We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD4547 (a potent and selective inhibitor of Fibroblast Growth Factor Receptor (FGFR)-1, 2 and 3 receptor tyrosine kinases) administered with anastrozole or letrozole in estrogen receptor positive metastatic breast cancer patients who had become resistant to aromatase inhibitors. After a safety run-in study to assess safety and tolerability, we recruited 52 patients. The primary endpoint was change in tumour size at 12 weeks, and secondary endpoints were to assess response at 6 weeks, 20 weeks and every 8 weeks thereafter and tolerability of the combined treatment. Two partial responses (PR) and 19 stable disease (SD) patients were observed at the...
Uncontrolled activation of FGFRs induces the progression of various cancers. It was recently reporte...
Background: Overexpression of fibroblast growth factor receptor 1 (FGFR1), found in ≤8% of hormone r...
Hormonal therapy is the preferred systemic treatment for recurrent or metastatic, post-menopausal ho...
We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD45...
We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD45...
Background Preclinical data suggest that epidermal growth factor receptor (EGFR) inhibitors (e.g. ge...
Background:Approximately 5%-10% of gastric cancers have a fibroblast growth factor receptor-2 (FGFR2...
BACKGROUND: The aim of this study was to evaluate the efficacy and tolerability of fulvestrant, an e...
Background: Approximately 5–10% of gastric cancers (GCs) have a fibroblast growth factor receptor-2 ...
Background: The aim of this study was to evaluate the efficacy and tolerability of fulvestrant, an e...
Background Aromatase inhibitors are a standard of care for hormone receptor-positive locally adva...
Introduction: Upregulation of PI3K/Akt/mTOR signalling in endocrine-resistant breast cancer (BC) has...
BACKGROUND: The combined use of a FGFR1 blocker and aromatase inhibitors is appealing for treating b...
Uncontrolled activation of FGFRs induces the progression of various cancers. It was recently reporte...
Background: Overexpression of fibroblast growth factor receptor 1 (FGFR1), found in ≤8% of hormone r...
Hormonal therapy is the preferred systemic treatment for recurrent or metastatic, post-menopausal ho...
We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD45...
We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD45...
Background Preclinical data suggest that epidermal growth factor receptor (EGFR) inhibitors (e.g. ge...
Background:Approximately 5%-10% of gastric cancers have a fibroblast growth factor receptor-2 (FGFR2...
BACKGROUND: The aim of this study was to evaluate the efficacy and tolerability of fulvestrant, an e...
Background: Approximately 5–10% of gastric cancers (GCs) have a fibroblast growth factor receptor-2 ...
Background: The aim of this study was to evaluate the efficacy and tolerability of fulvestrant, an e...
Background Aromatase inhibitors are a standard of care for hormone receptor-positive locally adva...
Introduction: Upregulation of PI3K/Akt/mTOR signalling in endocrine-resistant breast cancer (BC) has...
BACKGROUND: The combined use of a FGFR1 blocker and aromatase inhibitors is appealing for treating b...
Uncontrolled activation of FGFRs induces the progression of various cancers. It was recently reporte...
Background: Overexpression of fibroblast growth factor receptor 1 (FGFR1), found in ≤8% of hormone r...
Hormonal therapy is the preferred systemic treatment for recurrent or metastatic, post-menopausal ho...