Drug intelligence / Profile preview

cisplatin + fluorouracil + radiotherapy

Development stage
Phase 4
Lead developer
Sun Yat-sen University
Modality
Small Molecules, Implantable Devices → Device-based Delivery → Drug Delivery Systems
Administration
Intravenous
01

Overview

This therapeutic regimen is designed for the treatment of advanced nasopharyngeal carcinoma (NPC), specifically targeting patients with N2-3 stage disease. The protocol consists of concurrent chemoradiotherapy (CCRT) followed by adjuvant chemotherapy. During the CCRT phase, patients receive concurrent cisplatin (a platinum-based DNA cross-linking agent) alongside intensity-modulated radiotherapy (IMRT). This is followed by an adjuvant chemotherapy phase known as the PF regimen, which combines cisplatin with 5-fluorouracil (5-FU). 5-fluorouracil is a pyrimidine analog antimetabolite that inhibits thymidylate synthase, thereby interfering with DNA synthesis. This specific treatment sequence was evaluated in a Phase 3 clinical trial conducted by Sun Yat-sen University to compare its efficacy and safety against a gemcitabine plus cisplatin (GP) adjuvant regimen.

Other names
cisplatin/5-FU adjuvant therapy after CCRTPF regimenconcurrent chemoradiotherapy followed by adjuvant cisplatin and 5-fluorouracil
02

Targets

TS (Thymidylate synthase)DNA

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