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  • In Real Life, Low-Level HER...
    Li, Yiqun; Abudureheiyimu, Nilupai; Mo, Hongnan; Guan, Xiuwen; Lin, Shaoyan; Wang, Zijing; Chen, Yimeng; Chen, Shanshan; Li, Qiao; Cai, Ruigang; Wang, Jiayu; Luo, Yang; Fan, Ying; Yuan, Peng; Zhang, Pin; Li, Qing; Ma, Fei; Xu, Binghe

    Frontiers in oncology, 01/2022, Volume: 11
    Journal Article

    To characterize the clinical and pathological features and survival of patients with human epidermal growth factor receptor 2 (HER2)-low breast cancer in China. The China National Cancer Center database was used to identify 1,433 metastatic breast cancer patients with HER2-negative disease diagnosed between 2005 and 2015. Clinicopathological features, survival, and prognosis information were extracted. Overall survival (OS) was estimated using the Kaplan-Meier method and compared using the log-rank test. Prognostic factors associated with OS were analyzed using Cox regression model with 95% confidence interval (95% CI). There were 618 (43.1%) and 815 (56.9%) HER2-low and HER2-zero tumors out of 1,433 tumors, respectively. The proportion of hormone receptor (HR)-positive tumors was significantly higher in HER2-low tumors than in those with HER2-zero tumors (77.8% vs. 69.2%, < 0.001). Patients with HER2-low tumors survived significantly longer than those with HER2-zero tumors in the overall population (48.5 months vs. 43.0 months, = 0.004) and HR-positive subgroup (54.9 months vs. 48.1 months, = 0.011), but not in the HR-negative subgroup (29.5 months vs. 29.9 months, = 0.718). Multivariate regression analysis revealed that HER2-low tumors were independently associated with increased OS in HER2-negative population (HR: 0.85, 95% CI: 0.73-0.98, = 0.026). Our findings demonstrate that HER2-low tumors could be identified as a more distinct clinical entity from HER2-zero tumors, especially for the HR-positive subgroup. A more complex molecular landscape of HER2-low breast cancer might exist, and more precise diagnostic algorithms for HER2 testing could be investigated, thus offering new therapeutic targets for breast cancer treatment.