Definition A malignant tumor that starts in the epithelial lining of the breast’s milk ducts, breaks through the duct wall, and invades the surrounding breast tissue, with potential to metastasize to lymph nodes and distant organs.

Key Features for Oncology/Pharmacy Context

Prognosis Factors

Subtype Key Biomarkers Typical Staging at Dx First-Line Systemic Therapy Key Notes / Pharmacist Considerations
Hormone receptor–positive / HER2-negative ER+, PR+, HER2– Early (I–III) or metastatic Early stage: Surgery ± radiationadjuvant endocrine therapy (tamoxifen or aromatase inhibitor ± CDK4/6 inhibitor in high-risk)
Metastatic: Endocrine therapy + CDK4/6 inhibitor (palbociclib, ribociclib, abemaciclib)
Monitor for endocrine therapy side effects (VTE, menopausal symptoms, bone density). CDK4/6 inhibitors → CBC monitoring for neutropenia.
HER2-positive (any HR status) HER2 overexpression/amplification (IHC 3+ or FISH+) Early (I–III) or metastatic Early stage: Surgery ± radiation → trastuzumab-based regimen (TCHP or AC-THP).
Metastatic: Trastuzumab + pertuzumab + taxane (THP) first-line
Monitor cardiac function (LVEF) for HER2-targeted agents; taxanes → neuropathy risk.
Triple-negative (ER–, PR–, HER2–) All three negative Often higher grade; may be aggressive Early stage: Neoadjuvant chemo (anthracycline + taxane ± carboplatin).
Metastatic: Chemo ± immunotherapy if PD-L1+ (atezolizumab + nab-paclitaxel or pembrolizumab + chemo)
High recurrence risk; immune-related adverse effects with checkpoint inhibitors; manage chemo toxicities aggressively.
Inflammatory breast cancer (any subtype) Variable Usually stage III Neoadjuvant systemic therapy based on receptor status → surgery → radiation Aggressive disease; tight coordination with oncology team for sequence of therapy.
Synonyms
IDC, infiltrating ductal carcinoma
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