Estrogen receptor-positive (ER+) breast cancer is the most common form of breast cancer. Antiestrogens were the first therapy aimed at treating this subtype, but resistance to these warranted the development of a new treatment option. CDK4/6 inhibitors address this problem by halting cell cycle progression in ER+ cells, and have proven to be successful in the clinic. Unfortunately, both intrinsic and acquired resistance to CDK4/6 inhibitors are common. Numerous mechanisms of how resistance occurs have been identified to date, including the activation of prominent growth signaling pathways, the loss of tumor-suppressive genes, and noncanonical cell cycle function. Many of these have been successfully targeted and demonstrate the ability to o...
About 75% of all breast cancers are hormone receptor-positive (HR+). However, the efficacy of endocr...
CDK4/6 inhibitors are FDA-approved drugs for estrogen receptor-positive (ER+) breast cancer and are ...
CDK4/6 inhibitors combined with endocrine therapy have demonstrated higher antitumor activity than e...
The introduction of CDK4/6 inhibitors (CDK4/6i) in combination with endocrine therapy (ET) has revol...
The cyclin D-CDK4/6 complexes play a pivotal role in controlling the cell cycle. Deregulation in cyc...
Cyclin-dependent kinase (CDK4/6) inhibitors in combination with endocrine therapy are currently the ...
CDK4/6 inhibitors in combination with endocrine therapy have recently become standard-of-care for tr...
Hormone receptor-positive (HR+) breast cancer (BC) constitutes approximately 75% of all breast cance...
Purpose: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are currently used in combination with endo...
The cyclin D/cyclin-dependent kinases 4 and 6 (CDK4/6)–retinoblastoma protein (RB) pathway plays a k...
Abstract Endocrine therapy (ET) with cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) is currently th...
BackgroundCombined targeting of CDK4/6 and ER is now the standard of care for patients with advanced...
ER positive (ER+) and HER2 negative (HER2-) breast cancers are routinely treated based on estrogen d...
Over the past two decades, high sensitivity to HER2-amplified primary breast cancers has been achiev...
ESR1 mutations contribute to endocrine resistance and occur in a high percentage of hormone-receptor...
About 75% of all breast cancers are hormone receptor-positive (HR+). However, the efficacy of endocr...
CDK4/6 inhibitors are FDA-approved drugs for estrogen receptor-positive (ER+) breast cancer and are ...
CDK4/6 inhibitors combined with endocrine therapy have demonstrated higher antitumor activity than e...
The introduction of CDK4/6 inhibitors (CDK4/6i) in combination with endocrine therapy (ET) has revol...
The cyclin D-CDK4/6 complexes play a pivotal role in controlling the cell cycle. Deregulation in cyc...
Cyclin-dependent kinase (CDK4/6) inhibitors in combination with endocrine therapy are currently the ...
CDK4/6 inhibitors in combination with endocrine therapy have recently become standard-of-care for tr...
Hormone receptor-positive (HR+) breast cancer (BC) constitutes approximately 75% of all breast cance...
Purpose: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are currently used in combination with endo...
The cyclin D/cyclin-dependent kinases 4 and 6 (CDK4/6)–retinoblastoma protein (RB) pathway plays a k...
Abstract Endocrine therapy (ET) with cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) is currently th...
BackgroundCombined targeting of CDK4/6 and ER is now the standard of care for patients with advanced...
ER positive (ER+) and HER2 negative (HER2-) breast cancers are routinely treated based on estrogen d...
Over the past two decades, high sensitivity to HER2-amplified primary breast cancers has been achiev...
ESR1 mutations contribute to endocrine resistance and occur in a high percentage of hormone-receptor...
About 75% of all breast cancers are hormone receptor-positive (HR+). However, the efficacy of endocr...
CDK4/6 inhibitors are FDA-approved drugs for estrogen receptor-positive (ER+) breast cancer and are ...
CDK4/6 inhibitors combined with endocrine therapy have demonstrated higher antitumor activity than e...