Clinical Trials Directory

Trials / Completed

CompletedNCT00006232

Combination Chemotherapy in Treating Patients With Stage II or Stage III Multiple Myeloma

A Randomized Trial Comparing Z-Dex With VAD as Induction Therapy for Patients With Multiple Myeloma

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
West of Scotland Lymphoma Group · Academic / Other
Sex
All
Age
75 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. It is not yet known which combination chemotherapy regimen is more effective for multiple myeloma. PURPOSE: This randomized phase III trial is comparing two combination chemotherapy regimens to see how well they work in treating patients with stage II or stage III multiple myeloma.

Detailed description

OBJECTIVES: * Compare the partial and complete response rates in patients with multiple myeloma treated with induction therapy comprising idarubicin and dexamethasone vs vincristine, doxorubicin, and dexamethasone. * Compare the disease progression, time to achieve maximal response, and duration of response in patients treated with these 2 regimens. * Compare the quality of life of patients treated with these 2 regimens. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral idarubicin and oral dexamethasone daily on days 1-4. Treatment continues every 3 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients also receive oral dexamethasone daily on days 8-11 during course 1 only. * Arm II: Patients receive oral dexamethasone daily, doxorubicin IV continuously, and vincristine IV continuously on days 1-4. Courses repeat as in arm I. Patients receive additional dexamethasone as in arm I. Patients without a maximal response after completion of course 4 may receive up to 2 additional courses. Quality of life is assessed at baseline and then prior to each study course. Patients are followed for survival. PROJECTED ACCRUAL: A total of 200 patients (100 per arm) will be accrued for this study within 2 years.

Conditions

Interventions

TypeNameDescription
DRUGdexamethasone
DRUGdoxorubicin hydrochloride
DRUGidarubicin
DRUGvincristine sulfate

Timeline

Start date
1996-10-01
Completion
2007-08-01
First posted
2003-01-27
Last updated
2013-05-15

Locations

12 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00006232. Inclusion in this directory is not an endorsement.