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多标志物 QPCR 分析检测晚期非小细胞肺癌患者的循环肿瘤细胞。

Circulating tumor cell detection in advanced non-small cell lung cancer patients by multi-marker QPCR analysis.

机构信息

Division of Experimental Therapy, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.

出版信息

Lung Cancer. 2012 Feb;75(2):242-7. doi: 10.1016/j.lungcan.2011.07.003. Epub 2011 Aug 4.

Abstract

BACKGROUND

The aim of this study was to explore circulating tumor cell (CTC) detection in advanced non-small cell lung cancer (NSCLC). CTCs may not only serve as a prognostic marker in selected tumor types, but may also be useful as pharmacodynamic marker in drug development.

METHODS

Fourty-six advanced NSCLC patients and fourty-six healthy controls were included in the study and 8.0 ml of peripheral blood was obtained from each of the participants. Immunomagnetic bead enrichment for cells expressing epithelial cell adhesion molecule (EpCAM) was performed, followed by multi-marker quantitative real-time PCR of a panel of marker genes: cytokeratin 7 (CK7), cytokeratin 19 (CK19), human epithelial glycoprotein (EGP) and fibronectin 1 (FN1). Using quadratic discriminant analysis (QDA), expression values were combined into a single score, which indicated CTC-positivity or -negativity. Test characteristics were assessed using receiver operating characteristic (ROC) curve analysis.

RESULTS

ROC curve analysis showed capability of discrimination between advanced NSCLC patients and healthy controls (area=0.712; 95% CI 0.606-0.819; P<0.001). A cut-off minimizing overall misclassification for QDA-positivity reached a sensitivity of 46% (95% CI 31-61) and a specificity of 93% (95% CI 82-99).

CONCLUSIONS

In this exploratory study, an assay was developed for discriminating CTCs in peripheral blood samples of advanced NSCLC patients from healthy controls. The assay demonstrated an acceptable sensitivity in combination with good specificity. Further validation studies should take place in NSCLC patients and a matched control group.

摘要

背景

本研究旨在探讨循环肿瘤细胞(CTC)在晚期非小细胞肺癌(NSCLC)中的检测。CTC 不仅可以作为某些肿瘤类型的预后标志物,也可能作为药物开发中的药效标志物。

方法

本研究纳入了 46 例晚期 NSCLC 患者和 46 例健康对照者,采集每位参与者 8.0ml 外周血。采用免疫磁珠富集表达上皮细胞黏附分子(EpCAM)的细胞,然后对细胞角蛋白 7(CK7)、细胞角蛋白 19(CK19)、人上皮糖蛋白(EGP)和纤维连接蛋白 1(FN1)等标记基因进行多标记实时定量 PCR。使用二次判别分析(QDA),将表达值组合成一个单一的评分,以指示 CTC 阳性或阴性。使用受试者工作特征(ROC)曲线分析评估测试特征。

结果

ROC 曲线分析显示,该方法能够区分晚期 NSCLC 患者和健康对照者(曲线下面积=0.712;95%CI 0.606-0.819;P<0.001)。为了最小化整体错误分类,QDA 阳性的最佳截断值达到了 46%(95%CI 31-61)的敏感性和 93%(95%CI 82-99)的特异性。

结论

在这项探索性研究中,开发了一种用于区分晚期 NSCLC 患者和健康对照者外周血样本中 CTC 的检测方法。该检测方法具有良好的特异性和可接受的敏感性。应该在 NSCLC 患者和匹配的对照组中进行进一步的验证研究。

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