Status:
COMPLETED
A Randomized Trial to Compare Busulfan + Melphalan 140 mg/m2 With Melphalan 200 mg/m2 as Preparative Regimen for Autologous Hematopoietic Stem Cell Transplantation for Multiple Myeloma
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborating Sponsors:
Otsuka Pharmaceutical Development & Commercialization, Inc.
Conditions:
Myeloma
Eligibility:
All Genders
18-70 years
Phase:
PHASE3
Brief Summary
The goal of this clinical research study is to compare Busulfex (busulfan) with or without Alkeran (melphalan) to learn which study therapy may be better at helping to control MM in patients who will ...
Detailed Description
Study Groups: If you are found to be eligible to take part in this study, you will be randomly assigned (as in the flip of a coin) to 1 of 2 study groups. * Group 1 will receive melphalan and busulf...
Eligibility Criteria
Inclusion
- Patients with multiple myeloma in complete remission (CR), partial remission (PR), or very good partial remission (VGPR), or symptomatic stable disease (no evidence of progression) including patients with light chain MM detected in the serum by free light chain assay.
- Patients with non-secretory multiple myeloma \[absence of a monoclonal protein (M protein) in serum as measured by electrophoresis (SPEP) and immunofixation (SIFE) and the absence of Bence Jones protein in the urine (UPEP) defined by use of conventional electrophoresis and immunofixation (UIFE) techniques\] but with measurable disease on imaging studies like MRI, CT scan or PET scan.
- Who have received at least two cycles of initial systemic therapy and are within 2 to 12 months of the first dose. Mobilization therapy is not considered initial therapy.
- 70 years of age or younger.
- Karnofsky performance score 70% or higher.
- Cardiac function: left ventricular ejection fraction at rest \> 40% within 3 months of registration.
- Hepatic function: bilirubin \< 2x the upper limit of normal and ALT and AST \< 2.5x the upper limit of normal.
- Renal function: creatinine clearance of \>/= 40 mL/min, estimated or calculated.
- Pulmonary function: DLCO, FEV1, FVC \>/= 50% of predicted value (corrected for hemoglobin) within 3 months of registration
- Signed informed consent form.
Exclusion
- Patients with uncontrolled bacterial, viral or fungal infections (currently taking medication and progression of clinical symptoms).
- Patients seropositive for the human immunodeficiency virus (HIV).
- Patients with history of myocardial infarction within 6 months prior to enrollment or has New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities.
- Patients participating in an investigational new drug protocol within 14 days before enrollment.
- Female patients who are pregnant (positive b-HCG) or breastfeeding.
- Prior stem cell transplantation allogeneic or autologous.
- Prior organ transplant requiring immunosuppressive therapy.
Key Trial Info
Start Date :
September 30 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 10 2019
Estimated Enrollment :
205 Patients enrolled
Trial Details
Trial ID
NCT01413178
Start Date
September 30 2011
End Date
March 10 2019
Last Update
April 21 2020
Active Locations (1)
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1
University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030