Antineoplaston Therapy in Treating Patients With Advanced Head and Neck Cancer
Sponsored by Burzynski Research Institute
About this trial
Last updated 8 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 27 years ago
What is this trial about?
What are the Participation Requirements?
DISEASE CHARACTERISTICS:
- Histologically confirmed cancer of the head and neck that is unlikely to respond to
existing therapy and for which no curative therapy exists
- Metastatic disease OR incurable with surgery or radiation
- Measurable disease by CT scan or MRI
- Tumor must be at least 2 cm for the lymph nodes located in the head, neck,
axillary, inguinal or femoral areas and at least 0.5 cm for other areas
PATIENT CHARACTERISTICS:
Age:
- 16 and over
Performance status:
- Karnofsky 60-100%
Life expectancy:
- At least 2 months
Hematopoietic:
- WBC at least 2,000/mm^3
- Platelet count at least 50,000/mm^3
Hepatic:
- No hepatic insufficiency
- Bilirubin no greater than 2.5 mg/dL
- SGOT and SGPT no greater than 2.5 mg/dL
Renal:
- No renal insufficiency
- Creatinine no greater than 2.5 mg/dL
- No renal conditions that contraindicate high dosages of sodium
Cardiovascular:
- No chronic heart failure
- No uncontrolled hypertension
- No history of congestive heart failure
- No other cardiovascular conditions that contraindicate high dosages of sodium
Pulmonary:
- No serious lung disease (e.g., severe chronic obstructive pulmonary disease)
Other:
- Not pregnant or nursing
- Fertile patients must use effective contraception during and for 4 weeks after study
participation
- No other serious medical or psychiatric conditions
- No active infection
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- At least 4 weeks since prior immunotherapy and recovered
- No concurrent immunomodulatory agents
Chemotherapy:
- At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas) and recovered
- No concurrent antineoplastic therapy
Endocrine therapy:
- Concurrent corticosteroids allowed
Radiotherapy:
- See Disease Characteristics
- At least 8 weeks since prior radiotherapy (unless multiple tumors) and recovered
Surgery:
- See Disease Characteristics
Other:
- Prior cytodifferentiating agents allowed