Ex-Vivo Depletion of Myeloma Cells From Peripheral Blood Progenitor Cell Grafts
Primary Purpose
Multiple Myeloma
Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Apheresis
Stem Cell Transplantation
Melphalan
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Myeloma focused on measuring Myeloma, Ex-Vivo Depletion of Myeloma Cells, Peripheral Blood Progenitor Cell Grafts, PBPC, Stem Cell Transplant, Bone marrow stem cells, Melphalan, Alkeran, Apheresis
Eligibility Criteria
Inclusion Criteria:
- Patients with multiple myeloma who have relapsed after an autologous transplant or with a chemosensitive relapse more than one year post initial therapy
- Age 18 to 75 years
- Left ventricular ejection fraction >/= 40%. No uncontrolled arrhythmias
- FEV1, FVC and DLCO >/= 40%. No symptomatic pulmonary disease
- Serum bilirubin </= 2 x upper limit of normal, SGPT </= 4 x upper limit of normal
- HIV-negative
- Negative Beta HCG test in a woman with child bearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization
- Patient or guardian able to sign informed consent
- Marrow-MSC Donor Requirements: patients must have a family member who is matched at 2, 3, or 4 HLA antigens and willing to donate 80-100 ml or bone marrow for MSC generation
Exclusion Criteria:
- International Staging System (ISS) stage I at diagnosis (beta-2 microglobulin < 3.5 mg/L and albumin >/= 3.5 g/dL)
- Patients with an apheresis collection </= 7 x 10e6 CD34+/Kg
- A fully matched related donor
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Stem Cell Collection + Transplantation
Arm Description
Apheresis: On Day 5, 3 hour process to separate blood (stem cells from other cells) done 1 time a day for 1-6 days, or until enough stem cells are collected. Stem cells are cultured with donated stem cells from a relative for two weeks before being returned via transplantation. Co-culture Stem Cell Infusion on Day 0. Melphalan 100 mg/m^2 IV over 30 minutes daily on Days -2 and -1.
Outcomes
Primary Outcome Measures
Neutrophil Engraftment Rate
Secondary Outcome Measures
Full Information
NCT ID
NCT00968396
First Posted
August 27, 2009
Last Updated
April 4, 2013
Sponsor
M.D. Anderson Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT00968396
Brief Title
Ex-Vivo Depletion of Myeloma Cells From Peripheral Blood Progenitor Cell Grafts
Official Title
Ex-Vivo Depletion of Myeloma Cells From Peripheral Blood Progenitor Cell Grafts
Study Type
Interventional
2. Study Status
Record Verification Date
April 2013
Overall Recruitment Status
Withdrawn
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this clinical research study is to learn if cleaning the stem cells of a patient who has multiple myeloma (MM) with the bone marrow of a relative will make a cell product capable of replacing the bone marrow after standard treatment with chemotherapy.
Detailed Description
A transplant of one's own bone marrow stem cells is part of a standard treatment for MM. Because MM comes from the bone marrow, stem-cell products from the bone marrow can have tumor cells mixed in them when they are transplanted. This may cause the disease to return after transplant. This study will learn about a method of cleaning, or "purging," the MM tumor cells from the stem cells by using the bone marrow of a relative.
Study Drugs:
Melphalan is designed to damage the DNA (the genetic material) of cells, which may cause cancer cells to die.
Study Drug Administration:
If you are found to be eligible to take part in this study, you will be given G-CSF twice a day through a needle under the skin on Days 1-5 to move stem cells from out of the bone marrow and into the blood.
You will receive melphalan through a needle in your vein over 30 minutes each time on the 2 days directly before you receive the stem cell transplant.
Stem Cell Collection, Purging, and Transplantation:
On Day 5, stem cell collection will begin. You will have a central venous catheter (CVC - a sterile, flexible tube) placed into a vein in your chest while you are under local anesthesia. Your doctor will explain this procedure to you in more detail, and you will be required to sign a separate consent form for this procedure.
Blood will be removed from your body through the CVC and passed through a machine that separates stem cells from the other cells. The stem cells will be frozen for storage, and the blood will be returned to your body. This 3-hour process is called apheresis. This process will be done 1 time a day for 1-6 days, or until enough stem cells are collected.
Your stem cells will be placed in a sterile container, where they will grow and multiply with donated stem cells from a relative. If there are enough cells after 2 weeks, the cells will be transplanted back into the body. If there are not enough cells after the 2 weeks of growing with the donor's stem cells, they will be combined with a sample that was set aside at your initial collection and then transplanted back into the body.
Study Visits:
One (1), 2, and 6 months after the transplant, blood (about 2 teaspoons) will be drawn for routine tests and to check the status of the disease.
Six (6) months after the transplant, you will also have a bone marrow aspirate/biopsy to check the status of the disease.
Length of Study:
You will remain on study until 12 months after the transplant. You will be taken off study if the disease gets worse or needs further treatment.
End-of-Treatment Visit:
Twelve (12) months after the transplant, you will have your end-of-treatment visit. At this time, the following tests and procedures will be performed:
Blood (about 2 teaspoons) will be drawn for routine tests and to check the status of the disease.
You will have a bone marrow aspirate/biopsy.
You will have x-rays taken of your bones.
This is an investigational study. Melphalan is FDA approved and commercially available for the treatment of MM. While receiving a stem-cell transplant is standard treatment for MM, cleaning (purging) the stem-cell product is investigational.
Up to 25 recipients will take part in this study. All will be enrolled at M. D. Anderson
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
Myeloma, Ex-Vivo Depletion of Myeloma Cells, Peripheral Blood Progenitor Cell Grafts, PBPC, Stem Cell Transplant, Bone marrow stem cells, Melphalan, Alkeran, Apheresis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Stem Cell Collection + Transplantation
Arm Type
Experimental
Arm Description
Apheresis: On Day 5, 3 hour process to separate blood (stem cells from other cells) done 1 time a day for 1-6 days, or until enough stem cells are collected. Stem cells are cultured with donated stem cells from a relative for two weeks before being returned via transplantation. Co-culture Stem Cell Infusion on Day 0. Melphalan 100 mg/m^2 IV over 30 minutes daily on Days -2 and -1.
Intervention Type
Procedure
Intervention Name(s)
Apheresis
Intervention Description
On Day 5, 3 hour process to separate blood (stem cells from other cells) done 1 time a day for 1-6 days, or until enough stem cells are collected. Stem cells are cultured with donated stem cells from a relative for two weeks before being returned via transplantation.
Intervention Type
Procedure
Intervention Name(s)
Stem Cell Transplantation
Intervention Description
Co-culture Stem Cell Infusion on Day 0.
Intervention Type
Drug
Intervention Name(s)
Melphalan
Other Intervention Name(s)
Alkeran
Intervention Description
100 mg/m^2 IV over 30 minutes daily on Days -2 and -1
Primary Outcome Measure Information:
Title
Neutrophil Engraftment Rate
Time Frame
28 Days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with multiple myeloma who have relapsed after an autologous transplant or with a chemosensitive relapse more than one year post initial therapy
Age 18 to 75 years
Left ventricular ejection fraction >/= 40%. No uncontrolled arrhythmias
FEV1, FVC and DLCO >/= 40%. No symptomatic pulmonary disease
Serum bilirubin </= 2 x upper limit of normal, SGPT </= 4 x upper limit of normal
HIV-negative
Negative Beta HCG test in a woman with child bearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization
Patient or guardian able to sign informed consent
Marrow-MSC Donor Requirements: patients must have a family member who is matched at 2, 3, or 4 HLA antigens and willing to donate 80-100 ml or bone marrow for MSC generation
Exclusion Criteria:
International Staging System (ISS) stage I at diagnosis (beta-2 microglobulin < 3.5 mg/L and albumin >/= 3.5 g/dL)
Patients with an apheresis collection </= 7 x 10e6 CD34+/Kg
A fully matched related donor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yago Nieto, MD, PHD
Organizational Affiliation
UT MD Anderson Cancer Center
Official's Role
Study Chair
12. IPD Sharing Statement
Links:
URL
http://www.mdanderson.org
Description
UT MD Anderson Cancer Center website
Learn more about this trial
Ex-Vivo Depletion of Myeloma Cells From Peripheral Blood Progenitor Cell Grafts
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