Overview

Bevacizumab and Chemoembolization in Treating Patients With Liver Cancer That Cannot Be Removed By Surgery

Status:
Completed
Trial end date:
2011-02-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Chemoembolization kills tumor cells by carrying chemotherapy drugs directly into the tumor and blocking the blood flow to the tumor. Giving bevacizumab together with chemoembolization may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving bevacizumab together with chemoembolization works in treating patients with liver cancer that cannot be removed by surgery.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sidney Kimmel Comprehensive Cancer Center
Yale University
Collaborators:
National Cancer Institute (NCI)
Northwestern University
Treatments:
Bevacizumab
Criteria
DISEASE CHARACTERISTICS:

- Histologically confirmed* hepatocellular carcinoma

- Unresectable disease

- Child's class A or B with liver-predominant and asymptomatic extrahepatic disease
NOTE: *A highly suspicious liver mass on CT scan or MRI in the presence of alpha
fetoprotein > 200 mg/dL may be used as alternative diagnostic criterion

PATIENT CHARACTERISTICS:

- Eastern Cooperative Oncology Group (ECOG) performance status 0-2

- Absolute neutrophil count > 1,500/mm³

- Platelet count > 50,000/mm³

- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5.0 times upper
limit of normal (ULN)

- Bilirubin ≤ 5.0 mg/dL

- Creatinine normal OR creatinine clearance > 50 mL/min

- No significant traumatic injury within the past 28 days

- No abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within
the past 6 months

- No serious, nonhealing wound, ulcer, or bone fracture

PRIOR CONCURRENT THERAPY:

- No major surgery or open biopsy within the past 28 days

- No minor surgery (e.g., fine-needle aspirations or core biopsies) within the past 7
days

- No chemotherapy within the past 4 weeks

- No radiotherapy within the past 21 days

- No concurrent major surgery

- No other concurrent chemotherapy

- No other concurrent investigational drugs