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Updated: Jan 16, 2026
Building Up a High-throughput Screening Platform to Assess the Heterogeneity of HER2 Gene Amplification in Breast Cancers
Published on: December 5, 2017
Influence of HER2-low and HER2-zero status on pathologic complete response and survival in triple-negative breast
Yu Qin1, Chenchen Pu1, Yuping Fan1
1The Affiliated Nanchong Central Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.
Objective:
To delve into the influence of different status of human epidermal growth factor receptor 2 (HER2) on the long-term survival of patients suffering from triple-negative breast cancer (TNBC), as well as the pathological complete response (pCR) following neoadjuvant therapy (NAT) via meta-analysis.
Methods:
A computer search in the Embase, PubMed, Web of Science, and Cochrane Library databases was executed up to January 13, 2025, to collect studies related to HER2 status in TNBC patients. The articles were screened per the inclusion and exclusion criteria. The required data were extracted. The study quality was appraised by means of the Newcastle-Ottawa Scale, and statistical analysis was carried out utilizing Stata 15.0 software.
Results:
36 studies involving 54,277 patients with TNBC were included. According to the meta-analysis, the pCR rate after NAT was more notable in the HER2-zero group compared to the HER2-low group (RR = 0.90, 95%CI: 0.86-0.93, P < 0.001). Regarding overall survival (OS), HER2-low patients exhibited a better prognosis (HR = 0.93, 95%CI: 0.90-0.97, P < 0.001). For disease-free survival, breast cancer-specific survival, and recurrence-free survival, HER2-low patients might experience an enhanced prognosis. However, the results did not exhibit statistically significant. The sensitivity analysis confirmed the robustness of the meta-analysis results. No publication bias existed in studies on each outcome indicator.
Conclusion:
HER2 status is essential for the prognostic assessment of TNBC patients, particularly in predicting pCR and OS outcomes.
Systematic Review Registration:
https://www.crd.york.ac.uk/prospero/, identifier PROSPERO CRD-420250642369.
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