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  <controlfield tag="005">20180317142635.0</controlfield>
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  <controlfield tag="008">170323e20111201xx      s     000 0 eng  </controlfield>
  <datafield tag="024" ind1="7" ind2="0">
   <subfield code="a">10.1007/s11095-011-0499-1</subfield>
   <subfield code="2">doi</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s11095-011-0499-1</subfield>
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  <datafield tag="245" ind1="0" ind2="0">
   <subfield code="a">Functional and Clinical Evidence of the Influence of Sorafenib Binding to Albumin on Sorafenib Disposition in Adult Cancer Patients</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Michel Tod, Olivier Mir, Natacha Bancelin, Romain Coriat, Audrey Thomas-Schoemann, Fabrice Taieb, Pascaline Boudou-Rouquette, Stanislas Ropert, Judith Michels, Halim Abbas, Jean Durand, Alain Dauphin, Michel Vidal, Francois Goldwasser, Benoit Blanchet]</subfield>
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   <subfield code="a">Purpose: Sorafenib, an oral multitargeted tyrosine kinase inhibitor, is highly bound to plasma proteins (&gt;99.5%). Little is known about the influence of variations in sorafenib protein binding on its disposition. The aims of this study were to characterize in vitro sorafenib binding properties to albumin using the quenching fluorescence method and investigate the influence of albuminemia and bilirubinemia on sorafenib disposition in 54 adult cancer patients. Results: In vitro estimate of sorafenib dissociation constant (Kd) for albumin was 0.22μM [CI95 0.20-0.23]. In physiological conditions, sorafenib unbound fraction would increase 1.7-fold as albuminemia decreased from 45g/L (680μM) to 30g/L (453μM). In presence of bilirubin, apparent Kd of sorafenib was ~1.5-fold greater for bilirubin/albumin molar ratio of 1:4. In clinical settings, median sorafenib clearance (CL) was 1.42L/h (0.75-2.13L/h). In univariate analysis, sex, body mass index, and albuminemia were associated with CL (p = 0.04, 0.048, and 0.008, respectively). In multivariate analysis, albuminemia (p = 0.0036) was the single parameter independently associated with CL. Conclusion: These findings highlight the major influence of albuminemia on sorafenib clearance and its disposition in cancer patients.</subfield>
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  <datafield tag="540" ind1=" " ind2=" ">
   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">albumin</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">cancer</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">drug disposition</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">protein binding</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">sorafenib</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">AAG : α1-acid glycoprotein</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">ALP : alkaline phosphatase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">ALT : aspartate alaninetransferase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">AST : aspartate aminotransferase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Bmax : common binding capacity</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BMI : body mass index</subfield>
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  </datafield>
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   <subfield code="a">Cb : bound drug concentration</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">CL : total clearance</subfield>
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   <subfield code="a">CRP : protein C-reactive</subfield>
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   <subfield code="a">Ct : total concentration of drug</subfield>
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   <subfield code="a">CU : unbound concentration of drug</subfield>
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   <subfield code="a">CV : coefficient of variation</subfield>
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   <subfield code="a">DMSO : dimethyl sulfoxide</subfield>
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   <subfield code="a">fu : unbound fraction</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">GGT : Gamma-glutamyl transpeptidase</subfield>
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   <subfield code="a">HSA : human serum albumin</subfield>
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   <subfield code="a">ICD : induced circular dichroism</subfield>
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   <subfield code="a">Kd : dissociation constant</subfield>
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   <subfield code="a">Kdapp : apparent dissociation constant </subfield>
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   <subfield code="a">Ki : inhibitor constant</subfield>
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   <subfield code="a">Lt : concentration of interacting ligand</subfield>
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   <subfield code="a">MYR : myristic acid</subfield>
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   <subfield code="a">PDGFR : platelet-derived growth factor receptor</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Pu : unbound protein concentration</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">VEGFR : vascular endothelial growth factor receptor</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">λ exc : maximum excitation wavelength</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">λ max : maximum emission wavelength</subfield>
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   <subfield code="a">Tod</subfield>
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   <subfield code="a">Mir</subfield>
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   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
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   <subfield code="a">Bancelin</subfield>
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   <subfield code="u">Laboratoire de Pharmacologie-Toxicologie, Service de Pharmacie, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Coriat</subfield>
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   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
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   <subfield code="a">Thomas-Schoemann</subfield>
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   <subfield code="u">Université Paris Descartes, 75005, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Taieb</subfield>
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   <subfield code="u">Laboratoire de Pharmacologie-Toxicologie, Service de Pharmacie, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Boudou-Rouquette</subfield>
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   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Ropert</subfield>
   <subfield code="D">Stanislas</subfield>
   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Michels</subfield>
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   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
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   <subfield code="a">Abbas</subfield>
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   <subfield code="u">Laboratoire de Pharmacologie-Toxicologie, Service de Pharmacie, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Durand</subfield>
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   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
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  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Dauphin</subfield>
   <subfield code="D">Alain</subfield>
   <subfield code="u">Laboratoire de Pharmacologie-Toxicologie, Service de Pharmacie, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Vidal</subfield>
   <subfield code="D">Michel</subfield>
   <subfield code="u">Université Paris Descartes, 75005, Paris, France</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Goldwasser</subfield>
   <subfield code="D">Francois</subfield>
   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Blanchet</subfield>
   <subfield code="D">Benoit</subfield>
   <subfield code="u">Centre d'Études et de Recours sur les Inhibiteurs de l'Angiogénèse, AP-HP, Hôpital Cochin, 75014, Paris, France</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Pharmaceutical Research</subfield>
   <subfield code="d">Springer US; http://www.springer-ny.com</subfield>
   <subfield code="g">28/12(2011-12-01), 3199-3207</subfield>
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