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首页> 外文期刊>Applied immunohistochemistry and molecular morphology: AIMM >Selecting antibodies to detect HER2 overexpression by immunohistochemistry in invasive mammary carcinomas.
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Selecting antibodies to detect HER2 overexpression by immunohistochemistry in invasive mammary carcinomas.

机译:通过免疫组织化学在浸润性乳腺癌中选择抗体来检测HER2过表达。

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There is an increasing clinical demand for HER2 analysis in breast cancer, especially since the release of trastuzumab. The authors assessed the ability of immunohistochemistry to detect HER2 overexpression in invasive mammary carcinomas (IMC) using five antibodies. Paraffin-embedded samples of 86 IMCs (T2N0) were used to compare the immunohistochemical overexpression of HER2 using two polyclonal antibodies (HercepTest [DAKO] and A0485 [DAKO]) and three monoclonal antibodies (CB11 from two different laboratories, Biogenex and Novocastra, and 4D5 [Genentech]). All immunostainings were scored according to the FDA-approved HercepTest recommendations. The HercepTest-positive cases were compared with gene amplification by FISH (Oncor Inform, Ventana). The HercepTest was positive in 31 of the 86 cases (36.1%). The DAKO antibody A0485 was positive in 25 of the 66 (37.8%). Monoclonal antibody 4D5 was positive in only 15 of the 86 cases (17.4%). There was almost total agreement in results between the two CB11 antibodies: 25 of the 86 positive cases (29.1%). All cases positive for CB11 or 4D5 were HercepTest positive. Most of the HercepTest 2+ cases were negative when using either monoclonal antibody. FISH was positive in 19 of the 20 HercepTest 3+ cases and negative in 5 HercepTest 2+ cases. Three CB11-2+ cases showed no amplification by FISH. In three FISH-positive cases the immunohistochemistry showed no overexpression by all antibodies used. These findings suggest that immunohistochemistry may be used reliably as a primary methodology for evaluating HER2; however, the use of polyclonal antibodies may not be adequate to assess HER2 overexpression. CB11, regardless of the manufacturer (Biogenex or Novocastra), showed better concordance with FISH (kappa=0.83) than did the polyclonal antibodies.
机译:乳腺癌中HER2分析的临床需求不断增长,尤其是自曲妥珠单抗释放以来。作者使用五种抗体评估了免疫组织化学检测浸润性乳腺癌(IMC)中HER2过表达的能力。使用86种IMC(T2N0)的石蜡包埋样品,使用两种多克隆抗体(HercepTest [DAKO]和A0485 [DAKO])和三种单克隆抗体(来自两个不同实验室Biogenex和Novocastra的CB11)比较HER2的免疫组织化学过表达。 4D5 [Genentech])。所有的免疫染色均根据FDA批准的HercepTest建议进行评分。将HercepTest阳性病例与通过FISH(Oncor Inform,Ventana)进行的基因扩增进行比较。 HercepTest在86例病例中有31例呈阳性(36.1%)。 DAKO抗体A0485在66的25(37.8%)中呈阳性。 86例中只有15例(17.4%)的单克隆抗体4D5呈阳性。两种CB11抗体之间的结果几乎完全一致:86例阳性病例中有25例(29.1%)。所有CB11或4D5阳性的病例均为HercepTest阳性。使用任一单克隆抗体时,大多数HercepTest 2+病例均为阴性。在20例HercepTest 3+病例中,有19例FISH阳性,在5例HercepTest 2+病例中,FISH阴性。 3例CB11-2 +病例未通过FISH扩增。在三种FISH阳性病例中,免疫组织化学显示所有使用的抗体均未过度表达。这些发现表明,免疫组化可以可靠地用作评估HER2的主要方法。但是,使用多克隆抗体可能不足以评估HER2过表达。不管生产商是什么(Biogenex或Novocastra),CB11与多克隆抗体相比,与FISH的一致性更好(kappa = 0.83)。

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