International Expert Consensus Recommendations for HER2 Reporting in Breast Cancer: Focus on HER2-Low and Ultralow Categories

IF 6.6 1区 医学 Q1 PATHOLOGY
Modern Pathology Pub Date : 2026-01-01 Epub Date: 2025-10-28 DOI:10.1016/j.modpat.2025.100925
Emad A. Rakha , Puay Hoon Tan , Mieke R. Van Bockstal , Kimberly H. Allison , Edi Brogi , Grace Callagy , Gábor Cserni , Shabnam Jaffer , Maria Pia Foschini , Helenice Gobbi , Janina Kulka , Xiaoxian Li , Elena Provenzano , Abeer M. Shaaban , Gary M. Tse , Zsuzsanna Varga , Anne Vincent-Salomon , Rin Yamaguchi , Wentao Yang , Soha ElSheikh , Cecily Quinn
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引用次数: 0

Abstract

The concept of “HER2-negative” breast cancer is evolving, with the recognition of HER2-low and HER2-ultralow subsets. These subsets are clinically relevant regarding treatment with the antibody-drug conjugate trastuzumab deruxtecan (T-DXd), which has shown survival benefit in patients with metastatic carcinoma with minimal HER2 protein expression that lack HER2 gene amplification by in situ hybridization. In clinical trials using T-DXd, HER2-low was defined as an immunohistochemistry (IHC) score 1+ or an IHC score 2+ without HER2 gene amplification. HER2-ultralow was defined as faint or barely perceptible, incomplete membrane staining in >0% to ≤10% of tumor cells (IHC score 0+/with membrane staining) and HER2-null as the complete absence of staining (IHC score 0/absent membrane staining). These results now necessitate more detailed evaluation and reporting of traditional “HER2-negative” results to identify patients with metastatic breast cancer who may benefit from T-DXd therapy. Both the US Food and Drug Administration and the European Medicines Agency have extended the regulatory approval of T-DXd to patients with metastatic breast cancer showing HER2-low or HER2-ultralow expressions. Updated clinical management guidelines now, therefore, incorporate the spectrum of HER2 results into treatment selection algorithms in the metastatic setting. To align histopathologic practice with these developments, the College of American Pathologists has issued a new biomarker-reporting template that recommends explicit distinction between IHC 0/absent membrane staining and IHC 0+/with membrane staining. Key concerns among pathologists include assay variability, scoring reproducibility, and quality assurance standards for accurately detecting such low levels of HER2 expression. This manuscript provides expert consensus, evidence-based practical recommendations for identifying and reporting tumors with HER2-low and HER2-ultralow expression. We emphasize standardized testing protocols, validated assays, robust internal and external controls, and focused training for pathologists. A universal structured pathology report is proposed to highlight the accurate distinction between IHC 0 (null), IHC 0+ (ultralow), and HER2-low expressions.
乳腺癌HER2报告的国际专家共识建议:关注HER2低和超低类别。
随着her2低亚群和her2超低亚群的认识,“her2阴性”乳腺癌的概念也在不断发展。这些亚群与抗体-药物偶联曲妥珠单抗德鲁西替康(T-DXd)的治疗具有临床相关性,该药物已显示出HER2蛋白表达极低且缺乏HER2基因原位杂交(ISH)扩增的转移性癌患者的生存益处。在使用T-DXd的临床试验中,HER2-low被定义为免疫组织化学(IHC)评分1+或IHC评分2+,没有HER2基因扩增。her2 -超低定义为肿瘤细胞中有0 ~ 10%的肿瘤细胞出现微弱或几乎无法察觉的不完全膜染色(IHC评分0+/伴有膜染色),her2 -零定义为完全无染色(IHC评分0/伴有膜染色)。这些结果现在需要对传统的“her2阴性”结果进行更详细的评估和报告,以确定可能从T-DXd治疗中受益的转移性乳腺癌患者。美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)已将T-DXd的监管批准延长至her2低或her2超低表达的转移性乳腺癌患者。因此,现在更新的临床管理指南将HER2结果谱纳入转移性肿瘤的治疗选择算法中。为了使组织病理学实践与这些发展保持一致,美国病理学家学会(CAP)发布了一个新的生物标志物报告模板,建议明确区分IHC 0/无膜染色和IHC 0+/有膜染色。病理学家主要关注的问题包括测定的可变性、评分的可重复性和准确检测如此低水平HER2表达的质量保证标准。该手稿提供了专家共识,基于证据的实用建议,用于识别和报告her2低和her2超低表达的肿瘤。我们强调标准化的检测方案,有效的分析,强大的内部和外部控制,以及对病理学家的重点培训。提出一份通用的结构化病理报告,以强调IHC 0(零)、IHC 0+(超低)和her2低表达之间的准确区分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Modern Pathology
Modern Pathology 医学-病理学
CiteScore
14.30
自引率
2.70%
发文量
174
审稿时长
18 days
期刊介绍: Modern Pathology, an international journal under the ownership of The United States & Canadian Academy of Pathology (USCAP), serves as an authoritative platform for publishing top-tier clinical and translational research studies in pathology. Original manuscripts are the primary focus of Modern Pathology, complemented by impactful editorials, reviews, and practice guidelines covering all facets of precision diagnostics in human pathology. The journal's scope includes advancements in molecular diagnostics and genomic classifications of diseases, breakthroughs in immune-oncology, computational science, applied bioinformatics, and digital pathology.
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