Sun Teng, Wang Tong, Li Xiangjun, Wang Haibo, Mao Yan
Department of Surgery, School of Clinical Medicine, Qingdao University, Qingdao, China.
Breast Disease Center, The Affiliated Hospital of Qingdao University, Qingdao, China.
Front Oncol. 2023 Jun 20;13:1148228. doi: 10.3389/fonc.2023.1148228. eCollection 2023.
It has been reported that breast cancer (BC) with low expression of human epidermal growth factor receptor 2 (HER2) might be a distinct subtype of BC. However, the prognostic effect of low HER2 expression on BC patients remains controversial. We aim to conduct this single-institution retrospective analysis to assess HER2-low-positive BC outcomes in Chinese women and the prognostic role of TILs in HER2-low-positive early-stage BC.
We retrospectively enrolled 1,763 BC patients treated in a single institution from 2017 to 2018. TILs are regarded as continuous variables and are divided into low TILs (≤10%) and high TILs (>10%) for statistical analysis. Univariate and multivariable Cox proportional hazards regression models were used to test the associations between TILs and disease-free survival (DFS) with adjustment for clinicopathologic characteristics.
High TIL levels (>10%) were associated with tumor size (>2 cm, p = 0.042), age at diagnosis (p = 0.005), Ki-67 index (>25%; p <0.001), HR (hormone receptor) status (positive, p <0.001), advanced pathological stage (p = 0.043), subtype (p <0.001), and HER2 status (p <0.001). The Kaplan-Meier analysis indicated that no significant difference in DFS (p = 0.83) could be found between HER2-positive, HER2-low-positive, and HER2-0 BC. The DFS of HER2-low-positive BC and HER2-nonamplified BC with high levels of TILs was statistically better than that of patients with low levels of TILs (p = 0.015; p = 0.047). In HER2-low-positive BC patients with high TIL levels (>10%), DFS was significantly improved in both the univariate (HR = 0.44, 95% CI 0.22-0.87, P = 0.018) and multivariate (HR = 0.47, 95% CI 0.23-0.95, P = 0.035) Cox models. For further subgroup analysis, HR (+)/HER2-low-positive BC with high TIL (>10%) levels was associated with improved DFS in both the univariate (HR = 0.41, 95% CI 0.19-0.90, P = 0.025) and multivariate (HR = 0.42, 95% CI 0.19-0.93, P = 0.032) Cox models. The HR (-)/HER2-0 BC with high TIL (>10%) level was not statistically significant in the univariate Cox model, but it was statistically significant in the multivariate (HR = 0.16, 95% CI 0.28-0.96, P = 0.045) Cox model.
Among early-stage BC, no significant survival difference could be found between the HER2-positive, HER2-low-positive, and HER2-0 cohorts. High levels of TILs were significantly associated with improved DFS in HER2-low-positive patients, especially in the HR (+)/HER2-low-positive subtype.
据报道,人表皮生长因子受体2(HER2)低表达的乳腺癌(BC)可能是BC的一种独特亚型。然而,HER2低表达对BC患者的预后影响仍存在争议。我们旨在进行这项单机构回顾性分析,以评估中国女性HER2低表达阳性BC的预后以及肿瘤浸润淋巴细胞(TILs)在HER2低表达阳性早期BC中的预后作用。
我们回顾性纳入了2017年至2018年在单一机构接受治疗的1763例BC患者。TILs被视为连续变量,并分为低TILs(≤10%)和高TILs(>10%)进行统计分析。使用单变量和多变量Cox比例风险回归模型来检验TILs与无病生存期(DFS)之间的关联,并对临床病理特征进行校正。
高TIL水平(>10%)与肿瘤大小(>2 cm,p = 0.042)、诊断年龄(p = 0.005)、Ki-67指数(>25%;p <0.001)、激素受体(HR)状态(阳性,p <0.001)、晚期病理分期(p = 0.043)、亚型(p <0.001)和HER2状态(p <0.001)相关。Kaplan-Meier分析表明,HER2阳性、HER2低表达阳性和HER2阴性BC之间的DFS无显著差异(p = 0.83)。HER2低表达阳性BC和TILs水平高的HER2非扩增BC的DFS在统计学上优于TILs水平低的患者(p = 0.从2017年到2018年,我们回顾性地招募了1763名在单一机构接受治疗的乳腺癌患者。肿瘤浸润淋巴细胞被视为连续变量,并分为低肿瘤浸润淋巴细胞(≤10%)和高肿瘤浸润淋巴细胞(>10%)进行统计分析。单变量和多变量Cox比例风险回归模型用于检验肿瘤浸润淋巴细胞与无病生存期之间的关联,并对临床病理特征进行调整。
高肿瘤浸润淋巴细胞水平(>10%)与肿瘤大小(>2厘米,p = 0.042)、诊断年龄(p = 0.005)、Ki-67指数(>25%;p <0.001)、激素受体状态(阳性,p <0.001)、晚期病理分期(p = 0.043)、亚型(p <0.001)和HER2状态(p <0.001)相关。Kaplan-Meier分析表明,HER2阳性、HER2低表达阳性和HER2阴性乳腺癌之间的无病生存期无显著差异(p = 0.83)。HER2低表达阳性乳腺癌和肿瘤浸润淋巴细胞水平高的HER2非扩增乳腺癌的无病生存期在统计学上优于肿瘤浸润淋巴细胞水平低的患者(p = 0.015;p = 0.047)。在肿瘤浸润淋巴细胞水平高(>10%)的HER2低表达阳性乳腺癌患者中,单变量(HR = 0.44,95%置信区间0.22-0.87,P = 0.018)和多变量(HR = 0.47,95%置信区间0.23-0.95,P = 0.035)Cox模型均显示无病生存期显著改善。进一步的亚组分析表明,肿瘤浸润淋巴细胞水平高(>10%)的HR(+)/HER2低表达阳性乳腺癌在单变量(HR = 0.41,95%置信区间0.19-0.90,P = 0.025)和多变量(HR = 0.42,95%置信区间0.19-0.93,P = 0.032)Cox模型中均与无病生存期改善相关。肿瘤浸润淋巴细胞水平高(>10%)的HR(-)/HER2阴性乳腺癌在单变量Cox模型中无统计学意义,但在多变量(HR = 0.16,95%置信区间0.28-0.96,P = 0.045)Cox模型中有统计学意义。
在早期乳腺癌中,HER2阳性、HER2低表达阳性和HER阴性队列之间未发现显著的生存差异。高肿瘤浸润淋巴细胞水平与HER2低表达阳性患者的无病生存期显著改善相关,尤其是在HR(+)/HER2低表达阳性亚型中。 015;p = 0.047)。在TILs水平高(>10%)的HER2低表达阳性BC患者中,单变量(HR = 0.44,95%CI 0.22-0.87,P = 0.018)和多变量(HR = 0.47,95%CI 0.23-0.95,P = 0.035)Cox模型均显示DFS显著改善。对于进一步的亚组分析,TILs水平高(>10%)的HR(+)/HER2低表达阳性BC在单变量(HR = 0.41,95%CI 0.19-0.90,P = 0.025)和多变量(HR = 0.42,95%CI 0.19-0.93,P = 0.032)Cox模型中均与DFS改善相关。TILs水平高(>10%)的HR(-)/HER2-0 BC在单变量Cox模型中无统计学意义,但在多变量(HR = 0.16,95%CI 0.28-0.96,P = 0.045)Cox模型中有统计学意义。
在早期BC中,HER2阳性、HER2低表达阳性和HER2-0队列之间未发现显著的生存差异。高TILs水平与HER2低表达阳性患者的DFS显著改善相关,尤其是在HR(+)/HER2低表达阳性亚型中。