Pathological complete response rate and clinical outcome after neoadjuvant therapy of HER2-low breast cancer: A National Cancer Database Analysis

被引:4
作者
Zhong, Guansheng [1 ]
Song, Dajiang [2 ]
Lou, Weiyang [1 ]
Wei, Bajin [1 ]
Chen, Yaomin [1 ]
Cui, Haidong [1 ]
Hu, Jingjing [3 ]
Dong, Huaying [4 ]
Chen, Jie [5 ]
Dai, Zhijun [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Breast Surg, Hangzhou, Peoples R China
[2] Hunan Prov Canc Hosp, Dept Oncol Plast Surg, Changsha, Peoples R China
[3] Massachusetts Gen Canc Ctr, 55 Fruit St, Boston, MA 02114 USA
[4] Hainan Med Univ, Hainan Gen Hosp, Hainan Affiliated Hosp, Dept Gen Surg, Haikou, Peoples R China
[5] Jinyun Peoples Hosp, Dept Gen Surg, Lishui, Peoples R China
来源
EJSO | 2023年 / 49卷 / 11期
基金
中国国家自然科学基金;
关键词
Breast cancer; HER2; low; Complete respond rate; NCDB; Survival;
D O I
10.1016/j.ejso.2023.06.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The interest in breast cancer with low HER2 expression as a distinct subtype is increasing. We aimed to explore the differences between HER2-low and HER2-zero breast cancer in their prognosis and rate of pathological complete response (pCR) after neoadjuvant therapy. Methods: The National Cancer Database (NCDB) was used to select patients with breast cancer who received neoadjuvant therapy from 2004 to 2017. Logistic regression model was constructed for analysis of pCR. Cox proportional hazards regression model and Kaplan-Meier method were used for survival analysis.Results: A total of 41500 breast cancer patients were included, among which 14814 (35.7%) had HER2zero tumors and 26686 (64.3%) had HER2-low. HER2-low tumors were more commonly HR-positive in comparison with HER2-zero (66.3% versus 47.1%, P < 0.001). A lower rate of pCR was observed in HER2-low tumors than in HER2-zero tumors after neoadjuvant therapy in the total cohort (OR = 0.90; 95% CI [0.86-0.95]; P < 0.001) and in the subset of HR-positive (OR = 0.87; 95% CI [0.81-0.94]; P < 0.001). Patients with HER2-low tumors had a significantly superior survival than those with HER2zero tumors (HR = 0.90; 95% CI [0.86-0.94]; P < 0.001), regardless of the HR status. Additionally, a marginal survival difference was also observed between HER2 IHC1+ and HER2 IHC2+/ISH-negative (HR = 0.91; 95% CI [0.85-0.97]; P = 0.003) cohorts.Conclusion: HER2-low tumors are a clinically relevant breast cancer subtype that is distinct from HER2zero tumors. These findings may provide clues to appropriate therapeutic strategies for this subtype in the future. (c) 2023 Published by Elsevier Ltd.
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页数:7
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