Drug intelligence / Profile preview

cyclophosphamide + docetaxel + epirubicin + fluorouracil + pertuzumab + trastuzumab

Development stage
Unknown
Lead developer
Roche
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral, Subcutaneous
01

Overview

This is a multi-agent combination chemotherapy and targeted therapy regimen used primarily for the treatment of HER2-positive breast cancer. The regimen includes: - Cyclophosphamide (an alkylating agent) - Docetaxel (a taxane-class microtubule inhibitor) - Epirubicin (an anthracycline antibiotic, DNA intercalator and topoisomerase II inhibitor) - Fluorouracil (5-FU, a pyrimidine analog antimetabolite inhibiting thymidylate synthase) - Pertuzumab and Trastuzumab (both monoclonal antibodies targeting the human epidermal growth factor receptor 2 [HER2], but binding to different domains). The combination leverages cytotoxic chemotherapy agents with dual HER2 blockade by pertuzumab and trastuzumab, which bind to distinct epitopes on the HER2 receptor. This approach inhibits tumor cell proliferation via direct cytotoxicity, disruption of HER2 signaling pathways, antibody-dependent cellular cytotoxicity, and prevention of receptor dimerization. This regimen is typically used in neoadjuvant or adjuvant settings for early-stage or locally advanced HER2-positive breast cancer as well as in metastatic disease[1][3][5][7].

02

Targets

TS (Thymidylate synthase)HER2 ECD II (Human epidermal growth factor receptor 2 domain II)TOP2A (DNA topoisomerase II)DNA

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