Overview

Chemotherapy Compared to Biological Therapy in Treating Patients With Cancer of the Pancreas

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Biological therapies use different ways to stimulate the immune system and stop cancer cells from growing. It is not yet known whether chemotherapy is more effective than biological therapy in treating patients with cancer of the pancreas. PURPOSE: Randomized phase II trial to compare the effectiveness of gemcitabine with biological therapy in treating patients who have cancer of the pancreas that cannot be surgically removed.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Meyer Pharmaceuticals
Treatments:
Gemcitabine
Criteria
DISEASE CHARACTERISTICS: Histologically proven stage II, III, or IV pancreatic cancer that
is unresectable No symptomatic third space fluid collection (e.g., ascites, pleural
effusion)

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Karnofsky 70-100% Life
expectancy: At least 3 months Hematopoietic: WBC at least 3,500/mm3 Platelet count at least
100,000/mm3 Hematocrit at least 33% Hemoglobin at least 10.5 g/dL Hepatic: Bilirubin no
greater than 3.0 mg/dL SGOT or SGPT no greater than 3 times upper limit of normal Renal:
Creatinine no greater than 1.5 mg/dL Cardiovascular: No history of myocardial infarction
within past 3 months No congestive heart failure Other: HIV negative No other prior
malignancy except basal cell skin cancer No persistent fever greater than 102 degrees F (39
degrees C) unless caused by the pancreatic cancer Not pregnant or nursing Fertile patients
must use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy: No prior biologic therapy (e.g., interferons,
interleukins) Chemotherapy: No prior chemotherapy Endocrine therapy: No concurrent systemic
steroids Radiotherapy: No prior radiotherapy Surgery: At least 30 days since prior surgery
Decompressive surgery and endoscopic stenting (including expandable wire stents) allowed to
relieve symptoms of disease Other: At least 30 days since prior investigational therapy
Palliative care to relieve symptoms of disease allowed, including pain management and
celiac block by endoscopic ultrasonography or percutaneously