Indication
Hormone receptor (HR)-positive, HER2-negative advanced breast cancer
Hormone receptor (HR)-positive, HER2-negative advanced breast cancer refers to a malignancy originating in mammary tissue that has progressed to locally advanced, unresectable disease or disseminated to distant metastatic sites. Read more about Hormone receptor (HR)-positive, HER2-negative advanced breast cancer
8 drugs 7 manufacturers
Drugs that treat it
Common Hormone receptor (HR)-positive, HER2-negative advanced breast cancer therapies.
KISQALI (ribociclib succinate)
KISQALI FEMARA CO-PACK (ribociclib succinate/letrozole)
VERZENIO (abemaciclib)
TRODELVY (sacituzumab govitecan-hziy)
TRODELVY (sacituzumab govitecan-hziy)
DATROWAY (datopotamab deruxtecan-dlnk)
KISQALI (ribociclib succinate)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonHormone receptor (HR)-positive, HER2-negative advanced breast cancer refers to a malignancy originating in mammary tissue that has progressed to locally advanced, unresectable disease or disseminated to distant metastatic sites.
Pathophysiologically, tumor cells demonstrate significant expression of estrogen and/or progesterone receptors—which serve as principal intracellular drivers of oncogenic signaling and proliferation—while lacking human epidermal growth factor receptor 2 gene amplification or protein overexpression.
This clinical presentation predominantly affects adult women, though it may also occur in men, and represents the most prevalent biological subtype of advanced mammary carcinoma.
Clinically, it reflects an incurable yet treatable chronic oncologic state characterized by systemic disease burden and variable sensitivity or acquired resistance to endocrine-based therapies.
- cancer.gov
Hormone receptor (HR)-positive, HER2-negative advanced breast cancer refers to a malignancy originating in mammary tissue that has progressed to locally advanced, unresectable disease or disseminated to distant metastatic sites Pathophysiologically, tumor cells demonstrate significant expression of estrogen and/or progesterone receptors—which serve as principal intracellular drivers of oncogenic signaling and proliferation—while lacking human epidermal growth factor receptor 2 gene amplification...
- nih.gov
Hormone receptor (HR)-positive, HER2-negative advanced breast cancer refers to a malignancy originating in mammary tissue that has progressed to locally advanced, unresectable disease or disseminated to distant metastatic sites This clinical presentation predominantly affects adult women, though it may also occur in men, and represents the most prevalent biological subtype of advanced mammary carcinoma Clinically, it reflects an incurable yet treatable chronic oncologic state characterized by sy...
- cancer.gov
Hormone receptor (HR)-positive, HER2-negative advanced breast cancer refers to a malignancy originating in mammary tissue that has progressed to locally advanced, unresectable disease or disseminated to distant metastatic sites
- cancer.gov
Pathophysiologically, tumor cells demonstrate significant expression of estrogen and/or progesterone receptors—which serve as principal intracellular drivers of oncogenic signaling and proliferation—while lacking human epidermal growth factor receptor 2 gene amplification or protein overexpression
- honcology.com
Pathophysiologically, tumor cells demonstrate significant expression of estrogen and/or progesterone receptors—which serve as principal intracellular drivers of oncogenic signaling and proliferation—while lacking human epidermal growth factor receptor 2 gene amplification or protein overexpression
- clevelandclinic.org
This clinical presentation predominantly affects adult women, though it may also occur in men, and represents the most prevalent biological subtype of advanced mammary carcinoma
- breastcancer.org
This clinical presentation predominantly affects adult women, though it may also occur in men, and represents the most prevalent biological subtype of advanced mammary carcinoma
- healthbooktimes.org
Clinically, it reflects an incurable yet treatable chronic oncologic state characterized by systemic disease burden and variable sensitivity or acquired resistance to endocrine-based therapies
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