Cyclin-dependent kinase (CDK4/6) inhibitors in combination with endocrine therapy are currently the optimal first line treatment for hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) non-amplified metastatic breast cancer (MBC). However, not all patients benefit from this treatment and all patients will inevitably progress. Identifying therapeutic strategies in this setting is therefore of immediate clinical importance. We present an overview of the mechanisms of resistance to CDK4/6 inhibitors and review potential biomarkers that may guide therapy selection. We also discuss the use of CDK4/6 inhibitors in the context of non-HR-positive/HER2-non-amplified breast cancer and in combination with therapies other th...
Purpose: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are currently used in combination with endo...
Advanced hormone receptor-positive breast cancer is one of the women’s most common malignant disease...
Over the past two decades, high sensitivity to HER2-amplified primary breast cancers has been achiev...
Resistance to endocrine therapy is a significant therapeutic challenge in the treatment of women wit...
The development of cyclin-dependent kinase (CDK) 4/6 inhibitors has been more prominent in hormone r...
Estrogen receptor-positive (ER+) breast cancer is the most common form of breast cancer. Antiestroge...
The introduction of CDK4/6 inhibitors (CDK4/6i) in combination with endocrine therapy (ET) has revol...
In the last 3 years, a novel class of targeted therapy has been approved for patients with hormone r...
Abstract Endocrine therapy (ET) with cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) is currently th...
The cyclin D-CDK4/6 complexes play a pivotal role in controlling the cell cycle. Deregulation in cyc...
About 75% of all breast cancers are hormone receptor-positive (HR+). However, the efficacy of endocr...
Hormone receptor-positive (HR+) breast cancer (BC) constitutes approximately 75% of all breast cance...
Dysregulation of the cyclin D and cyclin-dependent kinase (CDK) pathway in cancer cells may inhibit ...
Purpose: To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 an...
The cyclin D/cyclin-dependent kinases 4 and 6 (CDK4/6)–retinoblastoma protein (RB) pathway plays a k...
Purpose: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are currently used in combination with endo...
Advanced hormone receptor-positive breast cancer is one of the women’s most common malignant disease...
Over the past two decades, high sensitivity to HER2-amplified primary breast cancers has been achiev...
Resistance to endocrine therapy is a significant therapeutic challenge in the treatment of women wit...
The development of cyclin-dependent kinase (CDK) 4/6 inhibitors has been more prominent in hormone r...
Estrogen receptor-positive (ER+) breast cancer is the most common form of breast cancer. Antiestroge...
The introduction of CDK4/6 inhibitors (CDK4/6i) in combination with endocrine therapy (ET) has revol...
In the last 3 years, a novel class of targeted therapy has been approved for patients with hormone r...
Abstract Endocrine therapy (ET) with cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) is currently th...
The cyclin D-CDK4/6 complexes play a pivotal role in controlling the cell cycle. Deregulation in cyc...
About 75% of all breast cancers are hormone receptor-positive (HR+). However, the efficacy of endocr...
Hormone receptor-positive (HR+) breast cancer (BC) constitutes approximately 75% of all breast cance...
Dysregulation of the cyclin D and cyclin-dependent kinase (CDK) pathway in cancer cells may inhibit ...
Purpose: To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 an...
The cyclin D/cyclin-dependent kinases 4 and 6 (CDK4/6)–retinoblastoma protein (RB) pathway plays a k...
Purpose: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are currently used in combination with endo...
Advanced hormone receptor-positive breast cancer is one of the women’s most common malignant disease...
Over the past two decades, high sensitivity to HER2-amplified primary breast cancers has been achiev...