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| Sponsor: | Eastern Cooperative Oncology Group |
|---|---|
| Collaborator: |
National Cancer Institute (NCI) |
| Information provided by: | National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: | NCT00002556 |
Purpose
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Interferon alfa may interfere with the growth of cancer cells. It is not yet known whether combination chemotherapy plus interferon alfa is more effective than combination chemotherapy alone in treating patients with multiple myeloma.
PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy with or without interferon alfa in treating patients who have previously untreated stage I, stage II, or stage III multiple myeloma.
| Condition | Intervention | Phase |
|---|---|---|
|
Multiple Myeloma and Plasma Cell Neoplasm |
Biological: filgrastim Biological: recombinant interferon alfa Drug: carmustine Drug: cyclophosphamide Drug: melphalan Drug: prednisone Drug: vincristine sulfate |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Primary Purpose: Treatment |
| Official Title: | THE TREATMENT OF MULTIPLE MYELOMA UTILIZING VBMCP CHEMOTHERAPY ALTERNATING WITH HIGH-DOSE CYCLOPHOSPHAMIDE AND ALPHA 2B-INTERFERON VERSUS VBMCP: A PHASE III STUDY FOR PREVIOUSLY UNTREATED MULTIPLE MYELOMA |
| Estimated Enrollment: | 289 |
| Study Start Date: | April 1994 |
| Primary Completion Date: | May 2009 (Final data collection date for primary outcome measure) |
OBJECTIVES:
OUTLINE: This is a randomized study. Patients are stratified according to creatinine (less than 2.0 vs 2.0 mg/dL or greater), performance status (0-1 vs 2-4), plasma cell labeling index (2% or more vs less than 2% vs approved unknown/not interpretable), and beta-2 microglobulin (4 micrograms/dL or greater vs less than 4 micrograms/dL vs approved unknown/not interpretable).
Consolidation: Patients are then randomized to 1 of 2 treatment arms.
After documentation of plateau, patients receive 2 additional courses of VBMCP (arm I) or 2 additional courses of VBMCP alternating with 2 courses of IFN-A (arm II) in the absence of disease progression. Treatment for arms I and II continues for 1-2 years in the absence of a plateau state plus 2 additional courses of VBMCP (arm I) or 2 courses each of VBMCP and IFN-A (arm II); disease progression; or unacceptable toxicity. Patients undergo observation beginning after completion of the 2 post-plateau courses and continuing in the absence of disease progression. Patients with disease progression after 3 months on observation receive reinduction comprising the consolidation regimen to which they were originally randomized. Reinduction continues in the absence of disease progression.
Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.
PROJECTED ACCRUAL: A total of 289 patients will be accrued for this study within approximately 8 years.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Diagnosis of previously untreated, stage I-III multiple myeloma confirmed by:
At least 1 of the following:
Measurable disease
PATIENT CHARACTERISTICS:
Age:
Performance status:
Life expectancy:
Hematopoietic:
Hepatic:
Renal:
Cardiovascular:
No significant arrhythmia within the past 3 months, i.e.:
Pulmonary:
Other:
PRIOR CONCURRENT THERAPY:
Biologic therapy:
Chemotherapy:
Endocrine therapy:
Radiotherapy:
Surgery:
Other:
Contacts and Locations| United States, Illinois | |
| CCOP - Illinois Oncology Research Association | |
| Peoria, Illinois, United States, 61602 | |
| United States, Wisconsin | |
| CCOP - St. Vincent Hospital Cancer Center, Green Bay | |
| Green Bay, Wisconsin, United States, 54301 | |
| Study Chair: | Robert A. Kyle, MD | Mayo Clinic |
More Information
| ClinicalTrials.gov Identifier: | NCT00002556 History of Changes |
| Other Study ID Numbers: | CDR0000063435, E-5A93 |
| Study First Received: | November 1, 1999 |
| Last Updated: | May 29, 2009 |
| Health Authority: | United States: Federal Government |
|
stage I multiple myeloma stage II multiple myeloma stage III multiple myeloma |
|
Neoplasms Multiple Myeloma Neoplasms, Plasma Cell Plasmacytoma Neoplasms by Histologic Type Hemostatic Disorders Vascular Diseases Cardiovascular Diseases Paraproteinemias Blood Protein Disorders Hematologic Diseases Hemorrhagic Disorders Lymphoproliferative Disorders Immunoproliferative Disorders Immune System Diseases |
Interferon-alpha Interferon Alfa-2a Interferons Cyclophosphamide Melphalan Lenograstim Carmustine Prednisone Vincristine Antiviral Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Immunologic Factors Physiological Effects of Drugs |