drugset / Trial / NCT00273546

Induction Chemotherapy Comparing Taxotere® Cisplatin and 5-Fluorouracil (TPF) With Standard Cisplatin and 5-Fluorouracil (PF) Followed by Chemoradiation in Locally Advanced Head and Neck Cancer

NCT00273546 ↗

Phase 3 Completed 500 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

* 1.To compare overall survival after treatment with the test tri-therapy (TPF: docetaxel plus cisplatin and 5FU) or the control treatment (PF: cisplatin plus 5-FU) followed by chemoradiotherapy in patients with locally advanced SCCHN. * 2.The main secondary endpoint is progression free survival (PFS). The other secondary endpoints are to evaluate and compare improvement of local symptoms; time-to-treatment failure; quality of life; clinical complete response rate (CR and CR/PR); toxicity and to evaluate the relationship of tumor markers and response to therapy.

Timeline

Start
1999-05
Primary completion
2006-02
Completion
2006-02

Outcome

Met primary endpoint

paper significantly more patients survived in the TPF group than in the PF group (hazard ratio for death, 0.70; P=0.006). PMID 17960013 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2 —

Indications