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首页> 外文期刊>Modern Pathology >High concordance between HercepTest immunohistochemistry and ERBB2 fluorescence in situ hybridization before and after implementation of American Society of Clinical Oncology|[sol]|College of American Pathology 2007 guidelines
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High concordance between HercepTest immunohistochemistry and ERBB2 fluorescence in situ hybridization before and after implementation of American Society of Clinical Oncology|[sol]|College of American Pathology 2007 guidelines

机译:在实施美国临床肿瘤学会前后,HercepTest免疫组织化学与ERBB2荧光原位杂交之间的高度一致性| [溶胶] |美国病理学会2007年指南

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Human epidermal growth factor receptor 2 (HER2, ERBB2) is an important critical predictive marker in patients with invasive breast cancer. It is thus imperative to ensure accuracy and precision in HER2 and ERBB2 testing. In 2007, the American Society of Clinical Oncology and College of American Pathologists (ASCO/CAP) proposed new guidelines for immunohistochemistry and fluorescence in-situ hybridization scoring in an effort to improve accuracy and utility of these companion diagnostic tests. The goal of the 2007 guidelines was to improve concordance rates between the diagnostic tests and decrease the number of inconclusive cases. This study examines the impact in concordance rates and number of inconclusive cases based on the recent change in guidelines in a large study cohort. HER2 immunohistochemistry and ERBB2 fluorescence in-situ hybridization were performed on all specimens from our facility from years 2003 through 2010 (n=1437). Cases from 2003–2007 (n=1016) were scored using Food and Drug Administration guidelines, with immunohistochemical 3+ cases staining >10% of tumor cells and fluorescence in-situ hybridization amplification cutoff value of 2.0. The 2007 guidelines were implemented and scored accordingly for cases from 2008–2010 (n=421), with immunohistochemical 3+ cases staining >30% of tumor cells and fluorescence in-situ hybridization amplification cutoff value of 2.2. We compared concordance rates before and after 2007 guidelines. For the 2003–2007 study population, the concordance rate between the assays was 97.6% with a corresponding kappa coefficient (k) of 0.90. For the 2008–2010 study population, concordance rate was 97.6% with a corresponding k of 0.89. There was no significant difference in number of inconclusive rates before and after 2007 guidelines. In our study, implementation of the new ASCO/CAP 2007 HER2 guidelines did not show a significant difference in concordance rates and did not decrease the number of inconclusive cases.
机译:人表皮生长因子受体2(HER2,ERBB2)是浸润性乳腺癌患者的重要重要预测指标。因此,必须确保HER2和ERBB2测试的准确性和准确性。 2007年,美国临床肿瘤学会和美国病理学家学院(ASCO / CAP)提出了免疫组织化学和荧光原位杂交评分的新指南,以努力提高这些伴随诊断测试的准确性和实用性。 2007年指南的目标是提高诊断测试之间的一致性比率,并减少不确定性案例的数量。这项研究基于大型研究队列中指南的最新变化,研究了一致性率和不确定性案例数的影响。从2003年到2010年,对我们工厂的所有标本进行了HER2免疫组化和ERBB2荧光原位杂交(n = 1437)。根据美国食品药品监督管理局(FDA)的指南,对2003-2007年的病例(n = 1016)进行评分,其中免疫组织化学3+病例的肿瘤细胞染色> 10%,荧光原位杂交扩增的临界值为2.0。实施了2007年指南,并对2008-2010年的病例进行了评分(n = 421),免疫组织化学3+病例染色> 30%的肿瘤细胞,荧光原位杂交扩增临界值为2.2。我们比较了2007年指南之前和之后的一致性比率。对于2003年至2007年的研究人群,分析之间的一致性率为97.6%,相应的卡伯系数(k)为0.90。对于2008-2010年研究人群,一致性率为97.6%,相应的k为0.89。在2007年指南之前和之后的不确定比率数量没有显着差异。在我们的研究中,新ASCO / CAP 2007 HER2指南的实施并未显示出一致性比率有显着差异,也没有减少未结案件的数量。

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