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Updated: May 11, 2026

Radionuclide-fluorescence Reporter Gene Imaging to Track Tumor Progression in Rodent Tumor Models
Published on: March 13, 2018
Tumor margin detection using quantitative NIRF molecular imaging targeting EpCAM validated by far red gene reporter
Banghe Zhu1, Grace Wu, Holly Robinson
1Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center, 1825 Pressler Street, Houston, TX, 77030, USA.
Near-infrared fluorescence (NIRF) imaging accurately detects prostate cancer margins using an EpCAM-targeting antibody. This image-guided approach enhances surgical precision, potentially reducing residual disease and improving patient outcomes.
Area of Science:
- Oncology
- Medical Imaging
- Surgical Technology
Background:
- Wide-field surgical excision is standard for cancer removal but risks disfigurement and morbidity near critical structures.
- Accurate tumor margin detection is crucial to minimize residual disease and optimize surgical outcomes.
Purpose of the Study:
- To evaluate the efficacy of near-infrared fluorescence (NIRF) imaging for precise tumor margin detection in prostate cancer.
- To determine if NIRF imaging can guide surgical resection, improving accuracy and reducing complications.
Main Methods:
- An orthotopic human prostate cancer model was utilized.
- NIRF-labeled antibody targeting epithelial cell adhesion molecule (EpCAM) assessed tumor margins.
- Far-red fluorescent gene reporter (iRFP) enabled colocalization for margin assessment.
Main Results:
- Far-red fluorescence demonstrated >96% accuracy compared to standard pathology for primary and metastatic lesions.
- Quantitative NIRF imaging with an EpCAM-targeting antibody significantly improved primary tumor margin detection accuracy versus an isotype control.
Conclusions:
- NIRF molecular imaging offers a promising tool for real-time, accurate assessment of tumor margins.
- This technology has the potential to enhance image-guided surgical resection in oncology.
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