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The Optimal Imaging Window for Dysplastic Colorectal Polyp Detection Using c-Met-Targeted Fluorescence Molecular
Steven J de Jongh1, Josephina P M Vrouwe2, Floris J Voskuil3
1Department of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, The Netherlands.
Summary
Fluorescence molecular endoscopy (FME) with EMI-137 is safe for detecting colorectal cancer. This technique shows higher fluorescence in lesions, potentially improving polyp detection rates.
Area of Science:
- Medical imaging
- Gastroenterology
- Molecular diagnostics
Background:
- Colorectal polyp detection miss-rate is 22%.
- Fluorescence molecular endoscopy (FME) is an emerging technique to improve detection.
- EMI-137 is a c-Met-targeted fluorescent peptide for FME.
Purpose of the Study:
- Determine the optimal dose-to-imaging interval for FME using EMI-137.
- Assess the safety and feasibility of FME with EMI-137.
- Evaluate EMI-137's efficacy in high-risk colorectal cancer patients.
Main Methods:
- In vivo FME and fluorescence quantification using spectroscopy in 15 patients.
- EMI-137 (0.13 mg/kg) administered intravenously at 1-, 2-, or 3-h intervals.
- Correlation of fluorescence with histopathology, c-Met expression, and in vitro binding specificity.
Main Results:
- FME with EMI-137 was safe and well-tolerated.
- Significantly higher fluorescence in colorectal lesions vs. surrounding tissue across all intervals (TBR 1.53-1.74).
- Fluorescence correlated with histopathology and c-Met overexpression; dose-dependent specific binding confirmed in vitro.
Conclusions:
- FME using EMI-137 is safe and feasible within a 1- to 3-h dose-to-imaging interval.
- No significant clinical differences observed among intervals, but 1-h preferred.
- Future studies to investigate EMI-137 for improved colorectal polyp detection in screening colonoscopies.

