drugset / Trial / NCT01528618

Effect and Safety Study of GP/FP Regimens in Advanced Nasopharyngeal Carcinoma

NCT01528618 ↗

Phase 3 Completed 362 enrolled Sun Yat-sen University
RandomizedParallel-groupOpen-labelTreatment

Summary

The present study will be a randomized, control, multicenter phase III study of recurrent or metastatic (R/M) nasopharyngeal carcinoma (NPC) treated with Gemcitabine (Gemzar, Lilly) and cisplatin regimen (GP) or 5-Fluorouracil plus cisplatin regimen (FP). The population consists of recurrent or metastatic nasopharyngeal carcinoma (NPC) that failed the radical radiotherapy or chemotherapy-naïve advanced NPC (stage IV). The effectiveness and side effects will be evaluated according to Standard WHO response criteria and NCI-CTC AE V3.0.

Timeline

Start
2012-02-21
Primary completion
2016-04-10
Completion
2020-12-20

Outcome

Met primary endpoint

paper reported significant progression-free survival improvement with gemcitabine plus cisplatin (GP) versus fluorouracil plus cisplatin PMID 34379443 ↗

paper The median progression-free survival was 7·0 months (4·4-10·9) in the gemcitabine group and 5·6 months (3·0-7·0) in the fluorouracil group (hazard ratio [HR] 0·55 PMID 27567279 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cisplatin Other / unclassified 80 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous
Comparator fluorouracil Small molecule 1000 mg/m2 Intravenous