Rüschoff Josef, Penner Alexander, Ellis Ian O, Hammond M Elizabeth Hale, Lebeau Annette, Osamura Robert Y, Penault-Llorca Fréderique, Rojo Federico, Desai Chirag, Moh Akira, Atkey Neil, Baenfer Gudrun, Scheel Andreas H, D'Arrigo Corrado, Schildhaus Hans-Ulrich, Viale Giuseppe
From the Discovery Life Sciences Biomarker Services GmbH, Kassel, Germany (Rüschoff, Penner, Baenfer, Schildhaus).
Translational Medical Sciences, School of Medicine, The University of Nottingham, Department of Histopathology, City Hospital Campus, Nottingham University Hospitals, Nottingham, United Kingdom (Ellis).
Arch Pathol Lab Med. 2025 May 1;149(5):431-438. doi: 10.5858/arpa.2024-0052-OA.
CONTEXT.—: Recently, a new type of antibody-drug conjugate, trastuzumab-deruxtecan (T-DXd), has been approved for the treatment of metastatic breast cancer with low level of human epidermal growth factor receptor 2 (HER2) gene expression. Thereby, eligibility relies on an accurate diagnosis of HER2-low status defined by immunohistochemistry IHC 1+/2+ with no gene amplification.
OBJECTIVE.—: To assess pathologists' accuracy and training efficacy in the diagnosis of HER2-low.
DESIGN.—: Agreement rates of HER2-low scoring in breast cancer tissue were assessed between expert consensus and real-world pathologists (n = 77 from 14 countries) before and after a specific 4-hour training program for HER2-low detection. Two assays were evaluated, the Ventana Pathway 4B5 CDx and the Dako HercepTest (polyclonal). Concordance of the pathologists with consensus score and efficacy of training were measured by Cohen κ, overall rater agreement, and receiver operating characteristic (ROC) curve statistics.
RESULTS.—: In the Ventana 4B5 HER2-low category, baseline agreement rates were >80% but <90%. Negative percentage agreement was improved from 80.6% to 91.1% by training. In the HER2-0 category, positive percentage agreement (74.6%) was the only parameter below the 80% benchmark but was significantly improved to 89.2% after training. Training efficacy was confirmed by ROC curve analysis, which shows improvement for the identification of HER2-0 and HER2-low cases. Finally, in-depth examination of cases with discordant HER2 status disclosed specific issues of HER2-low underscoring and overscoring.
CONCLUSIONS.—: The ability of pathologists to achieve acceptable diagnostic accuracy in identifying patients with HER2-low breast cancer could be enhanced by short-term training. Potential routes to improve the quality of HER2-low scoring in clinical practice have been identified.
最近,一种新型抗体药物偶联物曲妥珠单抗-德曲妥珠单抗(T-DXd)已被批准用于治疗人表皮生长因子受体2(HER2)基因表达水平低的转移性乳腺癌。因此, eligibility依赖于通过免疫组织化学(IHC)1+/2+且无基因扩增来准确诊断HER2低状态。
评估病理学家在诊断HER2低状态时的准确性和培训效果。
在针对HER2低检测的特定4小时培训项目前后,评估专家共识与来自14个国家的77名实际病理学家对乳腺癌组织中HER2低评分的一致率。评估了两种检测方法,即Ventana Pathway 4B5 CDx和Dako HercepTest(多克隆)。通过Cohen κ、总体评分者一致性和受试者操作特征(ROC)曲线统计来衡量病理学家与共识评分的一致性以及培训效果。
在Ventana 4B5 HER2低类别中,基线一致率>80%但<90%。通过培训,阴性百分比一致性从80.6%提高到了91.1%。在HER2-0类别中,阳性百分比一致性(74.6%)是唯一低于80%基准的参数,但培训后显著提高到了89.2%。ROC曲线分析证实了培训效果,显示在识别HER2-0和HER2低病例方面有所改善。最后,对HER2状态不一致的病例进行深入检查,发现了HER2低评分不足和过度评分的具体问题。
通过短期培训可以提高病理学家在识别HER2低乳腺癌患者时达到可接受诊断准确性的能力。已确定了在临床实践中提高HER2低评分质量的潜在途径。