Combination Chemotherapy in Patients With Zollinger-Ellison Syndrome and Tumors of the Pancreas

Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001165
Collaborator
(none)
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1
299
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Study Details

Study Description

Brief Summary

Patients with Zollinger-Ellison Syndrome suffer from ulcers of the upper gastrointestinal tract, higher than normal levels of gastric acid, and tumors of the pancreas known as non-beta islet cell tumors.

Prior to the use of drugs to cure the ulcers, patients typically died due to severe ulcers. Because of such effective drugs to treat the ulcers it is more common to see patients dying due to the pancreatic tumors.

The study will observe patients suffering from Zollinger-Ellison Syndrome and non-beta islet cell tumors and determine the effectiveness of combined chemotherapy with streptozotocin, 5-fluorouracil, and doxorubicin.

Condition or Disease Intervention/Treatment Phase
  • Drug: combined chemotherapy with streptozotocin, 5-fluorouracil, and doxorubicin
Phase 2

Detailed Description

Heretofore morbidity and risk of death in Zollinger-Ellison syndrome were caused by severe ulcer disease. The advent of specific drugs to cure ulcer disease now extends life until metastases from the non-beta-islet cell tumor cause death. The present study proposes to continue to test the effect of combined chemotherapy with streptozotocin, 5-fluorouracil and doxorubicin in biopsy-proven cases of metastatic non-beta-islet cell tumor in patients with Zollinger-Ellison syndrome. We published our initial experience with this protocol in 1988. An objective response was observed in 40% of patients.

Study Design

Study Type:
Interventional
Primary Purpose:
Treatment
Official Title:
Evaluation of Chemotherapy With Streptozotocin Combined With 5-Fluorouracil and Adriamycin in Patients With Zollinger-Ellison Syndrome and Metastatic Non-Beta-Islet Cell Neoplasm
Study Start Date :
Sep 1, 1978
Study Completion Date :
Aug 1, 2003

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    INCLUSION CRITERIA

    Subjects selected for this study will be patients with Zollinger-Ellison syndrome who are being evaluated under the protocol entitled "Diagnostic Evaluation of Patients with Suspected Abnormalities of Gastric Secretion" (80-DK-0123).

    Histologically proven gastrinoma;

    Evidence of metastatic disease or locally invasive tumor by angiography, ultrasound, computerized axial tomography, MRI scan or bone scan;

    Progression of the tumor during the preceding 6 months.

    EXCLUSION CRITERIA

    The following pre-existing conditions will exclude patients from the study:

    Congestive heart failure;

    Proteinuria greater than 1 gram/day;

    Serum creatinine greater than 1.5 mg%;

    Platelet count less than 100,000/mm3;

    White blood count less than 2500/mm3;

    Pregnancy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00001165
    Other Study ID Numbers:
    • 780133
    • 78-DK-0133
    First Posted:
    Nov 4, 1999
    Last Update Posted:
    Mar 4, 2008
    Last Verified:
    Aug 1, 2003

    Study Results

    No Results Posted as of Mar 4, 2008