原发性男性乳腺癌中的 HER2 低表达。

IF 3.3 4区 医学 Q2 ONCOLOGY Breast Cancer : Targets and Therapy Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI:10.2147/BCTT.S450682
Katleen Nobbe, Melanie Erices-Leclercq, Frank Foerster, Robert Förster, Stephan E Baldus, Christian Rudlowski, Lars Schröder, Sabine Lubig
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引用次数: 0

摘要

目的:HER2 靶向抗体药物共轭物(ADC)的问世为表达低水平 HER2(HER2 低)的女性乳腺癌患者(FBC)提供了新的治疗选择。目前还没有证据表明 HER2 低表达是一种新的 FBC 亚型。目前还缺乏确定 HER2 低水平对男性乳腺癌(MBC)影响的研究。在本研究中,我们评估了原发性 MBC 中 HER2 低的流行率,并将结果与患者特征相关联:在这项研究中,我们从 1995 年至 2022 年期间在德国贝吉施格拉德巴赫、开姆尼茨和茨维考的乳腺癌科诊断和治疗原发性浸润性乳腺癌的 120 名男性患者身上获取了组织学标本。HER2 免疫染色和原位杂交由中心病理科进行,并根据 ASCO/CAP 指南进行评估。研究了HER2低表达与肿瘤生物学特征和患者预后的相关性:在所有病例中,4 例患者(3.3%)HER2 阳性(3+),39 例患者(32.5%)HER2 低表达,7 例患者(5.8%)HER2 2+(无扩增),32 例患者(26.7%)HER2 1+,77 例患者(64.2%)HER2 零表达。在 77 个 HER2 为零的病例中,47 个肿瘤(61.0%)显示为不完全染色,结论是:我们的研究结果表明,在原发性 MBC 中,HER2 低表达的发生率明显较低。然而,HER2 低表达的肿瘤并未显示出特定的肿瘤生物学特征,因此无法定义 MBC 中的一种新的乳腺癌亚型。我们的研究结果表明,大量的 MBC 患者可以从 ADCs 中获益,就像在 FBC 中显示的那样。要更好地了解HER2低表达乳腺癌(包括一般乳腺癌和MBC),还需要进一步的研究。
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HER2 Low Expression in Primary Male Breast Cancer.

Purpose: The introduction of HER2-targeting antibody drug conjugates (ADCs) offers new treatment options for female breast cancer patients (FBC) expressing low levels of HER2 (HER2 low). No evidence was found that HER2 low describes a new FBC subtype. There is a lack of studies determining the impact of HER2 low in male breast cancer (MBC). In this study, we evaluate the prevalence of HER2 low in primary MBC and correlate the results with patient characteristics.

Patients and methods: In this study, histological specimens were obtained from 120 male patients diagnosed and treated for primary invasive breast cancer from 1995 to 2022 at Breast Cancer Units in Bergisch Gladbach, Chemnitz, and Zwickau, Germany. HER2 immunostaining and in situ hybridization were performed by central pathology and evaluated based on the ASCO/CAP guidelines. The correlation of expression of HER2 low with tumor biological characteristics and patient outcomes was investigated.

Results: Out of all cases, four patients (3.3%) showed HER2 positivity (3+), 39 (32.5%) patients were classified as HER2 low, 7 (5.8%) were HER2 2+ (no amplification), 32 (26.7%) were HER2 1+, and 77 (64.2%) were classified as HER2 zero. Out of 77 HER2 zero cases, 47 tumors (61.0%) showed incomplete staining, with <10% of tumor cells classified as HER2 ultralow. No statistical correlation between HER2 low and tumor biological characteristics and patients' survival was found.

Conclusion: Our findings show a notable, albeit lower, prevalence of HER2 low expression in primary MBC. However, tumors expressing HER2 low do not show specific tumor biological features to define a new breast cancer subtype in MBC. Our results suggest that a significant number of MBC patients could benefit from ADCs, as shown in FBC. Further studies are required to better understand HER2 low breast cancer, both generally and in MBC.

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CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
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