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HER2eu, Topoisomerase 2a, Estrogen and Progesterone Receptors: Discordance between Primary Breast Cancer and Metastatic Axillary Lymph Node in Expression and Amplification Characteristics

机译:HER2 / neu,拓扑异构酶2a,雌激素和孕激素受体:原发性乳腺癌和转移性腋窝淋巴结表达和扩增特征之间的不一致。

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Molecular classification of breast cancer (BC) and the evaluation of new biological markers such as estrogen receptor (ER), progesterone receptor (PR), ErbB2 (HER2) and topoisomerase 2a (Topo2a) status are claimed to be important parameters in the management of BC therapy. In case of heterogeneity between primary BC and metastatic site, this implies profound limitations of efficient systemic therapy. Therefore, it is essential to analyze whether biological markers of BC relate to identical expression profiles of metastatic lymph nodes (mLNs). We used paraffin-embedded tumor tissue from 119 patients with at least 1 mLN. Immunohistochemistry (IHC) was used to analyze ER, PR, HER2 and Topo2a. In addition, HER2 and Topo2a amplification was evaluated by fluorescence/chromogenic in situ hybridization (FISH/CISH) in all samples with a HER2 score of 2+/3+ by IHC. Overall, the percentage of discordant marker status in the BC and its mLN was 2.6% for ER, 3.5% for PR, 3.4% for HER2, and 3.4% for Topo2a. With FISH/CISH, the amplification rate for Topo2a and HER2 was concordant in all cases. Because there are no prospective studies, it remains unclear whether these discrepancies have an effect on patient survival.
机译:据称乳腺癌的分子分类(BC)和评估新的生物标记物,如雌激素受体(ER),孕激素受体(PR),ErbB2(HER2)和拓扑异构酶2a(Topo2a)的状态,是控制乳腺癌的重要参数。 BC疗法。如果原发性BC和转移部位之间存在异质性,则意味着有效的全身治疗的局限性。因此,分析BC的生物学标记是否与转移性淋巴结(mLNs)的相同表达谱相关至关重要。我们使用了来自119例至少1 mLN的石蜡包埋的肿瘤组织。免疫组织化学(IHC)用于分析ER,PR,HER2和Topo2a。另外,通过IHC对所有HER2得分为2 + / 3 +的样品进行荧光/发色原位杂交(FISH / CISH)评估了HER2和Topo2a扩增。总体而言,在BC及其mLN中,ER的不一致性标记状态百分比为2.6%,PR的为3.5%,HER2的为3.4%,Topo2a的为3.4%。使用FISH / CISH,Topo2a和HER2的扩增率在所有情况下都是一致的。由于尚无前瞻性研究,因此尚不清楚这些差异是否会影响患者生存。

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