Characterizing the detection threshold for optical imaging in surgical oncology.

Characterizing the detection threshold for optical imaging in surgical oncology.
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DOI:
10.1002/jso.24733
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发表时间:
2017-12
影响因子:
2.5
通讯作者:
Warram JM
Warram JM
中科院分区:
医学3区
文献类型:
--
作者:
Prince AC;Jani A;Korb M;Tipirneni KE;Kasten BB;Rosenthal EL;Warram JM

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Optical imaging to guide cancer resections is rapidly transitioning into the operating room. However, the sensitivity of this technique to detect subclinical disease is yet characterized. The purpose of this study was to determine the minimum range of cancer cells that can be detected by antibody-based fluorescence imaging. 2LMP (breast), COLO-205 (colon), MiaPaca-2 (pancreas), and SCC-1 (head and neck) cells incubated in vitro with cetuximab-IRDye800CW (dose range 8.6μM to 86nM) were implanted subcutaneously in mice (n=3 mice, 5 tumors/mouse). Following incubation with 8.6×10−2μM of cetuximab-IRDye800CW in vitro, serial dilutions of each cell type (1×103–1×106) were implanted subcutaneously (n=3, 5 tumors/mouse). Tumors were imaged with Pearl Impulse and Xenogen IVIS 100 imaging systems. Scatchard analysis was performed to determine receptor density and kinetics for each cell line. Under conditions of minimal cetuximab-IRDye800CW exposure to low cellular quantity, closed-field fluorescence imaging theoretically detected a minimum of 4.2×104–9.5×104 2LMP cells, 1.9×105–4.5×105 MiaPaca-2 cells, and 2.4×104–6.7×104 SCC-1 cells; COLO-205 cells could not be identified. Higher EGFR-mediated uptake of cetuximab correlated with sensitivity of detection. This study supports the clinical utility of cetuximab-IRDye800CW to sensitively localize subclinical disease in the surgical setting.
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