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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

2533 - Only estrogen receptor “Positive” is not enough to predict the prognosis of breast cancer Running head: Revisiting estrogen positive tumors in 8th AJCC staging era

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Staging Procedures

Tumour Site

Breast Cancer

Presenters

Jai Min Ryu

Citation

Annals of Oncology (2018) 29 (suppl_8): viii14-viii57. 10.1093/annonc/mdy269

Authors

J.M. Ryu1, S.K. Lee1, J.E. Lee1, S.J. Nam2, J. Yu1, H.J. Choi2, I. Kim2, S.W. Kim1

Author affiliations

  • 1 Department Of Surgery, Samsung Medical Center Sungkyunkwan University School of Medicine, 135-710 - Seoul/KR
  • 2 Breast Surgery, Samsung Medical Center Sungkyunkwan University School of Medicine, 135-710 - Seoul/KR

Resources

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Abstract 2533

Background

Beginning in 2018, biomarkers including estrogen receptor (ER) status were incorporated in the 8th AJCC staging system. ER expression levels were not considered in these changes. We hypothesized that the levels of ER expression could affect the prognosis of breast cancer.

Methods

A retrospective review was conducted to identify all female patients with invasive breast cancer between 2003 and 2012. ER negative (group I), weakly ER-positive (group II), and strongly ER-positive (group III) were defined as Allred total scores of 0-2, 3-5, and 6-8, respectively. We examined a multigene panel, designated the BCT score, which is a newly developed prognostic model for predicting the risk of a distant metastasis.

Results

Among the 4,949 patients enrolled in this study, 1,310 (26.5%), 361 (7.3%), and 3,277 (66.2%) were categorized as group I, II, and III, respectively. Median F/U duration was 57.8 months. Compared to group III, patients in group II were younger, had larger tumors, and were also more likely to have PR-negative tumors, HER-2 amplification, high Ki-67, and high nuclear grade. Between group II and III, there was a significant difference in OS (P = 0.0764, .909, and 0.010, respectively). After adjusting for additional factors that may affect OS, the HR for OS showed higher in group II than in group III. The baseline median BCT score indicated that lower ER expression was associated with significantly higher BCT score (P < 0.0001) and significantly more likely to have high risk group (P < 0.0001) relative to higher levels of ER expression group.

Conclusions

ER expression levels affect the prognosis of breast cancer. The risk for patients with weakly ER-positive breast cancer should not be underestimated.

Clinical trial identification

Legal entity responsible for the study

Institutional Review Board (IRB) of Samsung Medical Center in Seoul, Korea (IRB number: 2017-06-130).

Funding

This research was supported by Samsung Medical Center grant (SMO1170021) and by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HI17C1142).

Editorial Acknowledgement

This research was supported by Samsung Medical Center grant (SMO1170021) and by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HI17C1142).

Disclosure

All authors have declared no conflicts of interest.

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