Sode Michael, Thagaard Jeppe, Eriksen Jens Ole, Laenkholm Anne-Vibeke
Department of Pathology, Zealand University Hospital, Roskilde, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Histopathology. 2023 May;82(6):912-924. doi: 10.1111/his.14877. Epub 2023 Mar 1.
Digital image analysis (DIA) is used increasingly as an assisting tool to evaluate biomarkers, including human epidermal growth factor receptor 2 (HER2) in invasive breast cancer (BC). DIA can assist pathologists in HER2 evaluation by presenting quantitative information about the HER2 staining in APP assisted reading (AR). Concurrently, the HER2-low category (HER2-1+/2+ without HER2 gene amplification) has gained prominence due to newly developed antibody-drug conjugates. However, major inter- and intraobserver variability have been observed for the entity. The present quality assurance study investigated the concordance between DIA and AR in clinical use, especially concerning the HER2-low category.
HER2 immunohistochemistry (IHC) in 761 tumours from 727 patients was evaluated in tissue microarray (TMA) cores by DIA (Visiopharm HER2-CONNECT) and AR. Overall concordance between HER2-scores were 73% (n = 552, weighted-κ: 0.66), and 88% (n = 669, weighted-κ: 0.70), when combining HER2-0/1+. A total of 205 scores were discordant by one category, while four were discordant by two categories. A heterogeneous HER2 pattern was relatively common in the discordant cases and a pitfall in the categorisation of HER2-low BC. AR more commonly reassigned a lower HER2 score (from HER2-1+ to HER2-0) within the HER2-low subgroup (n = 624) compared with DIA.
DIA and AR display moderate agreement with heterogeneous and aberrant staining, representing a source of discordance and a pitfall in the evaluation of HER2.
数字图像分析(DIA)越来越多地被用作评估生物标志物的辅助工具,包括浸润性乳腺癌(BC)中的人表皮生长因子受体2(HER2)。DIA可通过在应用辅助阅片(AR)中提供有关HER2染色的定量信息,协助病理学家进行HER2评估。同时,由于新开发的抗体药物偶联物,HER2低表达类别(HER2 1+/2+且无HER2基因扩增)受到了更多关注。然而,已观察到该实体在观察者间和观察者内存在较大变异性。本质量保证研究调查了临床应用中DIA和AR之间的一致性,特别是关于HER2低表达类别。
通过DIA(Visiopharm HER2-CONNECT)和AR对727例患者的761个肿瘤组织微阵列(TMA)芯进行HER2免疫组织化学(IHC)评估。当合并HER2-0/1+时,HER2评分的总体一致性为73%(n = 552,加权κ值:0.66),以及88%(n = 669,加权κ值:0.70)。共有205个评分在一个类别上不一致,而有4个在两个类别上不一致。在不一致的病例中,HER2异质性模式相对常见,这是HER2低表达BC分类中的一个陷阱。与DIA相比,AR在HER2低表达亚组(n = 624)中更常将较低的HER2评分重新分类(从HER2 1+降至HER2-0)。
DIA和AR在异质性和异常染色方面显示出中等程度的一致性,这是HER2评估中不一致的一个来源和陷阱。