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晚期胃癌和胃食管交界处癌的 HER2 检测:一项全澳检测计划分析。

HER2 testing in advanced gastric and gastro-oesophageal cancer: analysis of an Australia-wide testing program.

机构信息

PathWest, QEII Medical Centre and School of Pathology & Laboratory Medicine, University of Western Australia, Perth, WA, Australia.

SydPath, St Vincent's Hospital, Sydney, NSW, Australia.

出版信息

Pathology. 2017 Oct;49(6):575-581. doi: 10.1016/j.pathol.2017.05.009. Epub 2017 Aug 18.

Abstract

This Australian human epidermal growth factor receptor 2 (HER2) testing program aimed to analyse >800 cases tested in a coordinated setting to further evaluate the criteria to establish HER2 status in advanced gastric and gastro-oesophageal junction (GOJ) cancer. Heterogeneity, and minimum number of biopsy fragments for reliable HER2 assessment were also examined in a subset of samples. Five laboratories tested 891 samples referred to determine HER2 status for potential anti-HER2 treatment. Cancer site, specimen type (endoscopic biopsy/resection/metastases), immunohistochemistry (IHC) score, HER2 gene and CEP17 copy number (CN) and HER2:CEP17 ratios were recorded. Samples were derived from stomach (53.1%), GOJ (28.2%) or metastases (18.5%). IHC for HER2 and dual probe HER2:CEP17 in situ hybridisation (ISH) were performed in parallel. A stringent definition (SD) of HER2 positivity was used (IHC2+/3+ plus CN>6 and ratio>2) and compared with other published criteria. HER2 positive rate was 13.9% (114/820) by SD, and 12.9-16.0% using other definitions. There was higher concordance between IHC and HER2 CN by ISH than with ratio. The HER2 positive rate was significantly higher in GOJ samples than others (p = 0.03) and in endoscopic biopsies than resections (p = 0.047). In a subset of 98 positive cases, 39 (39.8%) showed heterogeneity, and in 282 endoscopic biopsies positivity rate plateaued at five tumour fragments, suggesting this is the minimum number of biopsies that should be examined.

摘要

这项澳大利亚人类表皮生长因子受体 2(HER2)检测计划旨在分析 800 多例在协调环境下检测的病例,以进一步评估在晚期胃癌和胃食管交界处(GOJ)癌症中建立 HER2 状态的标准。还在部分样本中检查了异质性和可靠评估 HER2 所需的最小活检片段数量。五个实验室测试了 891 个样本,以确定潜在抗 HER2 治疗的 HER2 状态。记录了癌症部位、标本类型(内镜活检/切除/转移)、免疫组织化学(IHC)评分、HER2 基因和 CEP17 拷贝数(CN)以及 HER2:CEP17 比值。样本来源于胃(53.1%)、GOJ(28.2%)或转移(18.5%)。平行进行了 HER2 的 IHC 和双重探针 HER2:CEP17 原位杂交(ISH)。采用严格的 HER2 阳性定义(SD)(IHC2+/3+加上 CN>6 和比值>2),并与其他已发表的标准进行了比较。根据 SD,HER2 阳性率为 13.9%(114/820),而根据其他定义为 12.9-16.0%。IHC 与 HER2 CN 的一致性高于与比值的一致性。GOJ 样本的 HER2 阳性率明显高于其他样本(p=0.03),内镜活检的阳性率高于切除(p=0.047)。在 98 例阳性病例的亚组中,39 例(39.8%)显示异质性,在 282 例内镜活检中,阳性率在 5 个肿瘤片段时达到平台期,表明这是应检查的最小活检数量。

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