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[乳腺癌中的ErbB2诊断——最新进展]

[ErbB2 diagnostics in breast cancer--an update].

作者信息

Rüschoff J, Nagelmeier I, Hofmann M, Henkel Th, Stoss O

机构信息

Pathologie Nordhessen, Kassel, Deutschland.

出版信息

Pathologe. 2009 Mar;30(2):147-55. doi: 10.1007/s00292-009-1126-3.

DOI:10.1007/s00292-009-1126-3
PMID:19214513
Abstract

Determining ErbB2/Her-2/neu status has become an essential part of breast cancer diagnosis and a prerequisite before considering a patient's eligibility for treatment with trastuzumab. Currently the most common techniques to assess ErbB2 status in routine practice are the identification of receptor overexpression by means of immunohistochemistry (IHC) and the analysis of gene amplification by means of dual color fluorescence in situ hybridisation (FISH). According to recent recommendations ("ASCO/CAP Guidelines" and German S3 guidelines for breast cancer) the choice of primary test procedure--IHC or ISH - is left to the individual institution. Both techniques are of equal predictive value provided that strict quality precautions have been taken: internal test validation by comparing IHC and (F)ISH, carrying out controls, and annual participation in round-robin tests. Equivocal IHC (score 2+) has to be checked by ISH for amplification. Borderline ISH (ratio 1.8-2.2 or gene copy number 4.0-6.0) should be retested by counting additional cells or performing IHC. In approximately 5% of cases these criteria give conflicting results and the gene copy number alone generates over 90% of the equivocal ISH cases, mostly due to chromosome 17 polysomy. These cases need to be tested by IHC since over-expression is very exceptional and only these tumors have the potential to be trastuzumab responders.

摘要

确定ErbB2/Her-2/neu状态已成为乳腺癌诊断的重要组成部分,也是考虑患者是否适合接受曲妥珠单抗治疗的前提条件。目前,在常规实践中评估ErbB2状态最常用的技术是通过免疫组织化学(IHC)鉴定受体过表达,以及通过双色荧光原位杂交(FISH)分析基因扩增。根据最近的建议(“美国临床肿瘤学会/美国病理学家协会指南”和德国乳腺癌S3指南),主要检测方法(IHC或ISH)的选择由各机构自行决定。只要采取了严格的质量预防措施,这两种技术具有同等的预测价值:通过比较IHC和(F)ISH进行内部检测验证、进行对照以及每年参与轮测。IHC结果不明确(评分2+)必须通过ISH检测扩增情况。ISH结果处于临界值(比率1.8 - 2.2或基因拷贝数4.0 - 6.0)时,应通过计数更多细胞或进行IHC重新检测。在大约5%的病例中,这些标准会给出相互矛盾的结果,仅基因拷贝数就导致超过90%的ISH结果不明确病例,主要原因是17号染色体多体性。这些病例需要通过IHC检测,因为过表达非常罕见,只有这些肿瘤有可能对曲妥珠单抗产生反应。

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Br J Cancer. 2012 Mar 13;106(6):1033-8. doi: 10.1038/bjc.2012.18. Epub 2012 Feb 28.
2
[Intratumoral heterogeneity of HER2 status in breast carcinoma].[乳腺癌中HER2状态的肿瘤内异质性]
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本文引用的文献

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Disease-free survival according to degree of HER2 amplification for patients treated with adjuvant chemotherapy with or without 1 year of trastuzumab: the HERA Trial.HERA试验:接受或不接受1年曲妥珠单抗辅助化疗的患者,根据HER2扩增程度的无病生存率
J Clin Oncol. 2009 Jun 20;27(18):2962-9. doi: 10.1200/JCO.2008.19.7939. Epub 2009 Apr 13.
2
Prediction of HER2 gene status in Her2 2+ invasive breast cancer: a study of 108 cases comparing ASCO/CAP and FDA recommendations.人表皮生长因子受体2(HER2)2+浸润性乳腺癌中HER2基因状态的预测:一项比较美国临床肿瘤学会(ASCO)/美国病理学家学会(CAP)和美国食品药品监督管理局(FDA)建议的108例病例研究
Mod Pathol. 2009 Mar;22(3):403-9. doi: 10.1038/modpathol.2008.195. Epub 2008 Dec 5.
3
HER-2 gene amplification, HER-2 and epidermal growth factor receptor mRNA and protein expression, and lapatinib efficacy in women with metastatic breast cancer.
HER-2基因扩增、HER-2和表皮生长因子受体的mRNA及蛋白表达,以及拉帕替尼在转移性乳腺癌女性患者中的疗效
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What causes discrepancies in HER2 testing for breast cancer? A Japanese ring study in conjunction with the global standard.乳腺癌HER2检测结果出现差异的原因是什么?一项与全球标准相结合的日本环式研究。
Am J Clin Pathol. 2008 Dec;130(6):883-91. doi: 10.1309/AJCP5UUMFMA5ZKII.
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Targeted therapies and biological modifiers. Introduction.靶向治疗与生物修饰剂。引言。
Semin Diagn Pathol. 2008 Nov;25(4):231.
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Proficiency testing of immunohistochemical biomarker assays in breast cancer.乳腺癌免疫组化生物标志物检测的能力验证
Virchows Arch. 2008 Dec;453(6):537-43. doi: 10.1007/s00428-008-0688-4. Epub 2008 Oct 29.
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