Pathology Unit, Candiolo Cancer Institute FPO-IRCCS, Candiolo, Italy.
Department of Medical Sciences, University of Turin, Turin, Italy.
Pathobiology. 2022;89(5):278-296. doi: 10.1159/000524227. Epub 2022 May 2.
The biomarker human epidermal growth factor receptor-2 (HER2) has represented the best example of successful targeted therapy in breast cancer patients. Based on the concept of "oncogene addiction," we have learnt how to identify patients likely benefitting from anti-HER2 agents. Since HER2 gene amplification leads to marked overexpression of the HER2 receptors on the cell membrane, immunohistochemistry with clinically validated antibodies and scoring system based on intensity and completeness of the membranous expression constitute the screening method to separate negative (score 0/1+) and positive (score 3+) carcinomas and to identify those tumours with complete yet only moderate HER2 expression (score 2+, equivocal carcinomas), which need to be investigated further in terms of gene status to confirm the presence of a loop of oncogene addiction. This process has demanded quality controls and led to recommendations by Scientific Societies, which pathologists routinely need to follow to guarantee reproducibility. In this review, we will span from the description of classical HER2 evaluation to the discussion of those scenarios in which HER2 expression is unusual and/or difficult to define. We will dissect HER2 heterogeneity, HER2 conversion from primary to relapsed/metastatic breast cancer, and we will introduce the new category of HER2-low breast carcinomas.
生物标志物人表皮生长因子受体-2(HER2)是乳腺癌患者成功靶向治疗的最佳范例。基于“癌基因成瘾”的概念,我们已经学会如何识别可能受益于抗 HER2 药物的患者。由于 HER2 基因扩增导致细胞膜上 HER2 受体的过度表达,免疫组织化学结合临床验证的抗体和基于膜表达强度和完整性的评分系统构成了筛选方法,可将阴性(评分 0/1+)和阳性(评分 3+)癌区分开,并识别那些完全但仅中度表达 HER2 的肿瘤(评分 2+,不确定癌),需要进一步调查基因状态以确认致癌基因成瘾环的存在。这一过程需要质量控制,并促使科学协会提出建议,病理学家需要经常遵循这些建议以保证结果的可重复性。在这篇综述中,我们将从经典 HER2 评估的描述扩展到讨论 HER2 表达异常和/或难以定义的情况。我们将剖析 HER2 异质性、原发性至复发/转移性乳腺癌的 HER2 转化,以及引入新的 HER2 低表达乳腺癌类别。