Baik Fred M, Hansen Stacey, Knoblaugh Sue E, Sahetya Disha, Mitchell Ryan M, Xu Chang, Olson James M, Parrish-Novak Julia, Méndez Eduardo
Department of Otolaryngology-Head and Neck Surgery, University of Washington, Seattle.
Blaze Bioscience Inc, Seattle, Washington.
JAMA Otolaryngol Head Neck Surg. 2016 Apr;142(4):330-8. doi: 10.1001/jamaoto.2015.3617.
Surgical cure of head and neck squamous cell carcinoma (HNSCC) remains hampered by inadequately resected tumors and poor recognition of lesions with malignant potential. BLZ-100 is a chlorotoxin-based, tumor-targeting agent that has not yet been studied in HNSCC.
To evaluate BLZ-100 uptake in models of HNSCC and oral dysplasia.
DESIGN, SETTING, AND PARTICIPANTS: This was an observational study (including sensitivity and specificity analysis) of BLZ-100 uptake in an orthotopic xenograft mouse model of HNSCC and a carcinogen-induced dysplasia model of hamster cheek pouches.
Various HNSCC xenografts were established in the tongues of NOD-scid IL2Rgammanull (NSG) mice. BLZ-100 was intravenously injected and fluorescence uptake was measured. To induce dysplasia, the carcinogen 7,12-dimethylbenz(a)anthracene (DMBA) was applied to the cheek pouch of Golden Syrian hamsters for 9 to16 weeks. BLZ-100 was subcutaneously injected, and fluorescence uptake was measured.
The signal-to-background ratio (SBR) of BLZ-100 was measured in tumor xenografts. To calculate the sensitivity and specificity of BLZ-100 uptake, a digital grid was placed over tissue sections and correlative histologic sections to discretely measure fluorescence intensity and presence of tumor; a receiver operating characteristic (ROC) curve was then plotted. In the hamster dysplasia model, cheeks were graded according to dysplasia severity. The SBR of BLZ-100 was compared among dysplasia grades.
In HNSCC xenografts, BLZ-100 demonstrated a mean (SD) SBR of 2.51 (0.47). The ROC curve demonstrated an area under the curve (AUC) of 0.89; an SBR of 2.50 corresponded to 92% sensitivity and 74% specificity. When this analysis was focused on the tumor and nontumor interface, the AUC increased to 0.97; an SBR of 2.50 corresponded to 95% sensitivity and 91% specificity. DMBA treatment of hamster cheek pouches generated lesions representing all grades of dysplasia. The SBR of high-grade dysplasia was significantly greater than that of mild-to-moderate dysplasia (2.31 [0.71] vs 1.51 [0.34], P = .006).
BLZ-100 is a sensitive and specific marker of HNSCC and can distinguish high-risk from low-risk dysplasia. BLZ-100 has the potential to serve as an intraoperative guide for tumor margin excision and identification of premalignant lesions.
头颈部鳞状细胞癌(HNSCC)的手术治愈仍受到肿瘤切除不充分以及对具有恶性潜能病变识别不足的阻碍。BLZ - 100是一种基于氯毒素的肿瘤靶向剂,尚未在HNSCC中进行研究。
评估BLZ - 100在HNSCC和口腔发育异常模型中的摄取情况。
设计、设置和参与者:这是一项关于BLZ - 100在HNSCC原位异种移植小鼠模型和致癌物诱导的仓鼠颊囊发育异常模型中摄取情况的观察性研究(包括敏感性和特异性分析)。
在NOD - scid IL2Rγnull(NSG)小鼠的舌部建立各种HNSCC异种移植瘤。静脉注射BLZ - 100并测量荧光摄取。为诱导发育异常,将致癌物7,12 - 二甲基苯并(a)蒽(DMBA)应用于金黄叙利亚仓鼠的颊囊9至16周。皮下注射BLZ - 100并测量荧光摄取。
在肿瘤异种移植瘤中测量BLZ - 100的信号与背景比(SBR)。为计算BLZ - 100摄取的敏感性和特异性,在组织切片和相关组织学切片上放置数字网格以离散测量荧光强度和肿瘤的存在;然后绘制受试者操作特征(ROC)曲线。在仓鼠发育异常模型中,根据发育异常严重程度对颊部进行分级。比较不同发育异常等级之间BLZ - 100的SBR。
在HNSCC异种移植瘤中,BLZ - 100的平均(标准差)SBR为2.51(0.47)。ROC曲线显示曲线下面积(AUC)为0.89;SBR为2.50时对应92%的敏感性和74%的特异性。当该分析聚焦于肿瘤与非肿瘤界面时,AUC增加到0.97;SBR为2.50时对应95%的敏感性和91%的特异性。用DMBA处理仓鼠颊囊产生了代表所有发育异常等级的病变。高级别发育异常的SBR显著高于轻度至中度发育异常(2.31 [0.71]对1.51 [0.34],P = 0.006)。
BLZ - 100是HNSCC的一种敏感且特异的标志物,能够区分高风险和低风险的发育异常。BLZ - 100有潜力作为肿瘤边缘切除和癌前病变识别的术中指导。