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Clinical Trial Summary

We will observe if ICG fluorescence correlates with margins of breast tumours after iv injection of the contrast agent


Clinical Trial Description

In the operating room: ICG 0.25 mg/kg will be given as an iv injection at least 20 minutes before the beginning of the operation. The surgeon will remove the tumour (and the axillary lymph nodes) as usual. Optionally, peroperative "in vivo" imaging of the dissection of the tumour using the PDE camera will be performed. In the Laboratory of Pathology: The "fresh" tumorectomy piece will be processed as usual, and the thick sections for the evaluation of the margins as well as the tissues samples from each margins will be imaged using the PDE in comparison with the fluorescence in the mid part of the tumour and the fluorescent areas will be so delimited (and later analyzed in comparison with standards of known fluorescence intensity). After fixation, the tumoral tissues will be thereafter processed "as usual". If fluorescent foci are identified at the level of the axillary piece (in case of CALND), they will be dissected and processed as other lymph nodes. Additionally, metastatic lymph nodes -if present- will also be controlled for their microscopic fluorescence or not. Using the near-infrared fluorescence microscope, the slides corresponding to the macroscopically fluorescent structures will be analyzed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02027818
Study type Interventional
Source Jules Bordet Institute
Contact
Status Completed
Phase Phase 2
Start date January 2014
Completion date October 2014

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