Drug intelligence / Profile preview

cyclophosphamide + doxorubicin + ftorafur

Development stage
Unknown
Lead developer
Takeda
Modality
Small Molecules
Administration
Intravenous, Oral
01

Overview

This drug is a combination chemotherapy regimen consisting of cyclophosphamide, doxorubicin, and ftorafur. Cyclophosphamide is an alkylating agent that interferes with DNA replication and RNA transcription by cross-linking DNA strands. Doxorubicin is an anthracycline antibiotic that intercalates into DNA, inhibits topoisomerase II, and generates free radicals leading to cytotoxicity. Ftorafur (also known as tegafur) is a prodrug of 5-fluorouracil (5-FU), an antimetabolite that inhibits thymidylate synthase and disrupts DNA synthesis in rapidly dividing cells. This combination has been studied for the treatment of advanced or recurrent breast cancer as well as other solid tumors[6]. The regimen aims to maximize antitumor efficacy by combining agents with different mechanisms of action.

Other names
CAF (when using fluorouracil instead of ftorafur)CAU (when using uracil and tegafur, which is a prodrug of ftorafur)CAUT (with tamoxifen added)
02

Targets

TOP2A (DNA topoisomerase II)DNATS (Thymidylate synthase)

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