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Impact of hormone receptor, HER2, and Ki-67 status conversions on survival after neoadjuvant chemotherapy in breast cancer patients: a retrospective study

Authors :
Yuhai, Chen
Xiaoyan, Liu
Keda, Yu
Xiangyu, Sun
Shouping, Xu
Pengfei, Qiu
Zhidong, Lv
Xinwen, Zhang
Ayao, Guo
Yingying, Xu
Source :
Ann Transl Med
Publication Year :
2022
Publisher :
AME Publishing Company, 2022.

Abstract

BACKGROUND: The discordance of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and Ki-67 cell nuclear proliferation antigen status in patients with locally advanced breast cancer pre- and post-neoadjuvant chemotherapy (NAC) is quite common. This study aimed to assess the frequency of changes in receptor status after NAC in patients with invasive ductal breast cancer and the prognostic impact of such changes. METHODS: The study comprised 670 patients who were diagnosed with invasive ductal breast carcinoma and treated with both NAC and surgery from 2012–2017. Hormone receptor (HR; including ER and PR), HER2, and Ki-67 status was assessed before NAC and in residual invasive tumor cells of the surgical specimens. The prognostic impact of receptor conversions in breast cancer patients treated with NAC was evaluated in this retrospective study. RESULTS: The conversion of ER was related to overall survival (OS; P=0.008) and disease-free survival (DFS; P=0.004). Patients whose ER status was always positive had the best prognosis, and those who were always negative had the worst prognosis. Similar results were also found for PR status, as the conversion of PR status was also related to OS (P20% after NAC had the worst survival. Nevertheless, there was no statistical significance in the conversion of HER2 status. In multivariate Cox regression analyses, PR conversion and post-neoadjuvant pathological lymph node stage (ypN) were independent prognostic factors for DFS (P=0.008

Details

ISSN :
23055847 and 23055839
Volume :
10
Database :
OpenAIRE
Journal :
Annals of Translational Medicine
Accession number :
edsair.doi.dedup.....8be9ba8e27b0df988a7e4d034dac4bd8