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首页> 外文期刊>Human Pathology >Breast cancers with a HER2/CEP17 ratio of 2.0 or greater and an average HER2 copy number of less than 4.0 per cell: frequency, immunohistochemical correlation, and clinicopathological features
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Breast cancers with a HER2/CEP17 ratio of 2.0 or greater and an average HER2 copy number of less than 4.0 per cell: frequency, immunohistochemical correlation, and clinicopathological features

机译:HER2 / CEP17比率为2.0或更大的乳腺癌,平均HER2拷贝数小于每种细胞的4.0:频率,免疫组织化学相关性和临床病理特征

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The 2013 American Society of Clinical Oncology and College of American Pathologists (ASCO/CAP) guidelines classified breast cancers with a fluorescence in situ hybridization dual-probe HER2/CEP17 ratio of 2 or greater as "amplified," inclusive of cases with a HER2 copy number less than 4. The 2018 ASCO/CAP update assigns HER2/neu status for the latter group in a fashion that is highly dependent on the associated immunohistochemical findings. Herein, the authors define the frequency, immunohistochemical correlates, and other clinicopathological features of breast cancers with HER2/CEP17 ratio of 2 or greater and HER2/neu copy number less than 4 (group A), based on an analysis of an institutional cohort assessed for HER2/neu status by both florescence in situ hybridization and immunohistochemistry and scored using 2013 ASCO/CAP criteria. Group A cases were compared with a group B of HER2/neu-amplified breast cancers with a HER2/neu copy number of 4 or greater regarding a variety of clinicopathological features. One hundred sixty-nine (14%) of 1201 cases were HER2/neu amplified, 18 (10.7%) in group A and 151 (89.3%) in group B. By immunohistochemistry, 61.1% of group A cases were HER2/neu negative, 7 (38.9%) were equivocal, and none were positive. In contrast, 66.9% of group B cases were HER2 positive (3+). We could not demonstrate statistically significant differences between the 2 groups regarding standard clinicopathological variables. In summary, our group A cases account for 1.5% of breast cancers, and 10.7% of all HER2/neu-amplified cancers classified as such based on 2013 ASCO/CAP criteria. They are predominantly HER2/neu negative by immunohistochemistry, which suggests that they are biologically different from classically HER2/neu-amplified cases and which validates the 2018 ASCO/CAP guideline against automatically classifying such cases as HER2/neu amplified. (C) 2018 Elsevier Inc. All rights reserved.
机译:2013年美国临床肿瘤学会和美国病理学家(ASCO / CAP)指南分类为乳腺癌,荧光原位杂交双探针HER2 / CEP17比例为2或更高,如“扩增”,包括HER2副本的病例小于4. 2018年ASCO / CAP更新以高度依赖于相关免疫组织化学发现的方式为后者组分配HER2 / NEU状态。在此,基于评估制度队列的分析通过繁殖和免疫组织化学的繁殖和免疫组化的繁殖和免疫组化,使用2013年ASCO / CAP标准进行繁殖。将病例与HER2 / Neu-SAMADIZED乳腺癌B组进行比较,其具有HER2 / NEU拷贝数4或更大的关于各种临床病理特征。 1201例(14%)的1201例(14%)是HER2 / Neu扩增,18(10.7%)在B组,B组中的151(89.3%)。通过免疫组织化学,61.1%的病例是HER2 / NEU负数,7(38.9%)等于圆锥,没有阳性。相比之下,B组患者的66.9%是HER2阳性(3+)。我们无法在标准临床病理变量之间展示2组之间的统计学意义。总之,我们的案例占1.5%的乳腺癌,占所有HER2 / NEU扩增的癌症的10.7%,如2013年ASCO / CAP标准。它们主要由免疫组织化学主要是HER2 / NEU,这表明它们与经典的MER2 / NEU放大的病例产生了生物学不同,并且验证了2018年ASCO / CAP指南,因为HER2 / NEU扩增自动分类此类病例。 (c)2018年Elsevier Inc.保留所有权利。

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