.en
dc.creatorFéty, R.en
dc.creatorVijgh, W. J. F. Van Deren
dc.creatorHempel, G.en
dc.creatorChatelut, E.en
dc.creatorKarlsson, M.en
dc.creatorWilkins, J.en
dc.creatorTranchand, B.en
dc.creatorSchrijvers, A. H. G. J.en
dc.creatorTwelves, C.en
dc.creatorBeijnen, J. H.en
dc.creatorSchellens, J. H. M.en
dc.date.accessioned2018-06-22T09:53:42Z
dc.date.available2018-06-22T09:53:42Z
dc.date.issued2007
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41976
dc.description.abstractPurpose: Paclitaxel and carboplatin are frequently used in advanced ovarian cancer following cytoreductive surgery. Threshold models have been used to predict paclitaxel pharmacokinetic-pharmacodynamics, whereas the time above paclitaxel plasma concentration of 0.05 to 0.2 μmol/L (t C > 0.05-0.2) predicts neutropenia. The objective of this study was to build a population pharmacokinetic-pharmacodynamic model of paclitaxel/carboplatin in ovarian cancer patients. Experimental Design: One hundred thirty-nine ovarian cancer patients received paclitaxel (175 mg/m 2) over 3 h followed by carboplatin area under the concentration-time curve 5 mg/mL*min over 30 min. Plasma concentration-time data were measured, and data were processed using nonlinear mixed-effect modeling. Semiphysiologic models with linear or sigmoidal maximum response and threshold models were adapted to the data. Results: One hundred five patients had complete pharmacokinetic and toxicity data. In 34 patients with measurable disease, objective response rate was 76%. Neutrophil and thrombocyte counts were adequately described by an inhibitory linear response model. Paclitaxel t C > 0.05 was significantly higher in patients with a complete (91.8 h) or partial (76.3 h) response compared with patients with progressive disease (31.5 h; P = 0.02 and 0.05, respectively). Patients with paclitaxel tC > 0.05 > 61.4 h (mean value) had a longer time to disease progression compared with patients with paclitaxel tC > 0.05 0.05 was a good predictor for severe neutropenia (P = 0.01), whereas carboplatin exposure (Cmax and area under the concentration-time curve) was the best predictor for thrombocytopenia (P 0.05 is a good predictive marker for severe neutropenia and clinical outcome, whereas carboplatin exposure is a good predictive marker for thrombocytopenia. ©2007 American Association for Cancer Research.en
dc.language.isoengen
dc.sourceClinical Cancer Researchen
dc.subjectEuropeen
dc.subjectArticleen
dc.subjectAntineoplastic agentsen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectCancer combination chemotherapyen
dc.subjectCarboplatinen
dc.subjectDisease progressionen
dc.subjectDrug responseen
dc.subjectOvarian neoplasmsen
dc.subjectOvary canceren
dc.subjectPaclitaxelen
dc.subjectPredictive value of testsen
dc.subjectPriority journalen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectDiarrheaen
dc.subjectNeutropeniaen
dc.subjectOndansetronen
dc.subjectThrombocytopeniaen
dc.subjectDexamethasoneen
dc.subjectTreatment outcomeen
dc.subjectSide effecten
dc.subjectVomitingen
dc.subjectBlood toxicityen
dc.subjectNauseaen
dc.subjectDrug dose reductionen
dc.subjectMultiple cycle treatmenten
dc.subjectAminotransferase blood levelen
dc.subjectGranisetronen
dc.subjectIleusen
dc.subjectPeripheral neuropathyen
dc.subjectArea under curveen
dc.subjectDeep vein thrombosisen
dc.subjectClemastineen
dc.subjectDrug designen
dc.subjectKineticsen
dc.subjectMetoclopramideen
dc.subjectNeutrophil counten
dc.subjectPharmacodynamicsen
dc.subjectThrombocyte counten
dc.titlePopulation pharmacokinetics and pharmacodynamics of paclitaxel and carboplatin in ovarian cancer patients: A study by the European organization for research and treatment of cancer-pharmacology and molecular mechanisms group and new drug development groupen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1158/1078-0432.CCR-07-0064
dc.description.volume13
dc.description.issue21
dc.description.startingpage6410
dc.description.endingpage6418
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.gnosis.orcid0000-0002-2195-9961


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record