Literature DB >> 24183366

Changes in ER, PR and HER2 receptors status after neoadjuvant chemotherapy in breast cancer.

Yu-Feng Yang1, Ying-Yang Liao, Le-Qun Li, Shu-Rui Xie, Yan-Fang Xie, Ning-Fu Peng.   

Abstract

Previous studies have reported conflicting results regarding the impact of neoadjuvant chemotherapy (NAC) on estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2) status in breast cancer. Our aim was to investigate whether NAC induces some selective change in the breast biomarkers. We retrospectively detected the immunohistochemical results of ER, PR and HER2 between the core biopsy and surgical excision specimens in 113 patients with NAC. As a control group, we analyzed sample pairs from 102 patients without NAC. Fourteen (12.4%) of 113 patients undergoing NAC showed the ER status modulation in the surgically removed specimen as compared with only 4 (3.9%) of 102 women without NAC (p=0.025). Eighteen (15.9%) of 113 patients given NAC appeared in the PR status alteration in the final surgical specimen, whereas only 7 (6.9%) of 102 patients without NAC did (p=0.038). The HER2 status shift was found in 17 (15.0%) of 113 patients with NAC and in 6 (5.9%) of 102 patients without NAC, respectively (p=0.030). Neoadjuvant chemotherapy does change ER, PR and HER2 status in a statistically significant manner. Retesting these biomarkers of the residual tumor should be considered to improve future tailored adjuvant therapies.
Copyright © 2013 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Breast cancer; Estrogen receptor; Human epidermal growth factor receptor 2; Neoadjuvant chemotherapy; Progesterone receptor

Mesh:

Substances:

Year:  2013        PMID: 24183366     DOI: 10.1016/j.prp.2013.08.012

Source DB:  PubMed          Journal:  Pathol Res Pract        ISSN: 0344-0338            Impact factor:   3.250


  15 in total

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10.  Tumor biomarker conversion between primary and metastatic breast cancer: mRNA assessment and its concordance with immunohistochemistry.

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Journal:  Oncotarget       Date:  2017-05-19
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