Impact of Nuclear Oestrogen Receptor Beta Expression in Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy

Author:

Heitz Florian12,Kümmel Sherko3,Lederer Bianca4,Solbach Christine5,Engels Knut6,Ataseven Beyhan17,Sinn Bruno89,Blohmer Jens Uwe2,Denkert Carsten8910,Barinoff Jana2,Fisseler-Eckhoff Annette11,Loibl Sibylle412

Affiliation:

1. Department of Gynaecology and Gynaecologic Oncology, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Essen, Germany

2. Department of Gynaecology and Gynaecologic Oncology, Charité University, Berlin, Germany

3. Breast Unit, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Essen, Germany

4. German Breast Group (GBG), Neu-Isenburg, Germany

5. Department of Gynaecology and Obstetrics, Goethe University, Frankfurt, Germany

6. Center for Pathology, Cytology and Molecular Pathology, Neuss, Germany

7. Department of Obstetrics and Gynaecology, University Hospital, LMU München, München, Germany

8. Institute of Pathology, Charité University, Berlin, Germany

9. German Cancer Consortium (DKTK), Berlin, Germany

10. Institut für Pathologie, UKGM – Universitätsklinikum Marburg, Philipps-Universität Marburg, Marburg, Germany

11. Department of Pathology, Dr. Horst Schmidt Kliniken Wiesbaden, Wiesbaden, Germany

12. Senologic Oncology, Düsseldorf, Germany

Abstract

Abstract Introduction Oestrogen receptor beta (ER-β) is abundantly expressed in breast cancer (BC), but its impact on neoadjuvant chemotherapy outcome is unknown. Patients and Methods Patients treated in the neoadjuvant GeparTrio trial with available tissue for immunohistochemical analyses were included. Nuclear ER-β expression was correlated with clinico-pathologic characteristics. The impact of its expression on pathological complete response (pCR [ypT0/ypN0]) and survival was determined. Results Samples of 570 patients were available. Low nuclear ER-β expression (IRS < 9) was observed in 48.4% of hormone receptor positive and 58.6% of hormone receptor negative tumours. Low nuclear ER-β expression was associated with higher pCR rates compared to high nuclear ER-β expression (16.1% vs. 4.7%, p = 0.026). Low ER-β expression was no independent predictor of pCR in multivariate analyses. Disease-free and overall survival were not statistically different between patients with high and low nuclear ER-β expression. Triple-negative BCs showed low nuclear ER-β expression in 57.7%, and pCR rates were 27.1% and 0% (p = 0.23) in low and high ER-β expressing tumours, respectively. Conclusion Low ER-β expression is associated with improved pCR rates in univariate analyses. However multivariate analyses and survival analyses do not indicate an impact of ER-β on survival in patients undergoing neoadjuvant chemotherapy. Further examination of ER-β as predictor for endocrine therapy might be of value.

Publisher

Georg Thieme Verlag KG

Subject

Maternity and Midwifery,Obstetrics and Gynecology

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