Overview

Molecular Fluorescence Endoscopy in Patients With Familial Adenomatous Polyposis, Using Bevacizumab-IRDye800CW

Status:
Completed
Trial end date:
2015-10-01
Target enrollment:
0
Participant gender:
All
Summary
There is a need for better visualization of polyps during surveillance endoscopy in patients with hereditary colon cancer syndromes like Familial Adenomatous Polyposis (FAP) and Lynch Syndrome (LS), to improve the adenoma detection rate. Optical molecular imaging of adenoma associated biomarkers is a promising technique to accommodate this need. The biomarker Vascular Endothelial Growth Factor (VEGF) is overexpressed in adenomatous colon tissue versus normal tissue and has proven to be a valid target for molecular imaging. The University Medical Center Groningen (UMCG) developed a fluorescent tracer by labeling the VEGF-targeting humanized monoclonal antibody bevacizumab, currently used in anti-cancer therapy, with the fluorescent dye IRDye800CW. The investigators hypothesize that when bevacizumab-IRDye800CW is administered to patients, it accumulates in VEGF expressing adenomas, enabling adenoma visualization using a newly developed near-infrared (NIR) fluorescence endoscopy platform (NL43407.042.13). This hypothesis will be tested in this feasibility study, next to the determination of the optimal tracer dose.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Medical Center Groningen
Treatments:
Bevacizumab
Criteria
Inclusion Criteria:

- Patients with genetically or clinically proven Familial Adenomatous Polyposis.
Genetically proven: Adenomatous Polyposis Coli (APC)-mutation identified. Clinically
proven: more than 100 colorectal polyps at diagnosis

- Age 18 to 70 years

- Written informed consent

- Adequate potential for follow-up

Exclusion Criteria:

- Medical or psychiatric conditions that compromise the patient's ability to give
informed consent

- Proctocolectomy

- MutYH mutation

- Concurrent uncontrolled medical conditions

- Pregnant or lactating women. Documentation of a negative pregnancy test must be
available for woman of childbearing potential. Woman of childbearing potential are
pre-menopausal women with intact reproductive organs and women less than two years
after menopause.