Radiation Therapy Plus Chemotherapy in Treating Patients With Pancreatic Cancer
Study Details
Study Description
Brief Summary
RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy combined with chemotherapy may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of brachytherapy followed by external-beam radiation therapy plus chemotherapy in treating patients who have pancreatic cancer that cannot be removed surgically.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
OBJECTIVES:
- Determine the response/remission rate, survival, and degree of local control from interstitial colloidal phosphorus P32 followed by external beam radiotherapy and chemotherapy in patients with unresectable pancreatic cancer.
OUTLINE: Patients are stratified according to prior therapy (yes vs no).
Patients receive dexamethasone intratumorally, then macroaggregated albumin and interstitial phosphorus P32 intratumorally. Most patients receive a second course of this brachytherapy.
Patients then proceed to chemoradiotherapy beginning 7-14 days after brachytherapy. Radiotherapy is administered 5 days a week for 6.4 weeks. Fluorouracil IV is administered every other day for 4 doses during weeks 1 and 2.
Patients are followed monthly for 1 year then every 3 months thereafter.
PROJECTED ACCRUAL: A total of 48 patients will be accrued for this study.
Study Design
Outcome Measures
Primary Outcome Measures
- Response rate []
- Duration of remission []
- Survival []
Secondary Outcome Measures
- Patterns of failure []
Eligibility Criteria
Criteria
DISEASE CHARACTERISTICS:
-
Histologically proven unresectable adenocarcinoma of the pancreas limited to the head, body, or tail of the pancreas
-
Diameter no greater than 5 cm
-
Volume no greater than 66 mL
-
No ascites (with or without tumor cells)
-
No endoscopically proven tumor penetration of duodenum or stomach
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- Karnofsky 70-100%
Hematopoietic:
-
WBC at least 3,000/mm3
-
Platelet count at least 100,000/mm3
-
Hemoglobin at least 9 g/dL (transfusion allowed)
Hepatic:
-
No hepatic disease
-
At least 50% uptake of technetium-sulfur colloid in normal liver if cirrhosis suspected
-
No vascular occlusion of portal system
Renal:
-
Creatinine no greater than 1.5 mg/dL
-
BUN no greater than 25 mg/dL
Other:
-
No Crohn's disease, ulcerative colitis, or other inflammatory bowel disease
-
Not pregnant
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- If prior chemotherapy, test dose of colloidal phosphorous P32 administered prior to attempted treatment
Endocrine therapy:
- Not specified
Radiotherapy:
- No prior radiotherapy to pancreas, liver, or upper gastrointestinal tract
Surgery:
-
No complete surgical resection
-
No splenectomy
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Northside Hospital Cancer Center | Atlanta | Georgia | United States | 30342-1611 |
| 2 | Center for Molecular Medicine | Garden City | New York | United States | 11530 |
Sponsors and Collaborators
- Center for Molecular Medicine
Investigators
- Study Chair: Stanley E. Order, MD, ScD, FACR, Center for Molecular Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CMM-95079
- CDR0000064415
- CH/UMC-95079
- NCI-V95-0760