4.5 Article

Quantitative Assessment of Tumor Blood Flow Changes in a Murine Breast Cancer Model After Adriamycin Chemotherapy Using Contrast-Enhanced Destruction-Replenishment Sonography

Journal

JOURNAL OF ULTRASOUND IN MEDICINE
Volume 32, Issue 4, Pages 683-690

Publisher

WILEY
DOI: 10.7863/jum.2013.32.4.683

Keywords

chemotherapy; contrast-enhanced sonography; destruction-reperfusion; tumor

Funding

  1. National Natural Science Foundation of China [30900369, 81071168]
  2. Fundamental Research Funds for the Central Universities [09ykpy56]

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Objectives-The purpose of the study was to detect tumor blood flow changes after chemotherapy with contrast-enhanced destruction-replenishment sonography. Methods-Twenty-four MCF-7 breast cancer-bearing nude mice were included in this study. Animals received either adriamycin or sterile saline and underwent contrast-enhanced sonography before and after treatment using a destruction-replenishment technique. A monoexponential function, y = A(1 - e(-beta t)), was used to fit the replenishment kinetics, where the plateau signal intensity A reflects the percent blood volume; the time constant 13 reflects the average speed of blood; and their product A*beta reflects the nutrient blood flow. Tumor blood perfusion was compared to measurements of cell density and microvascular density: Results-Volumes of the treated tumors were significantly reduced after 7 days of adriamycin treatment compared with the control tumors (P < .001). Before adriamycin administration, there was no significant difference in blood perfusion between the treated and control groups (P > .05). Treatment with adriamycin resulted in a significant decrease in A, beta, andA*beta (P < .001) compared with the control tumors. The tumor cell density and microvascular density estimated by pathologic slices were significantly lower in the treated tumors than in the control tumors (P < .001). Conclusions-Quantification of tumor blood flow using contrast-enhanced destruction-replenishment sonography shows the potential to evaluate tumor responses to chemotherapy.

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