Department of Breast Surgery, National Cancer Center|National Clinical Research Center for Cancer|Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
State Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, National Cancer Center| National Clinical Research Center for Cancer| Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Target Oncol. 2024 Jan;19(1):81-93. doi: 10.1007/s11523-023-01030-z. Epub 2024 Jan 24.
The prognostic impact of HER2-low on overall survival (OS) and disease-free survival (DFS) in patients with resectable breast cancer (BC) remains controversial, partly resulting from the hormone receptor (HR) status.
To investigate the prognostic impact of HER2-low in different HR subgroups.
We retrospectively retrieved medical records of treatment-naive primary HER2-low and HER2-zero BC patients who were diagnosed with invasive ductal carcinoma and underwent surgery in the Cancer Hospital of the Chinese Academy of Medical Sciences from January 2009 to September 2017 (n = 7371). We compared the clinicopathologic features and performed Cox regression and landmark survival analyses to explore the prognostic impact of HER2-low on survival outcomes during distinct post-surgery intervals-36 months, 60 months, and 120 months.
HER2-low BC, compared to HER2-zero BC, exhibited less aggressive clinicopathologic features, such as smaller invasion size, lower grade, increased nerve invasion, higher HR positivity, and a higher proportion of low-Ki67 cases. In the HR-positive subgroup, HER2-low demonstrated improved OS (p = 0.046) and DFS (p = 0.026) within 60 months. Conversely, HER2-low displayed worse DFS (p = 0.046) in the HR-negative subgroup after 36 months from surgery. The findings remained robust in uni- and multi-variable Cox models.
HER2-low BCs manifested less aggressive clinicopathologic features than the HER2-zero cases. The prognostic impact of HER2-low in resectable BCs exhibits variability contingent upon the patients' HR status.
HER2 低表达对可切除乳腺癌(BC)患者总生存(OS)和无病生存(DFS)的预后影响仍存在争议,部分原因是激素受体(HR)状态。
探讨 HER2 低表达在不同 HR 亚组中的预后影响。
我们回顾性检索了 2009 年 1 月至 2017 年 9 月在中国医学科学院肿瘤医院接受手术治疗的初治原发性 HER2 低表达和 HER2 零表达浸润性导管癌 BC 患者的病历资料(n=7371)。我们比较了临床病理特征,并进行 Cox 回归和里程碑生存分析,以探讨 HER2 低表达在不同手术后时间间隔(36 个月、60 个月和 120 个月)对生存结果的预后影响。
与 HER2 零表达 BC 相比,HER2 低表达 BC 表现出侵袭性较小的临床病理特征,如肿瘤体积较小、组织学分级较低、神经浸润增加、HR 阳性率较高以及 Ki67 低表达比例较高。在 HR 阳性亚组中,HER2 低表达在 60 个月内显示出更好的 OS(p=0.046)和 DFS(p=0.026)。相反,在 HR 阴性亚组中,HER2 低表达在手术后 36 个月后显示出更差的 DFS(p=0.046)。这些发现在单变量和多变量 Cox 模型中仍然稳健。
HER2 低表达 BC 比 HER2 零表达病例表现出侵袭性较小的临床病理特征。HER2 低表达在可切除 BC 中的预后影响因患者 HR 状态而异。