Research Papers:
Fluorescence-guided surgery for cancer patients: a proof of concept study on human xenografts in mice and spontaneous tumors in pets
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Abstract
Eliane Mery1,*, Muriel Golzio2,*, Stephanie Guillermet3, Didier Lanore4, Augustin Le Naour1, Benoît Thibault1, Anne Françoise Tilkin-Mariamé1, Elizabeth Bellard2, Jean Pierre Delord1, Denis Querleu1, Gwenael Ferron1,* and Bettina Couderc1,*
1Institut Claudius Regaud –IUCT Oncopole, University Toulouse III, Toulouse, France
2Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, Toulouse, France
3Fluoptics SAS, Grenoble, France
4Clinique vétérinaire Alliance, Bordeaux, France
*These authors have contributed equally to this work
Correspondence to:
Bettina Couderc, email: [email protected]
Keywords: tumor targeting; optical imaging; fluorescence-guided surgery; integrins; spontaneous animal models
Received: July 27, 2017 Accepted: October 28, 2017 Published: November 30, 2017
ABSTRACT
Surgery is often the first treatment option for patients with cancer. Patient survival essentially depends on the completeness of tumor resection. This is a major challenge, particularly in cases of peritoneal carcinomatosis, where tumors are widely disseminated in the large peritoneal cavity. Any development to help surgeons visualize these residual cells would improve the completeness of the surgery. For non-disseminated tumors, imaging could be used to ensure that the tumor margins and the draining lymph nodes are free of tumor deposits.
Near-infrared fluorescence imaging has been shown to be one of the most convenient imaging modalities. Our aim was to evaluate the efficacy of a near-infrared fluorescent probe targeting the αvβ3 integrins (Angiostamp™) for intraoperative detection of tumors using the Fluobeam® device.
We determined whether different human tumor nodules from various origins could be detected in xenograft mouse models using both cancer cell lines and patient-derived tumor cells. We found that xenografts could be imaged by fluorescent staining irrespective of their integrin expression levels. This suggests imaging of the associated angiogenesis of the tumor and a broader potential utilization of Angiostamp™. We therefore performed a veterinary clinical trial in cats and dogs with local tumors or with spontaneous disseminated peritoneal carcinomatosis. Our results demonstrate that the probe can specifically visualize both breast and ovarian nodules, and suggest that Angiostamp™ is a powerful fluorescent contrast agent that could be used in both human and veterinary clinical trials for intraoperative detection of tumors.
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