Núñez Álvarez Violeta, González Castilla Belén, Fernández Rivero Belén, Hernández Carrasco María, Lluch Gómez Jaime, Sánchez Lobón Irene, Ocaña de la Rosa María Ángeles, Menguiano Romero Yulema, Perdomo Zaldívar Eduardo, Rodríguez Pérez Lourdes, Benítez Rodríguez Encarnación, Baena Cañada José Manuel
Servicio de Oncología Médica (Medical Oncology Department), Hospital Universitario Puerta del Mar, Avenida de Ana de Viya 21, 11009, Cádiz, Spain.
Instituto de Investigación E Innovación Biomédica de Cádiz (Cadiz Institute for Biomedical Research and Innovation), Cadiz, Spain.
Clin Transl Oncol. 2025 Sep 3. doi: 10.1007/s12094-025-04053-2.
Human epidermal growth factor receptor 2 (HER2)-negative breast cancer includes HER2-zero and HER2-low tumors. Whether their clinical features and survival are different is not fully clarified. The objective was to explore their clinicopathologic differences and survival.
METHODS/PATIENTS: Retrospective analysis of HER2-negative, stage I-III breast cancer patients from 2006 to 2016 at a single site. Clinicopathological variables, events and survival are analyzed, comparing HER2-low and HER2-zero cases.
Of 535 patients, 351 (65.61%) were HER2-zero and 184 (34.39%) HER2-low (154 (83.70%) score 1 + and 30 (16.30%) score 2 +). The proportion of premenopausal women was higher in the HER2-low subgroup (50.50% vs 39.40%, p = 0.016). For those with HER2-zero tumors, 15.70% were estrogen receptor (ER) negative, whereas only 9.20% (p = 0.045) of HER2-low tumors were ER negative. In HER2-low/ER negative tumors, tumor size, histologic grade, and Ki67 levels were higher. Patients with HER2-zero/ER-negative tumors were younger, had fewer comorbidities, less nodal involvement, a higher frequency of ductal histopathology, and, again, higher histologic grade and Ki67 levels. There were no differences in the events. The overall survival probability at 11.50 years in the HER2-zero subgroup was 0.51 (95% confidence interval (CI 95%) 0.28-0.74) and in the HER2-low subgroup 0.67 (95% CI 0.56-0.77) (p = 0.52).
HER2-zero and HER2-low breast cancers are not distinct clinicopathologic entities. The differences detected in some variables seem to depend on ER status. No prognostic differences were observed.
人表皮生长因子受体2(HER2)阴性乳腺癌包括HER2零表达和HER2低表达肿瘤。它们的临床特征和生存率是否不同尚未完全明确。目的是探讨它们的临床病理差异和生存率。
方法/患者:对2006年至2016年在单一机构的HER2阴性、Ⅰ - Ⅲ期乳腺癌患者进行回顾性分析。分析临床病理变量、事件和生存率,比较HER2低表达和HER2零表达病例。
535例患者中,351例(65.61%)为HER2零表达,184例(34.39%)为HER2低表达(154例(83.70%)评分为1 +,30例(16.30%)评分为2 +)。HER2低表达亚组中绝经前女性的比例更高(50.50%对39.40%,p = 0.016)。HER2零表达肿瘤患者中,15.70%为雌激素受体(ER)阴性,而HER2低表达肿瘤中只有9.20%(p = 0.045)为ER阴性。在HER2低表达/ER阴性肿瘤中,肿瘤大小、组织学分级和Ki67水平更高。HER2零表达/ER阴性肿瘤患者更年轻,合并症更少,淋巴结受累更少,导管组织病理学频率更高,并且组织学分级和Ki67水平再次更高。事件方面无差异。HER2零表达亚组11.50年时的总生存概率为0.51(95%置信区间(CI 95%)0.28 - 0.74),HER2低表达亚组为0.67(95% CI 0.56 - 0.77)(p = 0.52)。
HER2零表达和HER2低表达乳腺癌并非不同的临床病理实体。在一些变量中检测到的差异似乎取决于ER状态。未观察到预后差异。