BACKGROUND: Breast cancer patients with node positive disease can have an excellent outcome with tamoxifen only. It is unclear whether analysing both the 70-gene signature and hormone receptors provides superior prediction of outcome in tamoxifen-treated patients than either alone. METHODS: Three series were evaluated: 121 patients (81% node positive) received adjuvant tamoxifen, 151 patients did not receive tamoxifen (10% node positive) and 92 patients received tamoxifen for metastatic disease. The 70-gene signature was analysed using MammaPrint. Oestrogen receptor (ER) and progesterone receptor (PR) immunohistochemistry was evaluated following St. Gallen Consensus (Highly Endocrine Responsive: ER and PR >/= 50%, Incompletely Endocrine Res...
BackgroundER-positive (ER+ ) breast cancer includes all of the intrinsic molecular subtypes, althoug...
Introduction Few markers are available that can predict response to tamoxifen treatment in estrogen ...
Breast cancer (BC) exhibits great heterogeneity at histophatological, clinical and molecular levels....
Item does not contain fulltextBACKGROUND: Breast cancer patients with node positive disease can have...
Contains fulltext : 139100.pdf (publisher's version ) (Open Access)To identify mol...
Background Molecular signatures that predict outcome in tamoxifen treated breast cancer patients hav...
BACKGROUND: Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast can...
Background: Estrogen receptor positive (ER+) breast cancers (BC) are heterogeneous with regard to th...
Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast cancer, but the...
Background: Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast can...
BACKGROUND: Estrogen receptor positive (ER+) breast cancers (BC) are heterogeneous with regard to th...
Importance: Multiple molecular signatures are available for managing estrogen receptor (ER)-positive...
PURPOSE: To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups...
Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups ...
Background: Gene signatures including OncotypeDX are under intense study for their prognostic value,...
BackgroundER-positive (ER+ ) breast cancer includes all of the intrinsic molecular subtypes, althoug...
Introduction Few markers are available that can predict response to tamoxifen treatment in estrogen ...
Breast cancer (BC) exhibits great heterogeneity at histophatological, clinical and molecular levels....
Item does not contain fulltextBACKGROUND: Breast cancer patients with node positive disease can have...
Contains fulltext : 139100.pdf (publisher's version ) (Open Access)To identify mol...
Background Molecular signatures that predict outcome in tamoxifen treated breast cancer patients hav...
BACKGROUND: Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast can...
Background: Estrogen receptor positive (ER+) breast cancers (BC) are heterogeneous with regard to th...
Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast cancer, but the...
Background: Tamoxifen significantly improves outcome for estrogen receptor-positive (ER+) breast can...
BACKGROUND: Estrogen receptor positive (ER+) breast cancers (BC) are heterogeneous with regard to th...
Importance: Multiple molecular signatures are available for managing estrogen receptor (ER)-positive...
PURPOSE: To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups...
Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups ...
Background: Gene signatures including OncotypeDX are under intense study for their prognostic value,...
BackgroundER-positive (ER+ ) breast cancer includes all of the intrinsic molecular subtypes, althoug...
Introduction Few markers are available that can predict response to tamoxifen treatment in estrogen ...
Breast cancer (BC) exhibits great heterogeneity at histophatological, clinical and molecular levels....