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Tissue-simulating Phantoms for Assessing Potential Near-infrared Fluorescence Imaging Applications in Breast Cancer Surgery
Published on: September 19, 2014
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Characterizing the detection threshold for optical imaging in surgical oncology
Andrew C Prince1, Aditi Jani1, Melissa Korb2
1School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Journal of Surgical Oncology
|June 20, 2017
Summary
Antibody-based fluorescence imaging can detect as few as 4.2 x 10^4 cancer cells, supporting its use for identifying subclinical disease during surgery.
Area of Science:
- Oncology
- Medical Imaging
- Molecular Diagnostics
Background:
- Optical imaging is increasingly used in surgery for cancer resection.
- The sensitivity of fluorescence imaging for detecting minimal residual disease requires characterization.
Purpose of the Study:
- To determine the minimum number of cancer cells detectable by antibody-based fluorescence imaging.
- To assess the sensitivity of cetuximab-IRDye800CW for detecting various cancer cell lines.
Main Methods:
- In vitro incubation of four cancer cell lines (2LMP, COLO-205, MiaPaca-2, SCC-1) with cetuximab-IRDye800CW.
- Subcutaneous implantation of serially diluted cancer cells in mice.
- Imaging of tumors using Pearl Impulse and Xenogen IVIS 100 systems.
- Scatchard analysis to determine receptor density and kinetics.
Main Results:
- Fluorescence imaging detected a minimum of 4.2 x 10^4 to 9.5 x 10^4 2LMP cells, 1.9 x 10^5 to 4.5 x 10^5 MiaPaca-2 cells, and 2.4 x 10^4 to 6.7 x 10^4 SCC-1 cells.
- COLO-205 cells were not identifiable under tested conditions.
- Higher epidermal growth factor receptor (EGFR)-mediated uptake of cetuximab correlated with improved detection sensitivity.
Conclusions:
- Cetuximab-IRDye800CW fluorescence imaging demonstrates potential for sensitive detection of subclinical cancer cells.
- The findings support the clinical utility of this technique for localizing minimal disease in surgical settings.

