Arsenic Trioxide in Treating Patients With Metastatic Liver Cancer That Cannot Be Removed by Surgery
Liver Cancer
About this trial
This is an interventional treatment trial for Liver Cancer focused on measuring adult primary hepatocellular carcinoma, advanced adult primary liver cancer, recurrent adult primary liver cancer
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed hepatocellular carcinoma Unresectable metastatic disease Ascites allowed provided it is minimal PATIENT CHARACTERISTICS: Age Over 18 Performance status 0-2 Life expectancy Not specified Hematopoietic WBC > 2,500/mm^3 Absolute neutrophil count > 1,500/mm^3 Platelet count > 75,000/mm^3 Hepatic Bilirubin < 2.5 mg/dL AST < 2.5 times upper limit of normal Renal Not specified Cardiovascular QTc interval ≤ 460 msec AND potassium and magnesium normal Other Not pregnant or nursing Negative pregnancy test Fertile female patients must use effective double-method contraception for ≥ 4 weeks before, during, and for ≥ 4 weeks after completion of study treatment (during and for ≥ 4 weeks after completion of study treatment for male patients) No blood, ova, or sperm donation during study treatment Potassium > 4.0 mEq/dL Magnesium > 1.8 mg/dL PRIOR CONCURRENT THERAPY: Biologic therapy No concurrent biologic therapy Chemotherapy More than 4 weeks since prior and no other concurrent chemotherapy Endocrine therapy Not specified Radiotherapy More than 4 weeks since prior and no concurrent radiotherapy Surgery Not specified Other No other concurrent investigational agents
Sites / Locations
- UPMC Cancer Centers