Zeng Yi, Qian Pengfei, Li Guanhong, Sun Yu
Department of Breast Surgery, The Affiliated Huizhou Hospital, Guangzhou Medical University, No.1 Xuebei Road, Huizhou, Guangdong, 516000, China.
World J Surg Oncol. 2025 Sep 5;23(1):331. doi: 10.1186/s12957-025-03962-4.
HER2-negative breast cancers can be further subclassified into HER2-low and HER2-zero subtypes. The DESTINY-Breast04 trial has established HER2-low as a research hotspot, with recent studies indicating superior survival rates in HER2-low patients than HER2-zero patients. The impact of heterogeneous hormone receptor (HR) expression patterns on HER2-negative breast cancer has not been comprehensively investigated. This study explored how varying ER and PR expression patterns affect survival rates in patients with HER2-negative breast cancer.
This retrospective study comprised 648 HER2-negative breast cancer patients treated at our hospital between 2010 and 2023. Six subgroups were compared, including ER+/PR+/HER2-low, ER+/PR+/HER2-zero, single HR+/HER2-low, single HR/HER2-zero, ER-/PR-/HER2-low, and ER-/PR-/HER2-zero.
With disease-free survival and overall survival as primary endpoints, the cohort included 648 HER2-negative breast cancer patients. Compared to HER2-zero, HER2-low patients showed a higher proportion of ER positivity (q = 0.016). The ER+/PR + group exhibited a higher proportion of HER2-low, lower N stage, lower histological grade, and lower Ki-67% (p < 0.001), and were also more likely to achieve pCR after neoadjuvant therapy. In the overall population, HER2-low exhibited better survival outcomes. Compared to single HR+/HER2-low, ER+/PR+/HER2-low had longer DFS (p < 0.001). HER2-low is an independent prognostic factor for survival outcomes in HER2-negative patients.
Our findings suggest that HER2-low breast cancer is associated with improved survival outcomes compared to HER2-zero breast cancer. HER2-low breast cancer exhibits different survival outcomes across different HR subgroups. These findings may guide future biomarker-driven treatment strategies in HER2-negative breast cancer.
人表皮生长因子受体2(HER2)阴性乳腺癌可进一步细分为HER2低表达和HER2零表达亚型。DESTINY-Breast04试验已将HER2低表达确立为一个研究热点,最近的研究表明HER2低表达患者的生存率高于HER2零表达患者。异质性激素受体(HR)表达模式对HER2阴性乳腺癌的影响尚未得到全面研究。本研究探讨了雌激素受体(ER)和孕激素受体(PR)表达模式的变化如何影响HER2阴性乳腺癌患者的生存率。
本回顾性研究纳入了2010年至2023年期间在我院接受治疗的648例HER2阴性乳腺癌患者。比较了六个亚组,包括ER+/PR+/HER2低表达、ER+/PR+/HER2零表达、单一HR+/HER2低表达、单一HR/HER2零表达、ER-/PR-/HER2低表达和ER-/PR-/HER2零表达。
以无病生存期和总生存期为主要终点,该队列包括648例HER2阴性乳腺癌患者。与HER2零表达相比,HER2低表达患者的ER阳性比例更高(q = 0.016)。ER+/PR+组的HER2低表达比例更高、N分期更低、组织学分级更低、Ki-67%更低(p < 0.001),并且在新辅助治疗后更有可能实现病理完全缓解(pCR)。在总体人群中,HER2低表达表现出更好的生存结果。与单一HR+/HER2低表达相比,ER+/PR+/HER2低表达的无病生存期更长(p < 0.001)。HER2低表达是HER2阴性患者生存结果的独立预后因素。
我们的研究结果表明,与HER2零表达乳腺癌相比,HER2低表达乳腺癌与更好的生存结果相关。HER2低表达乳腺癌在不同的HR亚组中表现出不同的生存结果。这些发现可能会指导未来HER2阴性乳腺癌中基于生物标志物的治疗策略。