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Antiangiogenic antibody improves melanoma detection by fluorescently labeled therapeutic antibodies
Author(s) -
Sweeny Larissa,
Prince Andrew,
Patel Neel,
Moore Lindsay S.,
Rosenthal Eben L.,
Hughley Brian B.,
Warram Jason M.
Publication year - 2016
Publication title -
the laryngoscope
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.181
H-Index - 148
eISSN - 1531-4995
pISSN - 0023-852X
DOI - 10.1002/lary.26215
Subject(s) - antibody , melanoma , medicine , chemistry , cancer research , immunology
Objective Evaluate if vascular normalization with an antiangiogenic monoclonal antibody improves detection of melanoma using fluorescently labeled antibody‐based imaging. Study Design Preclinical. Methods Panitumumab and control IgG were covalently linked to a near‐infrared fluorescent probe (IRDye800CW). Immunodeficient mice with ear xenografts of melanoma cell lines (A375 and SKMEL5) were systemically injected (200 μg, tail vein) with either IgG‐IRDye800CW, panitumumab‐IRDye800CW, or a combination (bevacizumab [5mg/kg], administered 72 hours prepanitumumab‐IRDye800CW) (n = 5). Primary tumors were imaged with open‐field (LUNA, Novadaq, Toronto, Ontario, Canada) and closed‐field (Pearl, LI‐COR Biosciences, Lincoln, NB) imaging devices. Postresection, the concentration of labeled antibody within the tumor (μg/g) was calculated using normalized standards. Results The mean fluorescence within the melanoma tumors was greater for the combination group compared to panitumumab alone for both cell lines ( P < 0.001). The tumor‐to‐background ratio (TBR) for the A375 tumors was greater for the combination (3.4–7.1) compared to the panitumumab alone (3.2–5.0) ( P = 0.04). The TBR for SKMEL5 tumors was greater for the combination (2.4–6.0) compared to the panitumumab alone (2.2–3.9) ( P = 0.02). Within A375 tumors, the concentration was lower for panitumumab (0.51 μg/g) compared to combination group (0.68 μg/g) ( P = 0.036). Within SKMEL5 tumors, the concentration was lower for panitumumab (0.0.17 μg/g) compared to combination group (0.35 μg/g) ( P = 0.048). Residual tumor (1.0–0.2 mg) could be differentiated from background in both panitumumab and combination groups. For both cell lines, panitumumab and combination groups had greater mean fluorescence of the tumor compared to control IgG. Conclusion The addition of antiangiogenic therapy improves uptake of fluorescently labeled monoclonal antibodies within melanoma tumors. Clinical translation could improve detection of melanoma intraoperatively, reducing positive margins and sparing normal tissue. Level of Evidence NA Laryngoscope , 126:E387–E395, 2016