The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormone receptor-positive (HR + ) and human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer, improving survival outcomes compared to endocrine therapy alone. Abemaciclib and ribociclib, in combination with endocrine therapy, have demonstrated significant benefits in invasive disease-free survival for high-risk HR+/HER2- early breast cancer patients. Each CDK4/6i-palbociclib, ribociclib, and abemaciclib-exhibits distinct toxicity profiles. Radiation therapy (RT) can be delivered with a palliative or ablative intent, particularly using stereotactic body radiation therapy for oligometastatic or oligoprogressive disease. Ho...
Purpose: To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 an...
Abstract Uncontrolled cell division is the hallmark of cancers. Full understanding of cell cycle reg...
Background To compare the efficacy and toxicity of the combination of cyclin-dependent kinase 4/6...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
Breast Cancer is the most common type of cancer worldwide. Scientific advances and new ways of treat...
Current first-line systemic treatment in most patients with metastatic hormone receptor-positive, HE...
The addition of CDK4/6 inhibitors to endocrine therapy in advanced hormone receptor-positive HER2-ne...
The emergence of cyclin-dependent kinase (CDK) 4 and 6 inhibitors has brought a new approach in the ...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Abstract Aberrations of the cell cycle are pervasive in cancer, and selective cell cycle inhibition ...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Purpose: To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 an...
Abstract Uncontrolled cell division is the hallmark of cancers. Full understanding of cell cycle reg...
Background To compare the efficacy and toxicity of the combination of cyclin-dependent kinase 4/6...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormon...
Breast Cancer is the most common type of cancer worldwide. Scientific advances and new ways of treat...
Current first-line systemic treatment in most patients with metastatic hormone receptor-positive, HE...
The addition of CDK4/6 inhibitors to endocrine therapy in advanced hormone receptor-positive HER2-ne...
The emergence of cyclin-dependent kinase (CDK) 4 and 6 inhibitors has brought a new approach in the ...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Abstract Aberrations of the cell cycle are pervasive in cancer, and selective cell cycle inhibition ...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Cyclin-dependent kinases (CDK) 4/6 inhibitors, namely abemaciclib, palbociclib, and ribociclib, inte...
Purpose: To provide an overview of clinical data supporting the use of cyclin-dependent kinases 4 an...
Abstract Uncontrolled cell division is the hallmark of cancers. Full understanding of cell cycle reg...
Background To compare the efficacy and toxicity of the combination of cyclin-dependent kinase 4/6...