Liver Cancer
Conditions
Keywords
adult primary hepatocellular carcinoma, advanced adult primary liver cancer, localized resectable adult primary liver cancer, localized unresectable adult primary liver cancer
Brief summary
RATIONALE: Vaccines made from DNA and a gene-modified virus may make the body build an immune response to kill tumor cells. Giving booster vaccinations may make a stronger immune response and prevent or delay the recurrence of liver cancer. PURPOSE: This phase I/II trial is studying the side effects and best dose of vaccine therapy and to see how well it works in treating patients with stage II, stage IIIA, stage IIIB, or stage IVA liver cancer.
Detailed description
OBJECTIVES: Primary * Determine the dose-limiting toxicity and maximum tolerated dose of adjuvant vaccination comprising alpha fetoprotein (AFP) plasmid DNA and sargramostim (GM-CSF) plasmid DNA followed by AFP adenoviral vector boost in patients with HLA-A\*0201-expressing stage II-IVA hepatocellular carcinoma. Secondary * Determine the optimal biological dose of this regimen, as defined by the generation of AFP-specific immunity, in these patients. * Determine disease-free survival of patients treated with this regimen. OUTLINE: This is a dose-escalation study of alpha fetoprotein (AFP) adenoviral vector boost. Patients receive vaccination comprising AFP plasmid DNA and sargramostim (GM-CSF) plasmid DNA intramuscularly (IM) on days 1, 30, and 60 in the absence of unacceptable toxicity. Patients then receive boost immunization comprising AFP adenoviral vector IM and intradermally on day 90. Cohorts of 3-6 patients receive escalating doses of AFP adenoviral vector boost until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Patients are followed monthly for 3 months and then every 6 months thereafter. PROJECTED ACCRUAL: A total of 3-25 patients will be accrued for this study.
Interventions
BIOLOGICALalpha fetoprotein adenoviral vector vaccine
BIOLOGICALalpha fetoprotein plasmid DNA vaccine
BIOLOGICALsargramostim plasmid DNA hepatocellular carcinoma vaccine adjuvant
Sponsors
National Cancer Institute (NCI)
Jonsson Comprehensive Cancer Center
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Diagnosis of hepatocellular carcinoma * Stage II-IVA disease * No active disease after local or regional therapy (e.g., surgical resection, radiofrequency ablation, cryoablation, or ethanol injection) * Serum alpha fetoprotein \> upper limit of normal * HLA-A\*0201 positive by DNA subtyping PATIENT CHARACTERISTICS: Age * Over 18 Performance status * Karnofsky 70-100% Life expectancy * Not specified Hematopoietic * Hemoglobin \> 9.0 g/dL (transfusion independent) * Platelet count \> 50,000/mm\^3 * Absolute neutrophil count \> 1,000/mm\^3 Hepatic * Child Pugh class A or B liver function * Hepatitis B or C viral infection allowed Renal * Not specified Cardiovascular * No New York Heart Association class III or IV cardiac insufficiency * No coronary artery disease Immunologic * HIV negative * No other acute viral, bacterial, or fungal infection requiring therapy * No allergy to study agents * No history of opportunistic infection * No high serum titer of neutralizing anti-adenoviral antibodies * No congenital or acquired condition resulting in an inability to generate an immune response Other * Not pregnant * Negative pregnancy test * Fertile patients must use effective double-method (including a barrier method) contraception * No other condition that would preclude study participation PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * At least 30 days since prior chemotherapy * No concurrent cytotoxic chemotherapy Endocrine therapy * At least 30 days since prior steroid therapy * No concurrent steroid therapy, including corticosteroids Radiotherapy * Not specified Surgery * See Disease Characteristics * No prior organ allograft Other * At least 2 weeks since prior therapy for acute infection * No concurrent immunosuppressive therapy * No concurrent cyclosporine
Outcome results
None listed