Shang Jiuyan, Sun Xuemei, Xu Zihang, Cai Lijing, Liu Chang, Wu Si, Liu Yueping
Department of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Anesthesia Class, School of Basic Medicine, Hebei Medical University, Shijiazhuang, China.
Front Oncol. 2023 Feb 22;13:1086480. doi: 10.3389/fonc.2023.1086480. eCollection 2023.
The emergence of HER2 antibody-drug conjugates provides new treatment decisions for breast cancer patients, especially those with HER2-low expression. In order to explore the biological characteristics of breast cancer with HER2-low expression, the HER2-low category in primary breast cancer and residual tumor after neoadjuvant therapy was investigated to reflect the evolution of HER2 expression.
HER2 was assessed according to the latest ASCO/CAP guidelines. The cut-off value for staining of HER2-positive cells was >10%. HER2-negative cases were divided into HER2-low (IHC=1+/2+ and no ISH amplification) and HER2-zero (IHC-0), and the clinicopathological characteristics of the cases were collected.
This study included 1140 patients with invasive breast cancer who received preoperative neoadjuvant therapy from 2018 to 2021, of which 365 patients achieved pCR and 775 were non-pCR. In the non-pCR cohort, HER2-low cases accounted for 59.61% of primary tumors and 55.36% of residual tumors. Among HER2-negative cases, HR-positive tumors had a higher incidence of low HER2 expression compared with triple-negative tumors (80.27% vs 60.00% in primary tumors and 72.68% vs 50.77% in residual tumors). The inconsistency rate of HER2 expression was 21.42%, mainly manifested as the conversion of HER2-low cases to HER2-zero (10.19%) and the conversion of HER2-zero to HER2-low (6.45%). Among the HER2-negative cases in the primary tumor, the HER2 discordance rate of HR-positive cases was lower than that of triple-negative cases (23.34% VS 36.92%). This difference was mainly caused by the case switching from HER2-low to HER2-zero. Compared with HER2-zero cases, there were statistically significant differences in RCB grade, MP grade and the number of metastatic lymph nodes in HER2-low cases. Patients with low HER2 expression had a lower pathological response rate and a higher number of metastatic lymph nodes.
HER2-low breast cancer is highly unstable during disease evolution and has certain biological characteristics. HER2-low breast cancer is not only correlated with positive HR, but also has a certain correlation with positive AR. Re-detection of HER2 in breast cancer after neoadjuvant therapy may lead to new treatment opportunities for a certain proportion of patients.
HER2抗体药物偶联物的出现为乳腺癌患者,尤其是HER2低表达患者提供了新的治疗选择。为了探索HER2低表达乳腺癌的生物学特征,对原发性乳腺癌和新辅助治疗后残留肿瘤中的HER2低表达类别进行研究,以反映HER2表达的演变。
根据最新的美国临床肿瘤学会/美国病理学家学会(ASCO/CAP)指南评估HER2。HER2阳性细胞染色的临界值为>10%。HER2阴性病例分为HER2低表达(免疫组化[IHC]=1+/2+且原位杂交[ISH]无扩增)和HER2零表达(IHC-0),并收集病例的临床病理特征。
本研究纳入了2018年至2021年接受术前新辅助治疗的1140例浸润性乳腺癌患者,其中365例达到病理完全缓解(pCR),775例未达到pCR。在未达到pCR的队列中,HER2低表达病例在原发性肿瘤中占59.61%,在残留肿瘤中占55.36%。在HER2阴性病例中,激素受体(HR)阳性肿瘤的HER2低表达发生率高于三阴性肿瘤(原发性肿瘤中分别为80.27%和60.00%,残留肿瘤中分别为72.68%和50.77%)。HER2表达不一致率为21.42%,主要表现为HER2低表达病例转变为HER2零表达(10.19%)以及HER2零表达转变为HER2低表达(6.45%)。在原发性肿瘤的HER2阴性病例中,HR阳性病例的HER2不一致率低于三阴性病例(23.34%对36.92%)。这种差异主要是由HER2低表达病例转变为HER2零表达导致的。与HER2零表达病例相比,HER2低表达病例在残余癌床(RCB)分级、分子病理(MP)分级和转移淋巴结数量方面存在统计学显著差异。HER2低表达患者的病理缓解率较低,转移淋巴结数量较多。
HER2低表达乳腺癌在疾病演变过程中高度不稳定,具有一定的生物学特征。HER2低表达乳腺癌不仅与HR阳性相关,还与雄激素受体(AR)阳性有一定相关性。新辅助治疗后对乳腺癌进行HER2重新检测可能为一定比例的患者带来新的治疗机会。