Department of Otolaryngology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Clin Cancer Res. 2011 Apr 1;17(7):1858-66. doi: 10.1158/1078-0432.CCR-10-3110. Epub 2011 Feb 25.
Sentinel node biopsy (SNB) has been shown to accurately stage the regional lymphatics in oral carcinoma. However, intraoperative pathology is only moderately sensitive and final pathology takes several days to complete. The purpose of this study was to develop a rapid, automated, and quantitative real-time PCR (qRT-PCR) assay that can match final pathology in an intraoperative time frame.
Four hundred forty-eight grossly tumor-negative lymph nodes were evaluated for expression of 3 markers [PVA (pemphigus vulgaris antigen), PTHrP (parathyroid hormone-related protein), and TACSTD1 (tumor-associated calcium signal transducer 1)]. Conformity of metastasis detection by qRT-PCR was determined using hematoxylin and eosin and immunohistochemistry staining as the gold standard. PVA and TACSTD1 were then multiplexed with β-glucuronidase to develop a rapid, automated single-tube qRT-PCR assay using the Cepheid GeneXpert system. This assay was used to analyze 103 lymph nodes in an intraoperative time frame.
Four hundred forty-two nodes produced an informative result for both qRT-PCR and pathologic examination. Concordance of qRT-PCR for individual markers with final pathology ranged from 93% to 98%. The best marker combination was TACSTD1 and PVA. A rapid, multiplex assay for TACSTD1 and PVA was developed on the Cepheid GeneXpert and demonstrated an excellent reproducibility and linearity. Analysis of 103 lymph nodes demonstrated 94.2% accuracy of this assay for identifying positive and negative nodes. The average time for each assay to yield results was 35 minutes.
A rapid, automated qRT-PCR assay can detect lymph node metastasis in head and neck cancer with high accuracy compared to pathologic analysis and may be more accurate than intraoperative pathology. Combined, SNB and rapid qRT-PCR could more appropriately guide surgical treatment of patients with head and neck cancer.
前哨淋巴结活检 (SNB) 已被证明可准确分期口腔癌的区域淋巴结。然而,术中病理检查的敏感性仅为中等,且最终病理检查需要数天才能完成。本研究旨在开发一种快速、自动化和定量实时 PCR (qRT-PCR) 检测方法,以便在术中时间内与最终病理相匹配。
评估了 448 个大体上肿瘤阴性的淋巴结,以评估 3 种标志物 [PVA(寻常性天疱疮抗原)、PTHrP(甲状旁腺激素相关蛋白)和 TACSTD1(肿瘤相关钙信号转导蛋白 1)] 的表达。使用苏木精和伊红以及免疫组织化学染色作为金标准,确定 qRT-PCR 检测转移的一致性。然后,将 PVA 和 TACSTD1 与β-葡糖苷酸酶进行多重化,以开发一种快速、自动化的单管 qRT-PCR 检测方法,该方法使用 Cepheid GeneXpert 系统进行分析。该检测方法用于分析 103 个术中时间的淋巴结。
442 个淋巴结的 qRT-PCR 和病理检查均产生了有意义的结果。单个标志物的 qRT-PCR 与最终病理的一致性范围为 93%至 98%。最佳标志物组合是 TACSTD1 和 PVA。在 Cepheid GeneXpert 上开发了用于 TACSTD1 和 PVA 的快速多重检测方法,该方法显示出极好的重现性和线性。对 103 个淋巴结的分析表明,该检测方法对识别阳性和阴性淋巴结的准确率为 94.2%。每个检测的平均时间为 35 分钟。
与病理分析相比,快速、自动化的 qRT-PCR 检测方法可对头颈部癌症的淋巴结转移进行高精度检测,其准确性可能高于术中病理检查。SNB 和快速 qRT-PCR 的联合应用可以更恰当地指导头颈部癌症患者的手术治疗。