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INTRAOPERATIVE DETECTION OF LYMPH NODE MICROMETASTASIS USING A RAPID IMMUNOHISTOCHEMICAL STAINING METHOD IN NON-SMALL CELL LUNG CANCER

机译:非小细胞肺癌快速免疫组织化学染色术中术中淋巴结微转移的检测

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摘要

Nodal micrometastasis in non-small cell lung cancer (NSCLC) is associated with a poorer survival rate than node-negative disease. Furthermore, lymph node micrometastasis often cannot be detected using conventional hematoxylin and eosin staining of frozen sections ; detection requires additional time-consuming immunohistochemical (IHC) analysis of paraffin-embedded tissue. We previously developed and reported a device that enables us to complete IHC analyses within 11 minutes. In the present study, we used this rapid-IHC protocol with an anti-cytokeratin antibody and analyzed 205 mediastinal lymph nodes dissected during surgery for NSCLC. Although we modified the original rapid-IHC procedure to block endogenous peroxidase activity, which could potentially cause misdiagnosis, the staining was still completed within 19 min. On the basis of conventional histological examination, 7 lymph nodes from 3 patients were deemed positive for micrometastasis. By contrast using hematoxylin and eosin staining, 13 lymph nodes from 7 patients were diagnosed positive on the basis of cytokeratin-detection using routine-IHC, and the same 13 nodes were diagnosed positive on the basis of rapid-IHC. That is, all nodes deemed positive with the routine-IHC procedure were also positive with the rapid-IHC procedure. Assuming the results of the routine-IHC are correct, the sensitivity, specificity and accuracy of rapid-IHC are 100%, 100% and 100%, respectively. These findings demonstrate the utility of our rapid-IHC analysis for intraoperative diagnosis of micrometastasis. However, our findings are limited by the fact that we tested the method using a single antibody at a single institute. Further investigation in multicenter studies will be needed to confirm the utility of this method.
机译:非小细胞肺癌(NSCLC)的淋巴结微转移与淋巴结阴性者相比,生存率较差。此外,使用常规苏木精和曙红对冰冻切片进行染色通常无法检测到淋巴结微转移;检测需要对石蜡包埋的组织进行其他耗时的免疫组织化学(IHC)分析。我们之前开发并报告了一种设备,该设备使我们能够在11分钟内完成IHC分析。在本研究中,我们将这种快速IHC方案与抗细胞角蛋白抗体一起使用,并分析了NSCLC手术期间解剖的205个纵隔淋巴结。尽管我们修改了最初的快速IHC程序以阻止可能引起误诊的内源性过氧化物酶活性,但染色仍在19分钟内完成。根据常规组织学检查,将3例患者的7个淋巴结微转移视为阳性。相比之下,使用苏木精和曙红染色,根据常规IHC对细胞角蛋白的检测,将7例患者的13个淋巴结诊断为阳性,而根据快速IHC,将13例淋巴结诊断为阳性。也就是说,在常规IHC程序中被认为是阳性的所有节点在快速IHC程序中也都是阳性。假设常规IHC的结果正确,快速IHC的敏感性,特异性和准确性分别为100%,100%和100%。这些发现证明了我们的快速IHC分析在术中诊断微转移中的实用性。但是,我们的发现受到以下事实的限制:我们在单个机构中使用单一抗体测试了该方法。需要在多中心研究中进行进一步研究,以确认该方法的实用性。

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