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Autologous Bone Marrow Transplantation (BMT) Compared With Allogeneic BMT in Multiple Myeloma

Primary Purpose

Multiple Myeloma

Status
Unknown status
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Autologous bone marrow transplantation
Allogeneic bone marrow transplantation
Sponsored by
Tehran University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma focused on measuring MM

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age at diagnosis equal or under 55 year
  • Meeting the Durie and Salmon criteria for initial diagnosis of MM
  • Stage II or III MM at diagnosis or anytime thereafter
  • Symptomatic MM requiring treatment at diagnosis or anytime thereafter
  • If receiving chemotherapy-based mobilization regimens, must be able to receive high-dose melphalan between 2 and 8 weeks after the initiation of mobilization therapy whether delivered at the transplant center or at a referring center
  • Adequate organ function as measured by:

    • Cardiac: Left ventricular ejection fraction at rest greater than 40%
    • Hepatic: Bilirubin less than 2 times the upper limit of normal and ALT and AST less than 3 times the upper limit of normal
    • Renal: Creatinine clearance greater than 40 ml/min (measured or calculated/estimated)
    • Pulmonary: DLCO, FEV1, and FVC greater than 50% of predicted value (corrected for hemoglobin), or O2 saturation greater than 92% of room air
  • An adequate autologous graft defined as a cryopreserved PBSC graft containing at least 4.0 x 10^6 CD34+ cells/kg patient weight; if prior to enrollment it is known that a patient will be on the auto-allo arm (i.e., a consenting, eligible HLA-matched sibling donor is available), the required autograft must contain at least 2.0 x 10^6 CD34+ cells/kg patient weight; the graft may not be CD34+ selected or otherwise manipulated to remove tumor or other cells; the graft can be collected at the transplanting institution or by a referring center; for patients without an HLA-matched sibling donor, the autograft must be stored so that there are two products each containing at least 2 x 10^6 CD34+ cells/kg patient weight

Exclusion Criteria:

  • Never advanced beyond Stage I MM since diagnosis
  • Non-secretory MM (absence of a monoclonal protein [M protein] in serum as measured by electrophoresis and immunofixation and the absence of Bence Jones protein in the urine defined by use of conventional electrophoresis and immunofixation techniques)
  • Plasma cell leukemia
  • Karnofsky performance score less than 70%, unless approved by the Medical Monitor or one of the Protocol Chairs
  • Uncontrolled hypertension
  • Uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms)
  • Prior malignancies except resected basal cell carcinoma or treated cervical carcinoma in situ; cancer treated with curative intent less than 5 years previously will not be allowed unless approved by the Medical Monitor or one of the Protocol Chairs; cancer treated with curative intent more than 5 years previously will be allowed
  • Pregnant or breastfeeding
  • Seropositive for the human immunodeficiency virus (HIV)
  • Unwilling to use contraceptive techniques during and for 12 months following treatment
  • Prior allograft or prior autograft
  • Received mid-intensity melphalan (more than 50 mg IV) as part of prior therapy
  • Prior organ transplant requiring immunosuppressive therapy

Sites / Locations

  • Hematology-Oncology & SCT Research CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Autologous arm

Allogeneic arm

Arm Description

Outcomes

Primary Outcome Measures

Overall Survival and Progressive Free Survival in both two arms

Secondary Outcome Measures

Overall Survival and Progressive Free Survival in both two arms
Treatment Related Mortality (TRM) in both two arms
Acute and Chronic GVHD in Allogeneic arm

Full Information

First Posted
October 17, 2009
Last Updated
May 31, 2012
Sponsor
Tehran University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT00998270
Brief Title
Autologous Bone Marrow Transplantation (BMT) Compared With Allogeneic BMT in Multiple Myeloma
Official Title
A Prospective, Randomized Trial of Autologous Bone Marrow Transplantation Compare With Allogeneic Bone Marrow Transplantation in Multiple Myeloma
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Unknown status
Study Start Date
October 2009 (undefined)
Primary Completion Date
October 2014 (Anticipated)
Study Completion Date
October 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tehran University of Medical Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A prospective, randomized trial of autologous bone marrow transplantation compared with allogeneic bone marrow transplantation in multiple myeloma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
MM

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
185 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Autologous arm
Arm Type
Active Comparator
Arm Title
Allogeneic arm
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Autologous bone marrow transplantation
Other Intervention Name(s)
Autologous
Intervention Description
Autologous transplantation: Endoxan (for mobilization) Dose: 2.5 g/m2 IV Time: -11 Duration: 1 day G-CSF (Neupogen) Dose: 0.5 micg/kg subcutaneous Time: -6 to -3 Duration: 4 days Melphalan Dose: 100 mg/m2 IV Time: -2 and -1 Duration: 2 days
Intervention Type
Procedure
Intervention Name(s)
Allogeneic bone marrow transplantation
Other Intervention Name(s)
Allogeneic
Intervention Description
Allogeneic Melphalan Dose: 70 mg/m2 IV Time: Duration: 2 days Fludarabine Dose: 30 mg/m2 IV Time: Duration: 5 days
Primary Outcome Measure Information:
Title
Overall Survival and Progressive Free Survival in both two arms
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall Survival and Progressive Free Survival in both two arms
Time Frame
3 year
Title
Treatment Related Mortality (TRM) in both two arms
Time Frame
3 year
Title
Acute and Chronic GVHD in Allogeneic arm
Time Frame
3 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age at diagnosis equal or under 55 year Meeting the Durie and Salmon criteria for initial diagnosis of MM Stage II or III MM at diagnosis or anytime thereafter Symptomatic MM requiring treatment at diagnosis or anytime thereafter If receiving chemotherapy-based mobilization regimens, must be able to receive high-dose melphalan between 2 and 8 weeks after the initiation of mobilization therapy whether delivered at the transplant center or at a referring center Adequate organ function as measured by: Cardiac: Left ventricular ejection fraction at rest greater than 40% Hepatic: Bilirubin less than 2 times the upper limit of normal and ALT and AST less than 3 times the upper limit of normal Renal: Creatinine clearance greater than 40 ml/min (measured or calculated/estimated) Pulmonary: DLCO, FEV1, and FVC greater than 50% of predicted value (corrected for hemoglobin), or O2 saturation greater than 92% of room air An adequate autologous graft defined as a cryopreserved PBSC graft containing at least 4.0 x 10^6 CD34+ cells/kg patient weight; if prior to enrollment it is known that a patient will be on the auto-allo arm (i.e., a consenting, eligible HLA-matched sibling donor is available), the required autograft must contain at least 2.0 x 10^6 CD34+ cells/kg patient weight; the graft may not be CD34+ selected or otherwise manipulated to remove tumor or other cells; the graft can be collected at the transplanting institution or by a referring center; for patients without an HLA-matched sibling donor, the autograft must be stored so that there are two products each containing at least 2 x 10^6 CD34+ cells/kg patient weight Exclusion Criteria: Never advanced beyond Stage I MM since diagnosis Non-secretory MM (absence of a monoclonal protein [M protein] in serum as measured by electrophoresis and immunofixation and the absence of Bence Jones protein in the urine defined by use of conventional electrophoresis and immunofixation techniques) Plasma cell leukemia Karnofsky performance score less than 70%, unless approved by the Medical Monitor or one of the Protocol Chairs Uncontrolled hypertension Uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms) Prior malignancies except resected basal cell carcinoma or treated cervical carcinoma in situ; cancer treated with curative intent less than 5 years previously will not be allowed unless approved by the Medical Monitor or one of the Protocol Chairs; cancer treated with curative intent more than 5 years previously will be allowed Pregnant or breastfeeding Seropositive for the human immunodeficiency virus (HIV) Unwilling to use contraceptive techniques during and for 12 months following treatment Prior allograft or prior autograft Received mid-intensity melphalan (more than 50 mg IV) as part of prior therapy Prior organ transplant requiring immunosuppressive therapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ardeshir Ghavamzadeh, MD
Phone
84902635
Ext
+98-21
Email
ghavamza@sina.tums.ac.ir
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ardeshir Ghavamzadeh, MD
Organizational Affiliation
Hematology-Oncology and SCT Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hematology-Oncology & SCT Research Center
City
Tehran
Country
Iran, Islamic Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ardeshir Ghavamzadeh, MD
Phone
84902635
Ext
+98-21
Email
ghavamza@sina.tums.ac.ir
First Name & Middle Initial & Last Name & Degree
Ardeshir Ghavamzadeh, MD
First Name & Middle Initial & Last Name & Degree
Kamran Alimoghaddam, MD
First Name & Middle Initial & Last Name & Degree
Mahdi Jalili, MD

12. IPD Sharing Statement

Learn more about this trial

Autologous Bone Marrow Transplantation (BMT) Compared With Allogeneic BMT in Multiple Myeloma

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