Kain Zeynep E, Baez-Navarro Ximena, 't Hart Nils A, van Deurzen Carolien H M
Department of Pathology, Erasmus MC, Rotterdam, The Netherlands.
Department of Pathology, Isala Klinieken, Zwolle, The Netherlands.
Virchows Arch. 2025 Sep 16. doi: 10.1007/s00428-025-04266-4.
Patients with HER2-low breast cancer (BC) may be eligible for trastuzumab-deruxtecan (T-DXd) treatment. However, studies have shown that different HER2 antibodies vary in their sensitivity for low HER2 expression, potentially impacting HER2-low BC diagnosis and patient selection for T-DXd. We investigated the frequency of HER2-low BC in relation to the HER2-antibody used across Dutch pathology laboratories. Patients with primary BC without neoadjuvant treatment, diagnosed between 2013 and 2024, were included. HER2-low frequencies from 34 laboratories were obtained from the Dutch Nationwide Pathology Databank (Palga). Additional information (e.g., type of HER2 antibody, staining protocol) was obtained through a questionnaire. A total of 88,713 patients were included, representing 103,505 tumors, of which 94,934 had a conclusive HER2 status. Among non-amplified cases, HER2-low frequencies varied widely across laboratories (33.4%-94.5%), with a gradual increase since 2022. The most commonly used antibody clones were 4B5 (n = 21), DG44 (n = 7), A0485 (n = 4), and SP3 (n = 2). HER2-low proportions were highest with A0485 (71.5%), followed by DG44 (66.7%), SP3 (60.1%), and 4B5 (59.1% with Ultraview, 57.0% with Optiview). Substantial inter-laboratory variation was observed even within the same antibody group (4B5/Ultraview: 40.5%-80.4%; 4B5/Optiview: 37.3%-68.4%; DG44: 40.6%-95.4%; A0485: 62.3%-94.7%; SP3: 31.6%-78.6%). Our data showed a notable variation in HER2-low BC frequency across Dutch pathology laboratories, even among those using the same antibody and detection system. These differences may influence patient eligibility for T-DXd.
HER2低表达乳腺癌(BC)患者可能符合曲妥珠单抗-德曲妥珠单抗(T-DXd)治疗条件。然而,研究表明,不同的HER2抗体对低HER2表达的敏感性各不相同,这可能会影响HER2低表达BC的诊断以及T-DXd治疗的患者选择。我们调查了荷兰各病理实验室中与所使用的HER2抗体相关的HER2低表达BC的发生率。纳入了2013年至2024年期间诊断的未经新辅助治疗的原发性BC患者。从荷兰全国病理数据库(Palga)获取了34个实验室的HER2低表达发生率。通过问卷调查获得了其他信息(例如,HER2抗体类型、染色方案)。总共纳入了88713例患者,代表103505个肿瘤,其中94934个具有明确的HER2状态。在非扩增病例中,各实验室的HER2低表达发生率差异很大(33.4%-94.5%),自2022年以来呈逐渐上升趋势。最常用的抗体克隆为4B5(n = 21)、DG44(n = 7)、A0485(n = 4)和SP3(n = 2)。使用A0485时HER2低表达比例最高(71.5%),其次是DG44(66.7%)、SP3(60.1%)和4B5(使用Ultraview时为59.1%;使用Optiview时为57.0%)。即使在同一抗体组内也观察到了显著的实验室间差异(4B5/Ultraview:40.5%-80.4%;4B5/Optiview:37.3%-68.4%;DG44:40.6%-95.4%;A0485:62.3%-94.7%;SP3:31.6%-78.6%)。我们的数据显示,荷兰各病理实验室中HER2低表达BC的发生率存在显著差异,即使在使用相同抗体和检测系统的实验室之间也是如此。这些差异可能会影响患者接受T-DXd治疗的资格。