Indication

Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer

Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer is a localized malignancy of the mammary epithelium characterized by the expression of estrogen and/or progesterone receptors without overexpression or amplification of the human epidermal growth factor receptor 2 protein. Read more about Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer

4 drugs 3 manufacturers

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Drugs that treat it

Common Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer therapies.

Showing 1–4 of 4 drugs

KISQALI (ribociclib succinate)

ANTINEOPLASTIC- CYCLIN-DEPENDENT KINASE (CDK) 4/6 INHIBITORS·HORMONE RECEPTOR (HR)-POSITIVE, HER2-NEGATIVE ADVANCED BREAST CANCER·+1
Novartis Pharmaceuticals

VERZENIO (abemaciclib)

ANTINEOPLASTIC- CYCLIN-DEPENDENT KINASE (CDK) 4/6 INHIBITORS·HORMONE RECEPTOR (HR)-POSITIVE, HER2-NEGATIVE ADVANCED BREAST CANCER·+2
Eli Lilly and Company

KISQALI (ribociclib succinate)

ANTINEOPLASTIC- CYCLIN-DEPENDENT KINASE (CDK) 4/6 INHIBITORS·HORMONE RECEPTOR (HR)-POSITIVE, HER2-NEGATIVE ADVANCED BREAST CANCER·+1
Novartis Pharmaceuticals
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About Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer.

Hormone receptor (HR)-positive, HER2-negative early-stage breast cancer is a localized malignancy of the mammary epithelium characterized by the expression of estrogen and/or progesterone receptors without overexpression or amplification of the human epidermal growth factor receptor 2 protein.

Representing the most prevalent subtype of breast cancer, it typically affects adult female breast tissue, though it can also occur in males.

Pathophysiologically, tumor cell proliferation is primarily driven by hormone-receptor signaling pathways while remaining confined to the breast and regional lymph nodes (stages I through III) without distant metastatic spread.

Although generally characterized by favorable initial prognoses, this clinical subtype retains a persistent risk of late locoregional or distant recurrence over decades, often influenced by tumor grade, nodal burden, and genomic risk profiles.

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