Cargando…

Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial

Altered pharmacokinetics of antibody drugs has been reported in advanced gastric cancer (AGC). We aim to evaluate bevacizumab pharmacokinetics in AGC from the Phase III trial (AVAGAST), and explore the influence of patient variables. Bevacizumab concentrations (Cp) were measured in plasma samples ta...

Descripción completa

Detalles Bibliográficos
Autores principales: Han, Kelong, Jin, Jin, Maia, Mauricio, Lowe, John, Sersch, Martina A., Allison, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147052/
https://www.ncbi.nlm.nih.gov/pubmed/24942210
http://dx.doi.org/10.1208/s12248-014-9631-6
_version_ 1782332382210162688
author Han, Kelong
Jin, Jin
Maia, Mauricio
Lowe, John
Sersch, Martina A.
Allison, David E.
author_facet Han, Kelong
Jin, Jin
Maia, Mauricio
Lowe, John
Sersch, Martina A.
Allison, David E.
author_sort Han, Kelong
collection PubMed
description Altered pharmacokinetics of antibody drugs has been reported in advanced gastric cancer (AGC). We aim to evaluate bevacizumab pharmacokinetics in AGC from the Phase III trial (AVAGAST), and explore the influence of patient variables. Bevacizumab concentrations (Cp) were measured in plasma samples taken following disease progression from 162 patients (7.5 mg/kg every 3 weeks). Predicted Cp [median and 90% prediction interval] was simulated using the population pharmacokinetic model established for other cancers (PPK model) and compared to observed Cp. Bevacizumab clearance was estimated using NONMEM and compared between subgroups. Patient characteristics of AGC are similar to other cancers except for lower body weight despite higher percentage of males. Eighty-five percent of observed Cp was below the median predicted Cp and 38% below the lower boundary of the 90% prediction interval. Median bevacizumab clearance in AGC was 4.5 versus 3 mL/day/kg in other cancers. Bevacizumab clearance was significantly faster (p < 0.05) in patients without gastrectomy (n = 42) or lower albumin. Clearance appeared to be faster in patients with lower total protein, higher ECOG scores, more metastatic sites, and poorer response. No significant difference in bevacizumab concentrations and clearance was observed between Asian and Non-Asian patients. AGC patients exhibited significantly lower bevacizumab exposure due to an approximate 50% increase in clearance versus other cancers. Bevacizumab is cleared faster in patients without prior gastrectomy. No significant difference in bevacizumab pharmacokinetics was observed between Asian and Non-Asian patients. The underlying mechanism for faster bevacizumab clearance in AGC is unknown and warrants further research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1208/s12248-014-9631-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4147052
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-41470522014-08-28 Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial Han, Kelong Jin, Jin Maia, Mauricio Lowe, John Sersch, Martina A. Allison, David E. AAPS J Research Article Altered pharmacokinetics of antibody drugs has been reported in advanced gastric cancer (AGC). We aim to evaluate bevacizumab pharmacokinetics in AGC from the Phase III trial (AVAGAST), and explore the influence of patient variables. Bevacizumab concentrations (Cp) were measured in plasma samples taken following disease progression from 162 patients (7.5 mg/kg every 3 weeks). Predicted Cp [median and 90% prediction interval] was simulated using the population pharmacokinetic model established for other cancers (PPK model) and compared to observed Cp. Bevacizumab clearance was estimated using NONMEM and compared between subgroups. Patient characteristics of AGC are similar to other cancers except for lower body weight despite higher percentage of males. Eighty-five percent of observed Cp was below the median predicted Cp and 38% below the lower boundary of the 90% prediction interval. Median bevacizumab clearance in AGC was 4.5 versus 3 mL/day/kg in other cancers. Bevacizumab clearance was significantly faster (p < 0.05) in patients without gastrectomy (n = 42) or lower albumin. Clearance appeared to be faster in patients with lower total protein, higher ECOG scores, more metastatic sites, and poorer response. No significant difference in bevacizumab concentrations and clearance was observed between Asian and Non-Asian patients. AGC patients exhibited significantly lower bevacizumab exposure due to an approximate 50% increase in clearance versus other cancers. Bevacizumab is cleared faster in patients without prior gastrectomy. No significant difference in bevacizumab pharmacokinetics was observed between Asian and Non-Asian patients. The underlying mechanism for faster bevacizumab clearance in AGC is unknown and warrants further research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1208/s12248-014-9631-6) contains supplementary material, which is available to authorized users. Springer US 2014-06-19 /pmc/articles/PMC4147052/ /pubmed/24942210 http://dx.doi.org/10.1208/s12248-014-9631-6 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Article
Han, Kelong
Jin, Jin
Maia, Mauricio
Lowe, John
Sersch, Martina A.
Allison, David E.
Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title_full Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title_fullStr Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title_full_unstemmed Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title_short Lower Exposure and Faster Clearance of Bevacizumab in Gastric Cancer and the Impact of Patient Variables: Analysis of Individual Data from AVAGAST Phase III Trial
title_sort lower exposure and faster clearance of bevacizumab in gastric cancer and the impact of patient variables: analysis of individual data from avagast phase iii trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147052/
https://www.ncbi.nlm.nih.gov/pubmed/24942210
http://dx.doi.org/10.1208/s12248-014-9631-6
work_keys_str_mv AT hankelong lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial
AT jinjin lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial
AT maiamauricio lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial
AT lowejohn lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial
AT serschmartinaa lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial
AT allisondavide lowerexposureandfasterclearanceofbevacizumabingastriccancerandtheimpactofpatientvariablesanalysisofindividualdatafromavagastphaseiiitrial