SWOG-9239 Reduction of Immunosuppression Plus Interferon Alfa and Combination Chemotherapy in Treating Patients With Malignant Tumors That Develop After Organ Transplant
NCT00002657 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2013-01-24
Summary
RATIONALE: Reducing the amount of drugs used to prevent transplant rejection may help a person's body kill tumor cells. Giving biological therapy, such as interferon alfa, which may interfere with the growth of cancer cells, or combination chemotherapy, which uses different ways to stop tumor cells from dividing so they stop growing or die, may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of reducing immunosuppression, and giving interferon alfa and combination chemotherapy, in treating patients who have malignant tumors that develop after organ transplant.
Conditions
- Lymphoma
- Multiple Myeloma and Plasma Cell Neoplasm
Interventions
- BIOLOGICAL
-
bleomycin sulfate
5 mg/m\^2
- BIOLOGICAL
-
recombinant interferon alfa
3.0 x 10\^6 IU/m\^2
- DRUG
-
650 mg/m\^2
- DRUG
-
300 mg/m\^2
- DRUG
-
doxorubicin hydrochloride
25 mg/m\^2
- DRUG
-
etoposide
120 mg/m\^2
- DRUG
-
methotrexate
120 mg/m\^2
- DRUG
-
dose varies during initial immunosuppression. During chemotherapy, 60 mg/m\^2.
- DRUG
-
vincristine sulfate
1.4 mg/m\^2
- PROCEDURE
-
conventional surgery
Simple excision, for those patients who have resectable disease after initial immunosuppression.
- RADIATION
-
radiation therapy
For treatment of localized disease that remains after initial immunosuppression.
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Eastern Cooperative Oncology Group
collaborator NETWORK -
SWOG Cancer Research Network
lead NETWORK
Principal Investigators
-
Lode J. Swinnen, MD · Loyola University
-
Leo I. Gordon, MD · Robert H. Lurie Cancer Center
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 15 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1995-05-31
- Primary Completion
- 2003-11-30
- Completion
- 2011-07-31
Countries
- United States
Study Locations
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