Androgen Receptor in Stage I-II Primary Breast Cancer -Prognostic Value and Distribution in Subgroups
(2017) In Anticancer research 37(12). p.6845-6853- Abstract
BACKGROUND/AIM: The value of androgen receptor (AR) in breast cancer has gained renewed interest as a prognostic and treatment predictive biomarker. The aims of this work were to study the associations and the prognostic value of AR in patients from two clinical cohorts.
MATERIALS AND METHODS: Cohort 1 included 208 premenopausal, node-negative patients of whom 87% had received no adjuvant medical treatment; cohort 2 consisted of 263 patients with stage II disease who had all received 2 years of adjuvant tamoxifen. A semi-quantitative assessment of nuclear AR expression divided into five groups (0-1%, 2-10%, 11-50%, 51-75%, and 76-100%) was performed. Survival analyses, stratified by cohort, were performed using both a trend-test... (More)
BACKGROUND/AIM: The value of androgen receptor (AR) in breast cancer has gained renewed interest as a prognostic and treatment predictive biomarker. The aims of this work were to study the associations and the prognostic value of AR in patients from two clinical cohorts.
MATERIALS AND METHODS: Cohort 1 included 208 premenopausal, node-negative patients of whom 87% had received no adjuvant medical treatment; cohort 2 consisted of 263 patients with stage II disease who had all received 2 years of adjuvant tamoxifen. A semi-quantitative assessment of nuclear AR expression divided into five groups (0-1%, 2-10%, 11-50%, 51-75%, and 76-100%) was performed. Survival analyses, stratified by cohort, were performed using both a trend-test and a cut-off of >10% for positivity.
RESULTS: A total of 76% of all patients were AR+, and 89%, 48%, and 23% of the estrogen receptor-positive, negative, and triple-negative, respectively. In Cox regression, stratified by cohort, AR divided into five groups was a prognostic factor for 5-year distant disease-free survival with a hazard ratio of 0.86 per step in fraction score (p=0.018). With a predefined cut-off at 10%, moderate evidence of an effect remained (Hazard Ratio=0.67, p=0.077). In multivariable analysis, AR did not retain an independent prognostic value.
CONCLUSION: AR is a weak, however, not independent prognostic factor for distant metastasis. Although the prognostic value of AR may be questionable, the study identified a subset of AR-positive triple-negative patients as being potential candidates for AR-directed therapy for which further studies are warranted.
(Less)
- author
- Niméus, Emma
LU
; Folkesson, Elin
LU
; Nodin, Björn
LU
; Hartman, Linda
LU
and Klintman, Marie LU
- organization
-
- Breast cancer Proteogenomics (research group)
- Breast Cancer Surgery (research group)
- Breastcancer-genetics
- BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
- Rheumatology
- Lund OsteoArthritis Division - Clinical Epidemiology Unit (research group)
- Molecular Skeletal Biology (research group)
- Tumor microenvironment
- Personalized Pathology & Cancer Therapy (research group)
- Personalized Breast Cancer Treatment (research group)
- publishing date
- 2017-12-01
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Androgen receptor status, breast cancer, endocrine treatment, prognosis, steroid receptors
- in
- Anticancer research
- volume
- 37
- issue
- 12
- pages
- 9 pages
- publisher
- International Institute of Cancer Research
- external identifiers
-
- pmid:29187464
- wos:000417022100041
- scopus:85038130016
- ISSN
- 1791-7530
- DOI
- 10.21873/anticanres.12146
- language
- English
- LU publication?
- yes
- id
- 440ce85f-649d-4313-8a49-3b503c733b74
- date added to LUP
- 2018-01-10 16:27:35
- date last changed
- 2025-01-08 02:39:53
@article{440ce85f-649d-4313-8a49-3b503c733b74, abstract = {{<p>BACKGROUND/AIM: The value of androgen receptor (AR) in breast cancer has gained renewed interest as a prognostic and treatment predictive biomarker. The aims of this work were to study the associations and the prognostic value of AR in patients from two clinical cohorts.</p><p>MATERIALS AND METHODS: Cohort 1 included 208 premenopausal, node-negative patients of whom 87% had received no adjuvant medical treatment; cohort 2 consisted of 263 patients with stage II disease who had all received 2 years of adjuvant tamoxifen. A semi-quantitative assessment of nuclear AR expression divided into five groups (0-1%, 2-10%, 11-50%, 51-75%, and 76-100%) was performed. Survival analyses, stratified by cohort, were performed using both a trend-test and a cut-off of >10% for positivity.</p><p>RESULTS: A total of 76% of all patients were AR+, and 89%, 48%, and 23% of the estrogen receptor-positive, negative, and triple-negative, respectively. In Cox regression, stratified by cohort, AR divided into five groups was a prognostic factor for 5-year distant disease-free survival with a hazard ratio of 0.86 per step in fraction score (p=0.018). With a predefined cut-off at 10%, moderate evidence of an effect remained (Hazard Ratio=0.67, p=0.077). In multivariable analysis, AR did not retain an independent prognostic value.</p><p>CONCLUSION: AR is a weak, however, not independent prognostic factor for distant metastasis. Although the prognostic value of AR may be questionable, the study identified a subset of AR-positive triple-negative patients as being potential candidates for AR-directed therapy for which further studies are warranted.</p>}}, author = {{Niméus, Emma and Folkesson, Elin and Nodin, Björn and Hartman, Linda and Klintman, Marie}}, issn = {{1791-7530}}, keywords = {{Androgen receptor status; breast cancer; endocrine treatment; prognosis; steroid receptors}}, language = {{eng}}, month = {{12}}, number = {{12}}, pages = {{6845--6853}}, publisher = {{International Institute of Cancer Research}}, series = {{Anticancer research}}, title = {{Androgen Receptor in Stage I-II Primary Breast Cancer -Prognostic Value and Distribution in Subgroups}}, url = {{http://dx.doi.org/10.21873/anticanres.12146}}, doi = {{10.21873/anticanres.12146}}, volume = {{37}}, year = {{2017}}, }