drugset / Trial / NCT01561586

Tri-weekly Cisplatin Based Chemoradiation in Locally Advanced Cervical Cancer

NCT01561586 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

Current standard treatment for locally advanced cervical cancer is cisplatin-based concurrent chemoradiation (CRT). Although recently reported meta-analysis studies also demonstrated improved local control rates and survival with cisplatin-based chemotherapy concurrent to radiation therapy (RT), the optimal cisplatin dose and dosing schedule are still undetermined. In light of the results of the previous clinical trial, weekly cisplatin 40 mg/m2 considered to be a standard regiment in cisplatin doses and dosing schedules. However, our randomized phase II trial showed that tri-weekly cisplatin 75mg/m2 has lower toxicities and a better outcome in locally advanced cervical cancer. In this randomized phase III trial, the investigators investigate that there may be a survival difference between weekly cisplatin 40 mg/m2 and tri-weekly cisplatin 75 mg/m2 administration concurrent to RT in cervical cancer.

Timeline

Start
2012-03
Primary completion
2020-03
Completion
2023-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cisplatin Other / unclassified 40 mg/m2 Intravenous
Comparator Cisplatin Other / unclassified 75 mg/m2 Intravenous

Indications