Estrogen Receptor Alpha Gene Amplification Is an Independent Predictor of Long-Term Outcome in Postmenopausal Patients with Endocrine-Responsive Early Breast Cancer

Author:

Singer Christian F.1ORCID,Holst Frederik12ORCID,Steurer Stefan2,Burandt Eike C.2ORCID,Lax Sigurd F.345,Jakesz Raimund6,Rudas Margaretha7,Stöger Herbert8,Greil Richard9,Sauter Guido2,Filipits Martin10ORCID,Simon Ronald2ORCID,Gnant Michael11ORCID, , , ,

Affiliation:

1. 1Department of OB/GYN, Medical University of Vienna, Vienna, Austria.

2. 2Department of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

3. 4Department of Pathology, Medical University of Graz, Graz, Austria.

4. 5Hospital Graz II, Graz, Austria.

5. 6Johannes Kepler University, School of Medicine, Graz, Austria.

6. 7Department of Surgery, Medical University of Vienna, Vienna, Austria.

7. 8Department of Pathology, Medical University of Vienna, Vienna, Austria.

8. 3Department of Medicine, Medical University of Graz, Graz, Austria.

9. 9Salzburg Cancer Research Institute - Center for Clinical and Immunology Trials and Cancer Cluster Salzburg; IIIrd Medical Department, Paracelsus Medical University Salzburg, Salzburg, Austria.

10. 10Center for Cancer Research, Medical University of Vienna, Vienna, Austria.

11. 11Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Abstract

Abstract Purpose: Estrogen receptor (ER) expression is a prognostic parameter in breast cancer, and a prerequisite for the use of endocrine therapy. In ER+ early breast cancer, however, no receptor-associated biomarker exists that identifies patients with a particularly favorable outcome. We have investigated the value of ESR1 amplification in predicting the long-term clinical outcome in tamoxifen-treated postmenopausal women with endocrine-responsive breast cancer. Experimental Design: 394 patients who had been randomized into the tamoxifen-only arm of the prospective randomized ABCSG-06 trial of adjuvant endocrine therapy with available formalin-fixed, paraffin-embedded tumor tissue were included in this analysis. IHC ERα expression was evaluated both locally and in a central lab using the Allred score, while ESR1 gene amplification was evaluated by FISH analysis using the ESR1/CEP6 ratio indicating focal copy number alterations. Results: Focal ESR1 copy-number elevations (amplifications) were detected in 187 of 394 (47%) tumor specimens, and were associated with a favorable outcome: After a median follow-up of 10 years, women with intratumoral focal ESR1 amplification had a significantly longer distant recurrence-free survival [adjusted HR, 0.48; 95% confidence interval (CI), 0.26–0.91; P = 0.02] and breast cancer–specific survival (adjusted HR 0.47; 95% CI, 0.27–0.80; P = 0.01) as compared with women without ESR1 amplification. IHC ERα protein expression, evaluated by Allred score, correlated significantly with focal ESR1 amplification (P < 0.0001; χ2 test), but was not prognostic by itself. Conclusions: Focal ESR1 amplification is an independent and powerful predictor for long-term distant recurrence-free and breast cancer–specific survival in postmenopausal women with endocrine-responsive early-stage breast cancer who received tamoxifen for 5 years.

Funder

Deutsche Forschungsgemeinschaft

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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