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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Withdrawn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
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with multiple myeloma who have relapsed after an autologous transplant or with a chemosensitive relapse more than one year post initial therapy
  2. Age 18 to 75 years
  3. Left ventricular ejection fraction >/= 40%. No uncontrolled arrhythmias
  4. FEV1, FVC and DLCO >/= 40%. No symptomatic pulmonary disease
  5. Serum bilirubin </= 2 x upper limit of normal, SGPT </= 4 x upper limit of normal
  6. HIV-negative
  7. Negative Beta HCG test in a woman with child bearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization
  8. Patient or guardian able to sign informed consent
  9. 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:

  1. International Staging System (ISS) stage I at diagnosis (beta-2 microglobulin < 3.5 mg/L and albumin >/= 3.5 g/dL)
  2. Patients with an apheresis collection </= 7 x 10e6 CD34+/Kg
  3. 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

    First Posted
    August 27, 2009
    Last Updated
    April 4, 2013
    Sponsor
    M.D. Anderson Cancer Center
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    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

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    Ex-Vivo Depletion of Myeloma Cells From Peripheral Blood Progenitor Cell Grafts

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