Triacetyluridine and Fluorouracil Compared With Gemcitabine in Treating Patients With Unresectable Locally Advanced, or Metastatic Pancreatic Cancer
Sponsored by Wellstat Therapeutics
About this trial
Last updated 13 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Started 24 years ago
What is this trial about?
What are the Participation Requirements?
DISEASE CHARACTERISTICS:
- Histologically or cytologically confirmed adenocarcinoma of the pancreas
- Unresectable locally advanced or metastatic disease
- Stage II, III, or IV
- Measurable or evaluable disease
- No elevated tumor marker (CA 19-9) only
- No clinically significant third-space fluid accumulation (e.g., ascites or pleural
effusion)
- No carcinoid, islet cell, or lymphoma of the pancreas
- No prior or concurrent brain or leptomeningeal metastases
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- Karnofsky 70-100%
Life expectancy:
- At least 3 months
Hematopoietic:
- WBC at least 3,500/mm^3
- Platelet count at least 100,000/mm^3
- Hemoglobin at least 9.5 g/dL
Hepatic:
- Bilirubin no greater than 2.0 mg/dL
- ALT or AST less than 3 times upper limit of normal (ULN) (5 times ULN if liver
metastases present)
- No uncontrolled hepatic dysfunction
Renal:
- Creatinine less than 2.0 mg/dL
- No uncontrolled renal dysfunction
Cardiovascular:
- No uncontrolled cardiovascular disease requiring therapy, including the following:
- Angina
- Arrhythmias
- Uncompensated cardiac failure
- Myocardial infarction within the past 6 months
Pulmonary:
- No uncontrolled pulmonary dysfunction
Gastrointestinal:
- Able to take and/or retain oral medication
- No uncontrolled malabsorption syndrome or any other condition that would interfere
with intestinal absorption
Other:
- No known allergy to fluorouracil (5-FU), gemcitabine, triacetyluridine, or any of
their components
- No dihydropyrimidine-dehydrogenase deficiency
- No active uncontrolled infection
- No uncontrolled neurologic or psychiatric dysfunction
- No other malignancy except previously resected basal cell cancer or curatively
resected stage I or less cervical cancer that has been disease free for at least 5
years
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- HIV negative
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- No concurrent biologic therapy (including immunotherapy) for cancer
Chemotherapy:
- No prior chemotherapy for cancer other than as a radiosensitizer
- No prior 5-FU or gemcitabine other than as a radiosensitizer
- No prior triacetyluridine
- No other concurrent chemotherapy (including leucovorin calcium) for cancer
Endocrine therapy:
- No concurrent hormonal therapy for cancer
- Concurrent megestrol, oral contraceptives, or postmenopausal estrogen replacement
therapy allowed
Radiotherapy:
- Prior radiotherapy allowed
- No concurrent radiotherapy
Surgery:
- See Disease Characteristics
- Prior resection of pancreas allowed
Other:
- At least 30 days since prior investigational drug or therapeutic device
- No other concurrent anticancer therapy
- No other concurrent investigational drugs or devices
- No concurrent drugs that would interact adversely with 5-FU or gemcitabine