drugset / Trial / NCT00404326

Hydralazine and Valproate Plus Cisplatin Chemoradiation in Cervical Cancer

NCT00404326

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The current standard for locally advanced cervical cancer is concurrent cisplatin-based chemotherapy, however, the treatment results need to be improved. Epigenetic aberrations play an important role in cancer progression by silencing growth regulatory genes and there is now evidence that inhibitors of DNA methylation and HDAC inhibition synergize the radiation and chemotherapy effects. Objective. To determine response rate, safety and biological effects of hydralazine and magnesium valproate when added to cisplatin chemoradiation. Hypothesis. Hydralazine and magnesium valproate associated to chemoradiation will increase the clinical complete response rate to 95% as compared to 75% as seen in historical controls treated with cisplatin chemoradiation in FIGO stage IIIB patients. Metodology. A total of 17 FIGO stage IIIB patients with histologically confirmed cervical carcinoma with no previous treatment will be included. Patients will be typed for acetylator status and and then receive either 182 or 83 mg of hydralazine, and magnesium valproate at 40mg/Kg from day -7 to the end of chemoradiation (external and brachytherapy). Clinical response rate, safety and transcriptome changes will be analyzed.

Timeline

Start
2005-05
Primary completion
Completion
2006-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Hydralazine Small molecule 83 mg
Subject Hydralazine Small molecule 182 mg
Subject Valproate Small molecule 30 mg/kg
Subject Valproate Small molecule 40 mg/kg

Indications