AbstractBackgroundIn 2007 the St. Gallen consensus panel defined three endocrine response classes: highly endocrine responsive (ER-H), incomplete endocrine responsive (ER-I) and non-endocrine responsive tumours (ER-N). However, it is uncertain whether ER-I tumours are less responsive than ER-H tumours. We investigated whether recurrence rates vary over time between response classes. Additionally, we investigated the most predictive response class definition for tamoxifen benefit.Patients and methodsWe recollected tumours from 646 patients who participated in a randomized trial of adjuvant tamoxifen vs. observation. Estrogen receptor (ER), progesterone receptor (PgR), HER2 status and tumour grade were revised centrally. St. Gallen classes we...
Background Understanding how tumor response is related to relapse risk would help clinicians make de...
Importance:Multiple molecular signatures are available for managing estrogen receptor (ER)-positive ...
Background: Endocrine sensitivity, as determined by response of the proliferation marker Ki-67 to sh...
BACKGROUND: In 2007 the St. Gallen consensus panel defined three endocrine response classes: highly ...
Extended endocrine therapy can reduce recurrences occurring more than 5 years after diagnosis (late ...
This article is distributed under the terms of the Creative Commons Attribution 4.0 International L...
Breast cancer (BC) exhibits great heterogeneity at histophatological, clinical and molecular levels....
The current therapeutic strategy in breast cancer is to identify a target, such as estrogen receptor...
Background: The 21-gene recurrence score (RS) predicts risk of locoregional recurrence (LRR) in node...
Background: Aromatase inhibitors improve disease-free survival compared with tamoxifen in postmenop...
Background: The role of adjuvant dose-intensive chemotherapy and its efficacy according to baseline ...
Background: The benefit of adjuvant chemotherapy in postmenopausal patients with estrogen receptor (...
Background: Aromatase inhibitors improve disease-free survival compared with tamoxifen in postmenopa...
Background: The role of chemotherapy in addition to combined endocrine therapy for premenopausal wom...
Background Estimating distant recurrence (DR) risk among women with estrogen receptor-positive (ER+)...
Background Understanding how tumor response is related to relapse risk would help clinicians make de...
Importance:Multiple molecular signatures are available for managing estrogen receptor (ER)-positive ...
Background: Endocrine sensitivity, as determined by response of the proliferation marker Ki-67 to sh...
BACKGROUND: In 2007 the St. Gallen consensus panel defined three endocrine response classes: highly ...
Extended endocrine therapy can reduce recurrences occurring more than 5 years after diagnosis (late ...
This article is distributed under the terms of the Creative Commons Attribution 4.0 International L...
Breast cancer (BC) exhibits great heterogeneity at histophatological, clinical and molecular levels....
The current therapeutic strategy in breast cancer is to identify a target, such as estrogen receptor...
Background: The 21-gene recurrence score (RS) predicts risk of locoregional recurrence (LRR) in node...
Background: Aromatase inhibitors improve disease-free survival compared with tamoxifen in postmenop...
Background: The role of adjuvant dose-intensive chemotherapy and its efficacy according to baseline ...
Background: The benefit of adjuvant chemotherapy in postmenopausal patients with estrogen receptor (...
Background: Aromatase inhibitors improve disease-free survival compared with tamoxifen in postmenopa...
Background: The role of chemotherapy in addition to combined endocrine therapy for premenopausal wom...
Background Estimating distant recurrence (DR) risk among women with estrogen receptor-positive (ER+)...
Background Understanding how tumor response is related to relapse risk would help clinicians make de...
Importance:Multiple molecular signatures are available for managing estrogen receptor (ER)-positive ...
Background: Endocrine sensitivity, as determined by response of the proliferation marker Ki-67 to sh...