Home Duke University Press
 QUICK SEARCH:   [advanced]


     
  Home | Help | Feedback | Subscriptions | Archive | Search | Advance Publication


First published on October 29, 2008
A more recent version of this article appeared on January 1, 2009
Neuro Oncol 2008, DOI:10.1215/15228517-2008-088
This Article
Right arrow Advance Publication Full Text (PDF)
Right arrow All Versions of this Article:
11/3/301    most recent
15228517-2008-088v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhou, O.
Right arrow Articles by Gallo, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
© Copyright 2008 by the Society for Neuro-Oncology

Received May 20, 2008
Accepted July 22, 2008

Basic and Translational Investigations

Differential effect of sunitinib on the distribution of temozolomide in an orthotopic glioma model

Oingyu Zhou 1 James M. Gallo 1*

1 Department of Pharmaceutical Sciences, School of Pharmacy, Temple University, Philadelphia, PA

* To whom correspondence should be addressed. E-mail: jmgallo{at}temple.edu.


   Abstract

Normalization of tumor vasculature by antiangiogenic agents may improve the delivery of cytotoxic drugs to the tumor, leading to more effective therapy. In this study, pharmacokinetic and pharmacodynamic approaches were utilized to investigate how sunitinib at different dose levels affects brain distribution of temozolomide (TMZ), and to ascertain the relationship between intratumoral TMZ concentrations and tumor vascularity in an orthotropic human glioma model. Three groups of intracerebral U87MG tumor-bearing mice were given either vehicle, 20 mg/kg/d or 60 mg/kg/d sunitinib, for 7 days before receiving a steady-state regimen of TMZ that consisted of an IV bolus and a 3-h intraarterial infusion. TMZ concentrations in plasma, normal brain and brain tumor were determined, and several biomarkers related to the antiangiogenic activity of sunitinib were examined. TMZ distribution in the normal brain as indicated by the brain-to-plasma steady-state TMZ concentration ratios was analogous between the three treatment groups. The brain tumor-to-plasma steady-state TMZ concentration (ss Ct/Cp) ratio was significantly increased in the 20 mg/kg sunitinib group (0.98 ± 0.17) as compared with the control (0.76 ± 0.17) and 60 mg/kg sunitinib (0.68 ± 0.09) groups. The ss Ct/Cp ratios were significantly correlated with the Vascular Normalization Index (VNI), derived from the expression of CD31, collagen IV, and {alpha}-smooth muscle actin, which represents the fraction of functioning vessels out of the total tumor vessels. In conclusion, the effect of sunitinib on the brain tumor distribution of TMZ was dose-dependent, and indicated optimal tumor exposure was achieved at a lower dose and associated with the VNI.

Key Words: antiangiogenic therapy, combination chemotherapy, pharmacokinetics, temozolomide, sunitinib, vascular normalization


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?





  Home | Help | Feedback | Subscriptions | Archive | Search | Advance Publication


Copyright 2008 by Society for Neuro-Oncology