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

No results posted yet for this study

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

cyclophosphamide

650 mg/m\^2

DRUG

cytarabine

300 mg/m\^2

DRUG

doxorubicin hydrochloride

25 mg/m\^2

DRUG

etoposide

120 mg/m\^2

DRUG

methotrexate

120 mg/m\^2

DRUG

prednisone

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00002657 on ClinicalTrials.gov