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采用分子亚型对乳腺癌进行分类时,前哨淋巴结的定量分子分析可能有助于预测腋窝淋巴结的状态。

Quantitative molecular analysis of sentinel lymph node may be predictive of axillary node status in breast cancer classified by molecular subtypes.

机构信息

Department of Pathology, Regina Elena National Cancer Institute, Rome, Italy.

出版信息

PLoS One. 2013;8(3):e58823. doi: 10.1371/journal.pone.0058823. Epub 2013 Mar 22.

Abstract

To determine the performance of intraoperative one-step nucleic acid amplification (OSNA) assay in detecting sentinel lymph node metastases compared to postoperative histology taking into account breast cancer molecular classification and to evaluate whether the level of cytokeratin 19 mRNA copy number may be useful in predicting the likelihood of a positive axillary lymph node dissection. OSNA assay was performed in a prospective series of 903 consecutive sentinel lymph nodes from 709 breast cancer patients using 2 alternate slices of each sentinel lymph node. The remaining 2 slices were investigated by histology. Cytokeratin 19 mRNA copy number, which distinguishes negative cases (<250 copies), micrometastases (+, ≥250≤5000 copies) and macrometastases (++, >5000 copies), was compared to axillary lymph node dissection status and to the biological tumor profile. Concordance between OSNA and histopathology was 95%, specificity 95% and sensitivity 93%. Multiple Corresponce Analysis and logistic regression evidenced that positive axillary lymph node dissection was significantly associated with a higher cytokeratin 19 mRNA copy number (>5000; p<0.0001), HER2 subtype (p = 0.007) and lymphovascular invasion (p<0.0001). Conversely, breast cancer patients with cytokeratin 19 mRNA copy number <2000 mostly presented a luminal subtype and a negative axillary lymph node dissection. We confirmed that OSNA assay can provide standardized and reproducible results and that it represents a fast and quantitative tool for intraoperative evaluation of sentinel lymph node. Omission of axillary lymph node dissection could be proposed in patients presenting a sentinel lymph node with a cytokeratin 19 mRNA copy number <2000 and a Luminal tumor phenotype.

摘要

为了确定术中一步法核酸扩增(OSNA)检测在检测前哨淋巴结转移方面的性能,与术后组织学相比,同时考虑乳腺癌分子分类,并评估细胞角蛋白 19 mRNA 拷贝数的水平是否可用于预测阳性腋窝淋巴结清扫术的可能性。使用每个前哨淋巴结的 2 个替代切片,对 709 例乳腺癌患者的 903 个连续前哨淋巴结进行了前瞻性系列 OSNA 检测。其余 2 个切片进行组织学检查。细胞角蛋白 19 mRNA 拷贝数(区分阴性病例(<250 拷贝)、微转移(+,≥250≤5000 拷贝)和宏转移(++,>5000 拷贝))与腋窝淋巴结清扫状态和生物学肿瘤特征进行了比较。OSNA 与组织病理学的一致性为 95%,特异性为 95%,敏感性为 93%。多元对应分析和逻辑回归表明,阳性腋窝淋巴结清扫与较高的细胞角蛋白 19 mRNA 拷贝数(>5000;p<0.0001)、HER2 亚型(p=0.007)和淋巴管侵犯(p<0.0001)显著相关。相反,细胞角蛋白 19 mRNA 拷贝数<2000 的乳腺癌患者主要表现为腔型亚型和阴性腋窝淋巴结清扫。我们证实 OSNA 检测可提供标准化和可重复的结果,并且它代表了一种用于术中评估前哨淋巴结的快速定量工具。对于细胞角蛋白 19 mRNA 拷贝数<2000 且存在腔型肿瘤表型的前哨淋巴结患者,可以考虑省略腋窝淋巴结清扫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b64c/3606361/159d27d2ed7d/pone.0058823.g001.jpg

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