Intravascular contrast agent-enhanced MRI measuring contrast clearance and tumor blood volume and the effects of vascular modifiers in an experimental tumor

Int J Radiat Oncol Biol Phys. 2005 Mar 15;61(4):1208-15. doi: 10.1016/j.ijrobp.2004.12.020.

Abstract

Purpose: To examine the feasibility of using the MRI blood pool agent NC100150 for evaluation of tumor blood volume (TBV) estimates by both dynamic contrast-enhanced MRI (DCE-MRI) and susceptibility contrast MRI assays in an experimental tumor. Contrast agent clearance (K(trans); depends on perfusion and permeability) from the DCE-MRI time curves was estimated, and changes in TBV and K(trans) were measured after administration of two drugs that reduce perfusion by different mechanisms.

Methods and materials: The DCE-MRI experiments were simulated with expected physiologic values for the C3H mouse mammary carcinoma. The C3H tumor was examined by DCE-MRI and susceptibility contrast MRI with NC100150 (NC100150 Injection, Clariscan; Amersham Health, Oslo, Norway) after treatment with either hydralazine or combretastatin (Oxigene, Boston, MA).

Results: Simulations showed that reliable estimates of changes in TBV and K(trans) could be performed with DCE-MRI. Hydralazine was shown to reduce TBV as measured by both assays and to reduce K(trans). Dynamic contrast-enhanced MRI also suggested that TBV and K(trans) were reduced in combretastatin-treated tumors, and the TBV reduction was confirmed by susceptibility contrast MRI. Data suggested the drug to affect mainly the total TBV, whereas microvessels as such seemed less altered.

Conclusion: The study supports the use of the combined DCE-MRI and susceptibility contrast MRI assay with a blood pool agent in characterizing tumors and their response to treatment.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / therapeutic use
  • Bibenzyls / therapeutic use
  • Contrast Media* / pharmacokinetics
  • Dextrans
  • Female
  • Ferrosoferric Oxide
  • Hydralazine / therapeutic use
  • Iron* / pharmacokinetics
  • Magnetic Resonance Imaging / methods*
  • Magnetite Nanoparticles
  • Mammary Neoplasms, Experimental / blood supply*
  • Mammary Neoplasms, Experimental / drug therapy
  • Mice
  • Mice, Inbred C3H
  • Oxides* / pharmacokinetics
  • Stilbenes / therapeutic use
  • Vasodilator Agents / therapeutic use

Substances

  • Antineoplastic Agents, Phytogenic
  • Bibenzyls
  • Contrast Media
  • Dextrans
  • Magnetite Nanoparticles
  • Oxides
  • Stilbenes
  • Vasodilator Agents
  • ferumoxtran-10
  • Hydralazine
  • combretastatin
  • Iron
  • Ferrosoferric Oxide