Drug intelligence / Profile preview

fluorouracil + epirubicin + cyclophosphamide followed by docetaxel + trastuzumab

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

Overview

This regimen is a sequential combination chemotherapy protocol used primarily for the treatment of HER2-positive breast cancer. It consists of an initial phase with fluorouracil (5-FU), epirubicin, and cyclophosphamide (commonly referred to as FEC), followed by a second phase with docetaxel and trastuzumab. - **Fluorouracil** is an antimetabolite that inhibits thymidylate synthase, disrupting DNA synthesis. - **Epirubicin** is an anthracycline antibiotic that intercalates into DNA and inhibits topoisomerase II. - **Cyclophosphamide** is an alkylating agent causing cross-linking of DNA strands. - **Docetaxel** is a taxane that stabilizes microtubules, inhibiting cell division. - **Trastuzumab** is a monoclonal antibody targeting the human epidermal growth factor receptor 2 (HER2/neu), blocking its signaling and mediating antibody-dependent cellular cytotoxicity. This regimen leverages both cytotoxic chemotherapy and targeted therapy to maximize efficacy in HER2-positive breast cancer patients. The addition of trastuzumab to chemotherapy has been shown to improve response rates, progression-free survival, and overall survival in this population[2][6][8][9].

Other names
FEC followed by docetaxel and trastuzumabFEC-D+TFEC-D plus trastuzumab
02

Targets

TS (Thymidylate synthase)TOP2A (DNA topoisomerase II)ERBB2 (Erb-b2 receptor tyrosine kinase 2)DNATUBB (Tubulin (alpha and beta subunits))

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