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定义在诊断环境中用于乳腺癌HER-2/neu评估的检测方法。

Defining a test for HER-2/neu evaluation in breast cancer in the diagnostic setting.

作者信息

Hanna W M, Kahn H J, Pienkowska M, Blondal J, Seth A, Marks A

机构信息

Sunnybrook and Women's College Health Sciences CentreDepartments of Pathology, University of Toronto, Toronto, Ontario, Canada.

出版信息

Mod Pathol. 2001 Jul;14(7):677-85. doi: 10.1038/modpathol.3880372.

Abstract

In breast cancer amplification of the HER-2/neu oncogene and over-expression of the protein product is associated with poor prognosis, predicts response to some chemotherapeutic regimens and is the target for Herceptin treatment. To date there are several methods to assess the amplification/over-expression of HER-2/neu with each having advantages and disadvantages. We have studied amplification and over-expression of HER-2/neu in 250 consecutive cases of breast cancer (220 invasive and 30 in situ carcinomas) presenting to the Department of Pathology at Women's College Campus of Sunnybrook and Women's College Health Sciences Center. Thirty percent of the invasive carcinomas were node positive. HER-2/neu protein over-expression was assessed by immunohistochemistry (IH) using antibody CB11 and amplification of the gene by differential PCR. The percentage of tumor cells showing CB11 staining was determined and the most significant cut off point for positivity was > or =10% moderate or strong complete membranous staining. The gene was considered amplified if the density score of the product was > or =2. There was 94% concordance between the two methods (P value.0001). Both methods were positive in 16% of cases and negative in 78% of cases. Discrepant cases were examined by FISH which confirmed the IH results in 9/11 invasive carcinomas. These results show that there is excellent concordance between IH and PCR. However, immunohistochemistry is easier to perform and cheaper than PCR and could be used in routine assessment of HER-2/neu in breast cancer patients.

摘要

在乳腺癌中,HER-2/neu癌基因的扩增及蛋白产物的过表达与预后不良相关,可预测对某些化疗方案的反应,并且是赫赛汀治疗的靶点。迄今为止,有几种方法可用于评估HER-2/neu的扩增/过表达,每种方法都有其优缺点。我们研究了向桑尼布鲁克女子大学校园和女子学院健康科学中心病理科就诊的250例连续乳腺癌病例(220例浸润性癌和30例原位癌)中HER-2/neu的扩增和过表达情况。30%的浸润性癌有淋巴结转移。使用抗体CB11通过免疫组织化学(IH)评估HER-2/neu蛋白的过表达,并通过差异PCR评估基因的扩增情况。确定显示CB11染色的肿瘤细胞百分比,阳性的最显著截断点为≥10%中度或强完全膜染色。如果产物的密度评分≥2,则认为该基因扩增。两种方法之间的一致性为94%(P值0.0001)。两种方法在16%的病例中呈阳性,在78%的病例中呈阴性。对有差异的病例进行荧光原位杂交(FISH)检测,结果在11例浸润性癌中有9例证实了免疫组织化学结果。这些结果表明,免疫组织化学和PCR之间具有良好的一致性。然而,免疫组织化学比PCR更易于操作且成本更低,可用于乳腺癌患者HER-2/neu的常规评估。

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