Drug intelligence / Profile preview

docetaxel + epirubicin + fluorouracil

Development stage
Unknown
Lead developer
Sanofi
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

This is a combination chemotherapy regimen consisting of three cytotoxic agents—docetaxel, epirubicin, and fluorouracil. Each drug has a distinct mechanism of action targeting rapidly dividing cancer cells. Docetaxel is a taxane that stabilizes microtubules and inhibits cell division; epirubicin is an anthracycline that intercalates DNA and inhibits topoisomerase II; and fluorouracil (5-FU) is an antimetabolite that interferes with DNA synthesis by inhibiting thymidylate synthase. This combination has been studied primarily in the treatment of breast cancer as neoadjuvant or adjuvant therapy for early-stage or locally advanced disease. It may also be considered in other solid tumors where these agents are individually active.

Other names
docetaxelepirubicinfluorouracil
02

Targets

TUBB (Tubulin (alpha and beta subunits))TS (Thymidylate synthase)TOP2A (DNA topoisomerase II)

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