Triacetyluridine and Fluorouracil Compared With Gemcitabine in Treating Patients With Unresectable Locally Advanced, or Metastatic Pancreatic Cancer
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Purpose
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving the drugs in different combinations may kill more tumor cells. Chemoprotective drugs such as triacetyluridine may protect normal cells from the side effects of chemotherapy. It is not yet known which chemotherapy regimen is more effective in treating pancreatic cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of fluorouracil plus triacetyluridine with that of gemcitabine in treating patients who have locally advanced or metastatic pancreatic cancer that cannot be treated with surgery.
| Condition | Intervention | Phase |
|---|---|---|
|
Drug/Agent Toxicity by Tissue/Organ Pancreatic Cancer |
Drug: fluorouracil Drug: gemcitabine hydrochloride Drug: triacetyluridine |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | An Open Label, Randomized, Controlled, Phase III, Multi-center, Clinical Trial Of PN401 With High Dose 5-Fluorouracil (5FU) Versus Gemcitabine For Treatment Of Patients With Advanced Pancreatic Cancer |
- Open Label Randomized Phase 3 Multi-Center Trial of PN401 plus high dose 5-FU versus Gemcitabine in Advanced Pancreatic Cancer Patients [ Time Frame: Disease progression ] [ Designated as safety issue: No ]
| Enrollment: | 250 |
| Study Start Date: | February 2001 |
| Primary Completion Date: | February 2006 (Final data collection date for primary outcome measure) |
-
Drug: fluorouracil
OBJECTIVES:
- Compare the survival of patients with unresectable locally advanced or metastatic pancreatic cancer treated with triacetyluridine and high-dose fluorouracil vs gemcitabine.
- Compare the time to tumor progression, overall response rate, and response duration in patients treated with these regimens.
- Compare the safety of these regimens in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to disease stage (II or III vs IV). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive high-dose fluorouracil (5-FU) IV over 30 minutes once weekly on weeks 1-3 followed by 1 week of rest. After each dose of 5-FU, patients receive oral triacetyluridine every 8 hours for a total of 8 doses. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
- Arm II: Patients receive gemcitabine IV over 30 minutes once weekly on weeks 1-7 followed by 1 week of rest (course 1). Subsequent courses are given on weeks 1-3. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Patients are followed for survival.
PROJECTED ACCRUAL: A total of 260 patients (130 per treatment arm) will be accrued for this study within 30 months.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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
Contacts and Locations
Show 29 Study Locations| Study Chair: | Lenny Smith, MS | Wellstat Therapeutics |
More Information
Additional Information:
No publications provided
| Responsible Party: | Wellstat Therapeutics |
| ClinicalTrials.gov Identifier: | NCT00024427 History of Changes |
| Other Study ID Numbers: | CDR0000068931, WELLSTAT-401.00.001, PRONEURON-401.00.001, UAB-0105, UAB-F010524008 |
| Study First Received: | September 13, 2001 |
| Last Updated: | June 27, 2012 |
| Health Authority: | United States: Federal Government United States: Food and Drug Administration |
Keywords provided by Wellstat Therapeutics:
|
drug/agent toxicity by tissue/organ stage II pancreatic cancer stage III pancreatic cancer |
recurrent pancreatic cancer adenocarcinoma of the pancreas stage IV pancreatic cancer |
Additional relevant MeSH terms:
|
Pancreatic Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms Endocrine Gland Neoplasms Digestive System Diseases Pancreatic Diseases Endocrine System Diseases Fluorouracil Gemcitabine Antimetabolites Molecular Mechanisms of Pharmacological Action |
Pharmacologic Actions Antimetabolites, Antineoplastic Antineoplastic Agents Therapeutic Uses Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Antiviral Agents Anti-Infective Agents Enzyme Inhibitors Radiation-Sensitizing Agents |
ClinicalTrials.gov processed this record on May 22, 2013