Acute tumor response to ZD6126 assessed by intrinsic susceptibility magnetic resonance imaging

Neoplasia. 2005 May;7(5):466-74. doi: 10.1593/neo.04622.

Abstract

The effective magnetic resonance imaging (MRI) transverse relaxation rate R(2)* was investigated as an early acute marker of the response of rat GH3 prolactinomas to the vascular-targeting agent, ZD6126. Multigradient echo (MGRE) MRI was used to quantify R(2)*, which is sensitive to tissue deoxyhemoglobin levels. Tumor R(2)* was measured prior to, and either immediately for up to 35 minutes, or 24 hours following administration of 50 mg/kg ZD6126. Following MRI, tumor perfusion was assessed by Hoechst 33342 uptake. Tumor R(2)* significantly increased to 116 +/- 4% of baseline 35 minutes after challenge, consistent with an ischemic insult induced by vascular collapse. A strong positive correlation between baseline R(2)* and the subsequent increase in R(2)* measured 35 minutes after treatment was obtained, suggesting that the baseline R(2)* is prognostic for the subsequent tumor response to ZD6126. In contrast, a significant decrease in tumor R(2)* was found 24 hours after administration of ZD6126. Both the 35-minute and 24-hour R(2)* responses to ZD6126 were associated with a decrease in Hoechst 33342 uptake. Interpretation of the R(2)* response is complex, yet changes in tumor R(2)* may provide a convenient and early MRI biomarker for detecting the antitumor activity of vascular-targeting agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Benzimidazoles / pharmacology
  • Female
  • Hemoglobins / chemistry
  • Image Processing, Computer-Assisted
  • Magnetic Resonance Imaging / methods*
  • Microscopy, Fluorescence
  • Neoplasms / diagnosis*
  • Neoplasms / drug therapy*
  • Organophosphorus Compounds / pharmacology*
  • Perfusion
  • Prognosis
  • Prolactinoma / drug therapy
  • Rats
  • Rats, Wistar
  • Time Factors

Substances

  • Antineoplastic Agents
  • Benzimidazoles
  • Hemoglobins
  • N-acetylcochinol-O-phosphate
  • Organophosphorus Compounds
  • deoxyhemoglobin
  • bisbenzimide ethoxide trihydrochloride