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

Journal Article · · International Journal of Radiation Oncology, Biology and Physics
 [1];  [2];  [1];  [1];  [3];  [4];  [1];  [2]
  1. Experimental Clinical Oncology, Arhus University Hospital, Arhus (Denmark)
  2. Neuroradiology Research Unit, Arhus University Hospital, Arhus (Denmark)
  3. Department of Radiology, Rikshospitalet, Oslo (Norway)
  4. Amersham Health, Oslo (Norway)

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{sup trans}; depends on perfusion and permeability) from the DCE-MRI time curves was estimated, and changes in TBV and K{sup 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{sup trans} could be performed with DCE-MRI. Hydralazine was shown to reduce TBV as measured by both assays and to reduce K{sup trans}. Dynamic contrast-enhanced MRI also suggested that TBV and K{sup 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.

OSTI ID:
20696152
Journal Information:
International Journal of Radiation Oncology, Biology and Physics, Vol. 61, Issue 4; Other Information: DOI: 10.1016/j.ijrobp.2004.12.020; PII: S0360-3016(04)03140-2; Copyright (c) 2005 Elsevier Science B.V., Amsterdam, Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0360-3016
Country of Publication:
United States
Language:
English

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