Intra Bone Marrow Injection Of Unrelated Cord Blood Cells (CB01)
Primary Purpose
Hematologic Diseases
Status
Unknown status
Phase
Phase 1
Locations
Italy
Study Type
Interventional
Intervention
Intrabone Marrow Injection
Sponsored by
About this trial
This is an interventional treatment trial for Hematologic Diseases focused on measuring CORD BLOOD CELLS, INTRA BONE MARROW INJECTION, ENGRAFTMENT, transplants
Eligibility Criteria
Inclusion Criteria:
- Patients with hematologic malignancies and other forms of hematologic diseases including aplastic anemia
- Patients will be eligible to enter the study when: A) an unrelated stem cell transplantation was indicated; b) no suitable unrelated HLA-matched donors will be identified in a clinically useful time-frame.
- Age 16-70
- Serum creatinine <1.5 mg/dL or Creatinine Clearance >50 ml/min
- Serum bilirubin <1.5 mg/dl, SGPT <3 x upper limit of normal
- Negative serology for HIV
- Central Venous access (Central KT) secured through an indwelling catheter.
- Life expectancy is not severely limited by concomitant illness.
- Written and signed informed consent
Exclusion Criteria:
- Acute Myocardial Infarction (AMI) within the last 12 months
- Positive pregnancy test
- Positive HIV serology
- Chronic renal insufficiency (Serum creatinine >1.5 mg/dl or creatinine cleareance <=50 ml/min)
- Patient has another progressive malignant disease or a history of other malignancies within 2 years prior to study entry.
- Severe psychiatric illness or any disorder that compromises ability to give truly informed consent for participation in this study.
Sites / Locations
- A.O. San Martino - Dep. Center Stem cells and cell therapy"Recruiting
Outcomes
Primary Outcome Measures
the safety and the probability of neutrophils and platelets recovery after i.b. cord blood transplant.
Secondary Outcome Measures
the incidence/severity of acute Graft-versus-Host Disease, relapse and overall survival.
Full Information
NCT ID
NCT00696046
First Posted
June 9, 2008
Last Updated
June 9, 2008
Sponsor
IRCCS Azienda Ospedaliera Universitaria San Martino - IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy
1. Study Identification
Unique Protocol Identification Number
NCT00696046
Brief Title
Intra Bone Marrow Injection Of Unrelated Cord Blood Cells
Acronym
CB01
Official Title
Direct Intra Bone Marrow Injection Of Unrelated Cord Blood Cells To Improve Engraftment And Reduce Acute Graft-Versus-Host Disease
Study Type
Interventional
2. Study Status
Record Verification Date
June 2008
Overall Recruitment Status
Unknown status
Study Start Date
March 2006 (undefined)
Primary Completion Date
December 2008 (Anticipated)
Study Completion Date
June 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
IRCCS Azienda Ospedaliera Universitaria San Martino - IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Compared to other stemcell sources cord blood (CB) is easier and safer to procure, has no donor attrition, a limitless supply, reduced viral transmission, less acute & chronic GVHD, is rich in hematopoietic progenitor cells, and immaturity of T-cell-mediated immunity. CB has delayed neutrophil and platelet engraftment, a prolonged immune reconstitution, uncertain graft-vs-tumor activity, and cell doses from single CB units (U) are a limiting factor for larger recipients Using the intravenous route (IV), a close match between the patient (pts) and the donor or CBU can improve a pts outcome after transplant. Even though a closely matched CBU is preferred, the studies suggest the match may not have to be as close as is needed for marrow or peripheral blood transplants If one has an uncommon tissue type, the doctor may not find a closely matched adult donor and a CBU may be an option, are stored and ready to use. GVHD is a complication after an allogeneic transplant. Studies founded that after a CBtransplant, fewer pts get GVHD than after marrow or peripheral blood transplants. Pts in the studies who did get GVHD after CBtransplant tended to get less severe cases We hypothesized that direct intrabone transplant of CBcells could improve haematologic recovery due to a better stem cell homing, based on the following observations: stem cells recirculate in animals irradiated with limb shielding; a limited fraction (10-15%) of cells injected iv to the haematopoietic sites, possibly because the large majority is lost in other organs; in a mousemodel, HSC directly injected ib repopulated the marrow of lethally irradiated mice 10times more efficiently than HSC cells injected iv; delayed engraftment after CB transplant is possibly not caused by insufficient stem cell numbers; indeed, children grafted with CB cells have superior stem cell reservoir 1year posttransplant when compared to marrow transplant recipients Based on these data, we set-up a phase I-II study to evaluate whether ib injection could be safely performed and whether this procedure could ensure engraftment and shorten the time of complete hematopoietic recovery in adults with high risk haematopoietic malignancies compared to the published data. Neutrophil recovery >80% at day60 and Platelets recovery >80% at days100 were defined as success. 1° endpoint was the probability of neutrophils and platelets recovery after ib CB transplant, 2° included incidence of acute GVHD, relapse, overall survival
Detailed Description
Study Design Phase I-II study. Neutrophil recovery > 80% at day 60 and Platelets recovery > 80% at days 100 are defined as success. The limit of 60 days for neutrophil recovery was chosen because it represents the time at which rescue with a second transplant is decided in case of failure to engraft; the day 100 for platelets recovery is taken corresponds to first form reported after transplant to the European Blood and Marrow Transplant Registry.
HLA-A and -B antigens will be identified by low resolution DNA typing, whereas HLA-DRB1 type was determined by high resolution DNA typing techniques. HLA-A, HLA-B, and HLA-DRB1 typing was used to select the most closely matched donor unit-recipient pair, with preference given to HLA-DRB1-matched unit
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hematologic Diseases
Keywords
CORD BLOOD CELLS, INTRA BONE MARROW INJECTION, ENGRAFTMENT, transplants
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
47 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Intrabone Marrow Injection
Intervention Description
Cord blood CB units will be thawed in a 37° CB cells will be resuspended in 20ml salinesolution + dextran/albumin, and aliquoted in 4 syringes of 5ml Pts were prepared in a surgical & steril room The anaesthesia consist in a short propofol sedation The injection will last 8-15 minutes. 1° sedation is established, a standard needle for bone marrow aspiration (14 gauge) was inserted few cms in the supero-posterior iliac crest then, an aspiration of about 0.5-1 ml will be performed to assess that the needle was securely introduced in the bone marrow cavity After, we will insert the syringe containing 4-5ml of CB cell suspension which will be gently infused This procedure will be then repeated for all the remaining aliquots at a distance of 2-3cm from the previous one following the iliac crest
Primary Outcome Measure Information:
Title
the safety and the probability of neutrophils and platelets recovery after i.b. cord blood transplant.
Time Frame
Full blood count, Monitoring Infections post Transplant, Bone marrow evaluation, Chimerism Analysis, Haematopoietic Reconstitution
Secondary Outcome Measure Information:
Title
the incidence/severity of acute Graft-versus-Host Disease, relapse and overall survival.
Time Frame
Graft-versus-host disease was scored according to current criteria (13).
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with hematologic malignancies and other forms of hematologic diseases including aplastic anemia
Patients will be eligible to enter the study when: A) an unrelated stem cell transplantation was indicated; b) no suitable unrelated HLA-matched donors will be identified in a clinically useful time-frame.
Age 16-70
Serum creatinine <1.5 mg/dL or Creatinine Clearance >50 ml/min
Serum bilirubin <1.5 mg/dl, SGPT <3 x upper limit of normal
Negative serology for HIV
Central Venous access (Central KT) secured through an indwelling catheter.
Life expectancy is not severely limited by concomitant illness.
Written and signed informed consent
Exclusion Criteria:
Acute Myocardial Infarction (AMI) within the last 12 months
Positive pregnancy test
Positive HIV serology
Chronic renal insufficiency (Serum creatinine >1.5 mg/dl or creatinine cleareance <=50 ml/min)
Patient has another progressive malignant disease or a history of other malignancies within 2 years prior to study entry.
Severe psychiatric illness or any disorder that compromises ability to give truly informed consent for participation in this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
francesco Frassoni, MD
Phone
+39 010 5553961
Ext
3941
Email
francesco.frassoni@hsanmartino.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
francesco frassoni, MD
Organizational Affiliation
A.O. San martino
Official's Role
Principal Investigator
Facility Information:
Facility Name
A.O. San Martino - Dep. Center Stem cells and cell therapy"
City
Genoa
ZIP/Postal Code
16132
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
francesco frassoni, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
18693069
Citation
Frassoni F, Gualandi F, Podesta M, Raiola AM, Ibatici A, Piaggio G, Sessarego M, Sessarego N, Gobbi M, Sacchi N, Labopin M, Bacigalupo A. Direct intrabone transplant of unrelated cord-blood cells in acute leukaemia: a phase I/II study. Lancet Oncol. 2008 Sep;9(9):831-9. doi: 10.1016/S1470-2045(08)70180-3. Epub 2008 Aug 8.
Results Reference
derived
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Intra Bone Marrow Injection Of Unrelated Cord Blood Cells
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