首页|HER2低表达乳腺癌的临床病理特征及预后分析

HER2低表达乳腺癌的临床病理特征及预后分析

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目的 探讨人表皮生长因子受体2(HER2)低表达乳腺癌的临床病理特征、分子分型及生存预后。方法 收集2016年1月至2021年9月1,684例原发性乳腺癌患者临床资料,其中浸润性导管癌患者1,023例,纳入805例HER2阴性乳腺癌患者,比较HER2低表达和无表达乳腺癌患者在临床病理特征、分子分型及生存预后方面的差异,采用Kaplan-Meier法绘制两组患者DFS和BCSS的生存曲线,Log-rank检验比较生存差异,单因素和多因素Cox比例风险回归模型分析预后影响因素。结果 805例HER2阴性乳腺癌患者中,HER2无表达515例(64。0%),HER2低表达290例(36。0%)。HER2低表达乳腺癌占所有乳腺浸润性导管癌的28。3%,分子分型以Luminal B型为主。与HER2无表达组相比,HER2低表达组中N分期Ⅱ~Ⅲ期(P=0。004)、TNM分期Ⅲ期(P=0。002)、HR阳性患者(P=0。002)的占比更高。805例患者中,HR阳性629例(78。1%),HR阴性176例(21。9%)。629例HR阳性患者中,HER2无表达385例(61。2%),HER2低表达244例(28。8%),HER2低表达较无表达组的确诊年龄小(P=0。031),<45岁(P=0。003)、N分期Ⅱ~Ⅲ期(P=0。001)、TNM分期Ⅲ期(P=0。001)患者的占比更高。176例HR阴性患者中,HER2无表达130例(73。9%),HER2低表达46例(26。1%),与HER2无表达组相比,HER2低表达组患者确诊年龄大(P=0。047),≥45岁占比高(P=0。036),组织学分级(P<0。001)和Ki-67增殖指数(P=0。027)更低。结论 HER2低表达乳腺癌占所有乳腺浸润性导管癌的28。3%,具有独特的临床病理特征和分子分型,HR状态可能是其生物学行为的主要驱动因素。HER2低表达和无表达乳腺癌患者的生存预后均无明显差异。
Objective To investigate the clinicopathological features,molecular typing and prognosis of human epidermal growth factor receptor 2(HER2)low expression breast cancer.Methods We retrospectively collected 1,684 cases of primary invasive breast cancer patients diagnosed and treated in the Breast Disease Center of Zhejiang Provincial Hospital of Chinese Medicine from January 2016 to September 2021,including 1,023 cases of invasive ductal carcinoma,and 805 breast cancer patients with HER2-negative.The differences of clinicopathological features,molecular typing and survival prognosis between HER2-low and HER2-zero breast cancer patients were compared.Kaplan-Meier method was used to plot the survival curves of DFS and BCSS in the two groups.Log-rank test was used to compare the survival differences.Univariate and multivariate Cox proportional hazard regression models were used to analyze the prognostic factors.Results Of the 805 patients with HER2-negative breast cancer,515(64.0%)had HER2 zero expression and 290(36.0%)had HER2 low expression.HER2-low breast cancer accounted for 28.3%of all breast invasive ductal carcinoma,and the molecular typing was mainly Luminal B type.Compared with the HER2-zero group,the proportion of N stage Ⅱ~Ⅲ(P=0.004),TNM stage 3(P=0.002)and HR positive patients(P=0.002)in the HER2-low group was higher.Among the 805 patients,629(78.1%)were HR positive and 176(21.9%)were HR negative.Of the 629 HR-positive patients,385(61.2%)had HER2 zero expression and 244(28.8%)had HER2 low expression.Compared with the HER2-zero group,the HER2-low group had a younger age at diagnosis(P=0.031),a higher proportion of patients<45 years old(P=0.003),N stage Ⅱ~Ⅲ(P=0.001),and TNM stage 3(P=0.001).Among the 176 HR-negative patients,130(73.9%)had HER2 zero expression and 46(26.1%)had HER2 low expression.Compared with the HER2-zero group,the patients in the HER2-low group were older at diagnosis(P=0.047),had a higher proportion of patients≥45 years old(P=0.036),and had lower histological grade(P<0.001)and Ki-67 proliferation index(P=0.027).Conclusion HER2-low breast cancer accounts for 28.3%of all breast invasive ductal carcinoma,with unique clinicopathological features and molecular typing.HR status may be the main driver of the biological behavior of HER2-low breast cancer.There is no significant difference in survival prognosis between HER2-low and HER2-zero breast cancer patients.

Human epidermal growth factor receptor 2Low expressionBreast cancerClinicopathological featuresMolecular typingPrognosis

祝忆婉、黄银、赵煜成、许雷来、谢小红

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310053 浙江中医药大学

310006 浙江省中医院

人表皮生长因子受体2 低表达 乳腺癌 临床病理特征 分子分型 预后

浙江省中医药科技计划

2023ZL416

2024

浙江临床医学
浙江中医药大学 浙江省科普作家协会医学卫生委员会

浙江临床医学

影响因子:0.52
ISSN:1008-7664
年,卷(期):2024.26(4)
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