Sorafenib Tosylate in Treating Patients With Liver Cancer That Can Be Removed by Surgery

This is an interventional treatment trial for Liver Cancer focused on measuring adult primary hepatocellular carcinoma, localized resectable adult primary liver cancer Read More

DISEASE CHARACTERISTICS:

• Histologically confirmed hepatocellular carcinoma (HCC)

  • Fibrolamellar or mixed histology allowed
  • No cholangiocarcinoma or other tubal disease
• Must be eligible for conservative hepatic resection or liver resection with curative intent
• No cirrhosis with Child-Pugh score > 7
• Chronic liver disease without liver insufficiency and without portal liver hypertension allowed
• No known history or presence of metastatic brain or meningeal tumors

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1
• Life expectancy ≥ 3 months
• WBC > 3,000/µL
• ANC > 1,500/µL
• Platelet count ≥ 100,000/µL
• Hemoglobin ≥ 9 g/dL
• Bilirubin < 1.5 times upper normal limit (ULN)
• AST and ALT ≤ 5 times UNL
• Alkaline phosphatase ≤ 5 times ULN
• Serum creatinine < 2 times ULN
• PT/INR/PTT < 1.5 times UNL
• Amylase and lipase < 1.5 times ULN
• Negative pregnancy test
• Fertile patients must use effective contraception
• Body mass index 18.5-30 kg/m^2 (WHO normal range: 18.5-25 kg/m^2)
• Able to swallow oral compound
• No criterion for unresectability or medical condition that contraindicates surgical resection

• No serious concurrent systemic disorder incompatible with the study, including any of the following:

  • Uncontrolled hypertension (i.e., BP > 150/100 mm Hg despite optimal therapy)
  • Active uncontrolled infection
  • Active alcoholism

• No prior medical disorder, including any of the following:

  • Cardiac arrhythmias requiring anti-arrhythmics (excluding beta-blockers or digoxin for chronic atrial fibrillation)
  • Active coronary artery disease or ischemia
  • Myocardial infarction within the past 6 months
  • NYHA class III-IV congestive heart failure
  • Pulmonary embolism within the past 6 months
  • Gastrointestinal bleeding within the past 6 months
• No other prior malignancy within the past 5 years, except basal cell or squamous cell skin carcinoma or cured in situ cervical carcinoma
• No history or concurrent seizure disorder requiring medications (e.g., antiepileptic drugs)
• No history of HIV infection, or chronic hepatitis B or C
• No active clinically serious bacterial or fungal infection (i.e., grade 2 CTCAE v. 3)
• No condition that is unstable or could jeopardize the safety of the patient and his/her compliance with the study
• No substance abuse or medical, psychological, or social condition that could interfere with adherence to the study
• No known or suspected allergy to the investigational agent or to any agent given concurrently
• No presence of asthenia or rash > CTC grade 1 at enrollment
• Must be registered in a national health-care system

PRIOR CONCURRENT THERAPY:

• No prior orthotopic liver transplantation
• Not a candidate for orthotopic liver transplantation
• No prior systemic or loco-regional treatment for HCC
• No prior organ allograft
• No treatment with any other investigational medicinal product within the past 28 days

• No concurrent treatment with full-dose anticoagulants

  • Deep-vein or catheter-associated thrombosis prophylaxis allowed
  • Warfarin or heparin therapy allowed if the coagulation parameters were within the acceptable ranges prior to initiation of anticoagulant therapy
• No concurrent or chronic co-administration of CYP3A4 inducers (e.g., rifampin, Hypericum perforatum, phenytoin, carbamazepine, phenobarbital, or dexamethasone)