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.

Abstract

Insights

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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