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在临床实践中确定HER2阳性乳腺癌亚型是否有益?

Is There a Benefit of HER2-Positive Breast Cancer Subtype Determination in Clinical Practice?

作者信息

Kolářová I, Vaňásek J, Odrážka K, Dušek L, Šinkorová Z, Hlávka A, Štuk J, Stejskal J, Dvořáková D, Sákra L, Mergancová J, Vilasová Z

出版信息

Klin Onkol. 2019 Winter;32(1):25-30. doi: 10.14735/amko2019.

Abstract

BACKGROUND

Breast cancer (BC) with increased expression of human epidermal growth factor receptor 2 with tyrosine kinase activity (HER2+) is a clinically and bio-logically heterogeneous dis-ease. In terms of gene expression, there are four major molecular subtypes - Luminal A, Luminal B, HER2-enriched (HER2-E), and Basal-like. The most common subtype is HER2-E (50- 60%). In hormone-dependent (HR+) HER2-positive tumors, the subgroup HER2-E represents 40- 50% of cases; others are luminal A and B subtypes.

PURPOSE

The aim of this review is to provide information on the significance of the distribution of HER2-positive tumors accord-ing to subtype, which is considered a predictive parameter for guid-ing treatment decisions. For example, HER2-E subtype is characterized by a higher probability of achiev-ing complete pathological remission when treated with chemother-apy and antiHER2 ther-apy, and it is thought that it could be treated us-ing a dual HER2 blockade without chemother-apy. Currently, triple-positive tumors, a specific subtype of breast cancer characterized by HER2+ and HR+, are more often subjects of interest. Their unique bio-logical properties are due to complex interactions between HER2 and estrogen receptor (ER) signalling, which result in lower effectiveness of endocrine ther-apy in these patients than in HR+ and HER2-negative patients and, at the same time, the ER positivity in HER2+ tumors can result in resistance to antiHER2 ther-apy. This type of BC is a non-homogeneous group where the impacts of HER2 positivity on tumor malignant behavior and activity of the estrogen-driven signal-ing pathway are inconsistent. Current studies focus on test-ing new treatments such as dual HER2 block-ing or immunother-apy, in combination with antiHER2 targeted ther-apy with fulvestrant, aromatase inhibitors, cyclin dependent kinase 4/ 6 inhibitors, or inhibitors of the PI3K (phosphatidylinositol-3-kinase) pathway.

CONCLUSION

The distribution of HER2+ BC accord-ing to individual subtype provides information that can contribute to achiev-ing more accurate decisions about the most appropriate ther-apy. Key words breast cancer - subtype - HER2 - trastuzumab - HER2 positive - triple positive - HER2 enriched The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 27. 9. 2018 Accepted: 26. 11. 2018.

摘要

背景

人类表皮生长因子受体2(HER2)表达增加且具有酪氨酸激酶活性的乳腺癌(BC)是一种临床和生物学上异质性的疾病。在基因表达方面,有四种主要分子亚型——腔面A型、腔面B型、HER2富集型(HER2-E)和基底样型。最常见的亚型是HER2-E(50% - 60%)。在激素依赖型(HR+)HER2阳性肿瘤中,HER2-E亚组占病例的40% - 50%;其他为腔面A型和B型亚型。

目的

本综述的目的是提供关于HER2阳性肿瘤按亚型分布的意义的信息,这被认为是指导治疗决策的一个预测参数。例如,HER2-E亚型的特征是在接受化疗和抗HER2治疗时实现完全病理缓解的概率更高,并且有人认为可以在不进行化疗的情况下使用双重HER2阻断进行治疗。目前,三阳性肿瘤,一种以HER2+和HR+为特征的乳腺癌特定亚型,更常成为研究对象。它们独特的生物学特性归因于HER2与雌激素受体(ER)信号之间的复杂相互作用,这导致这些患者内分泌治疗的效果低于HR+和HER2阴性患者,同时,HER2+肿瘤中的ER阳性可导致对抗HER2治疗产生耐药性。这种类型的BC是一个非均质组,其中HER2阳性对肿瘤恶性行为和雌激素驱动信号通路活性的影响不一致。当前研究集中在测试新的治疗方法,如双重HER2阻断或免疫治疗,与抗HER2靶向治疗联合使用氟维司群、芳香化酶抑制剂、细胞周期蛋白依赖性激酶4/6抑制剂或PI3K(磷脂酰肌醇-3-激酶)途径抑制剂。

结论

HER2+ BC按个体亚型的分布提供的信息有助于就最合适的治疗做出更准确的决策。关键词乳腺癌 - 亚型 - HER2 - 曲妥珠单抗 - HER2阳性 - 三阳性 - HER2富集 作者声明他们在研究中使用的药物、产品或服务方面没有潜在的利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的推荐。提交日期:2018年9月27日 接受日期:一2018年11月26日

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