首页> 外文期刊>The Journal of Pathology: Clinical Research >Fluorescence imaging to localize head and neck squamous cell carcinoma for enhanced pathological assessment
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Fluorescence imaging to localize head and neck squamous cell carcinoma for enhanced pathological assessment

机译:荧光成像定位头颈部鳞状细胞癌,以增强病理评估

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Abstract Accurately identifying close or positive margins in real-time permits re-excision during surgical procedures. Intraoperative assessment of margins via gross examination and frozen section is a widely used tool to assist the surgeon in achieving complete resection. While this methodology permits diagnosis of freshly resected tissue, the process is fraught with misinterpretation and sampling errors. During fluorescence-guided surgery, an exogenous fluorescent agent specific for the target disease is imaged in order to navigate the surgical excision. As this technique quickly advances into the clinic, we hypothesize that the disease-specific fluorescence inherently contained within the resected tissues can be used to guide histopathological assessment. To evaluate the feasibility of fluorescence-guided pathology, we evaluated head and neck squamous cell carcinoma tumour specimens and margins resected from animals and patients after systemic injection of cetuximab-IRDye800CW. In a preclinical model of luciferase-positive tumour resection using bioluminescence as the gold standard, fluorescence assessment determined by closed-field fluorescence imaging of fresh resected margins accurately predicted the presence of disease in 33/39 positive margins yielding an overall sensitivity of 85%, specificity of 95%, positive predictive value (PPV) of 94%, and a negative predictive value (NPV) of 87%, which was superior to both surgical assessment (54%, 61%, 57%, and 58%) and pathological assessment (49%, 95%, 91%, and 66%), respectively. When the power of the technique was evaluated using human-derived tumour tissues, as little as 0.5mg (1mm 3 ) of tumour tissue was identified (tumour-to-background-ratio:5.2). When the sensitivity/specificity of fluorescence-guided pathology was determined using traditional histological assessment as the gold standard in human tissues obtained during fluorescence-guided surgery, the technique was highly accurate with a sensitivity of 91%, specificity of 85%, PPV of 81%, and NPV of 93% for 90 human-derived samples. This approach can be used as a companion to the pathologist, eliminating confounding factors while impacting surgical intervention and patient management.
机译:摘要实时准确识别近缘或正缘可在手术过程中再次切除。通过肉眼检查和冷冻切片术中对切缘的术中评估是一种广泛使用的工具,可协助外科医生完成完全切除。尽管这种方法可以诊断出刚切除的组织,但该过程充满了误解和采样错误。在荧光引导的手术过程中,对目标疾病特有的外源荧光剂进行成像,以指导手术切除。随着这项技术迅速进入临床,我们假设切除的组织内含的疾病特异性荧光可用于指导组织病理学评估。为了评估荧光引导病理学的可行性,我们评估了在全身注射西妥昔单抗-IRDye800CW后从动物和患者中切除的头颈部鳞状细胞癌肿瘤标本和切缘。在以生物发光作为金标准的荧光素酶阳性肿瘤切除的临床前模型中,通过对新鲜切除边缘的封闭视野荧光成像确定的荧光评估准确地预测了33/39阳性边缘中疾病的存在,总体敏感性为85%,特异性为95%,阳性预测值(PPV)为94%,阴性预测值(NPV)为87%,优于手术评估(54%,61%,57%和58%)和病理学评估评估(分别为49%,95%,91%和66%)。当使用人类衍生的肿瘤组织评估该技术的功效时,仅可识别到0.5mg(1mm 3)的肿瘤组织(肿瘤与背景之比:5.2)。当使用传统的组织学评估作为荧光引导手术过程中获得的人体组织的金标准来确定荧光引导病理学的敏感性/特异性时,该技术非常准确,灵敏度为91%,特异性为85%,PPV为81百分比,对于90个人类样本的NPV为93%。这种方法可以用作病理学家的陪伴者,消除混杂因素,同时影响手术干预和患者管理。

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