Autologous Transplantation for Multiple Myeloma
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Purpose
The present study was designed in an attempt to prospectively evaluate in a randomized fashion whether further cytotoxic dose intensification, as delivered with two sequential autologous stem-cell transplantations, improved the outcome of younger patients with newly diagnosed multiple myeloma in comparison with a single autologous transplantation.
| Condition | Intervention | Phase |
|---|---|---|
|
Multiple Myeloma |
Procedure: Autologous Stem Cell Transplantation |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Prospective, Randomized Study of Single Versus Double Autologous Stem Cell Transplantation for Multiple Myeloma |
- Complete or near Complete Response Rate
- Relapse-free Survival
- Event-free Survival
- Overall Survival
| Estimated Enrollment: | 324 |
| Study Start Date: | January 1996 |
| Estimated Study Completion Date: | November 2005 |
Following demonstration that single autologous transplantation for the treatment of younger patients with newly diagnosed multiple myeloma prolonged overall survival in comparison with conventional chemotherapy, double autologous transplantation was tested, initially in refractory myeloma and subsequently to include also patients with newly diagnosed disease. To explore the role of double autologous stem-cell transplantation as part of up-front therapy for multiple myeloma, in 1996 we launched a prospective, randomized trial comparing a single course of stem-cell-supported melphalan with the same regimen followed, after three to six months, by a second autologous transplantation in support of melphalan and busulfan. The study was designed to detect a 15 percent increase in complete or near complete response rate with double transplants compared to a single transplantation. With a 2-sided significance level α = 0.05 and a power 1-β = 0.80, 162 patients were required in each treatment arm of the study to detect a statistically significant increase in complete or near complete response rate from 30% in the single-transplant arm to 45% in the double-transplant arm. Primary study endpoint was the complete or near complete response rate. Secondary study endpoints were relapse-free survival, event-free survival and overall survival. The recruitment target was 324 patients.
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Previously untreated
- Younger than 61 years
- Symptomatic myeloma
- Measurable disease
- Fit to receive high-dose chemotherapy
Exclusion Criteria:
- M-GUS
- Solitary plasmacytoma
- Plasma cell leukemia
- AL Amyloidosis
Contacts and Locations
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00378222 History of Changes |
| Other Study ID Numbers: | BO96 |
| Study First Received: | September 18, 2006 |
| Last Updated: | September 18, 2006 |
| Health Authority: | Italy: Ministry of Health |
Keywords provided by University of Bologna:
|
Myeloma previously untreated Single autologous transplantation Double autologous transplantation Complete response |
Additional relevant MeSH terms:
|
Multiple Myeloma Neoplasms, Plasma Cell Neoplasms by Histologic Type Neoplasms Hemostatic Disorders Vascular Diseases Cardiovascular Diseases |
Paraproteinemias Blood Protein Disorders Hematologic Diseases Hemorrhagic Disorders Lymphoproliferative Disorders Immunoproliferative Disorders Immune System Diseases |
ClinicalTrials.gov processed this record on May 23, 2013