Intraosseous Infusion of Unrelated Cord Blood Grafts

This study has been terminated.
(poor enrollment)
Sponsor:
Information provided by (Responsible Party):
John Horan, Emory University
ClinicalTrials.gov Identifier:
NCT00967525
First received: August 11, 2009
Last updated: November 3, 2011
Last verified: November 2011

August 11, 2009
November 3, 2011
March 2007
July 2011   (final data collection date for primary outcome measure)
Compare the rapidity of myeloid engraftment of intraosseously and intravenously administered unrelated cord blood grafts. [ Time Frame: 1 year after last patient enrolled ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00967525 on ClinicalTrials.gov Archive Site
Obtain preliminary data using flow cytometric analysis to assess the importance of graft associated variables that may affect engraftment. [ Time Frame: 1 year after last patient enrolled ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Intraosseous Infusion of Unrelated Cord Blood Grafts
A Pilot Study of Intraosseous Infusion of Unrelated Cord Blood Grafts

In this trial the investigators seek to determine if injecting cord blood cells directly into the bone marrow (intraosseous injection), rather than infusing them intravenously, can improve engraftment. The rational for doing this is that most hematopoietic stem cells (HSCs) infused intravenously never reach the bone marrow, getting trapped by other organs, such as the lungs, instead. The potential advantage of intraosseous infusion is suggested by studies in rodents that have demonstrated that in HSC transplants where the cell dose is limiting intraosseous injection is a more effective route of administration. The safety of intraosseous injections, in general, is underscored by the vast experience using intraosseous injections for resuscitation of critically ill children. The safety of injecting HSCs intraosseously has been demonstrated in a clinical trial of transplanting bone marrow cells.

To safeguard against problems that might result, if intraosseous infusion fails to improve engraftment in this trial, the investigators will integrate a recently introduced strategy proven to improve engraftment-the transplantation of two cord blood units. Transplanting two unrelated cord blood units by intravenous infusion has been shown to improve engraftment (although there is still room for improvement). In this trial one unit will be injected intraosseously and the other unit will be infused intravenously.

This study is being conducted as a forerunner to a larger, multi-center trial. The investigators intend to enroll five patients over 1-2 years.

Hematopoietic (blood forming) stem cells (HSCs) reside primarily in the bone marrow. Traditionally, HSCs have been obtained directly from the bone marrow. Transplants using cells obtained this way are referred to as bone marrow transplants. HSCs also circulate in the blood. Transplants using cells obtained from the blood of children and adults are referred to as peripheral blood stem cell transplants. The blood of fetuses is especially rich in HSCs and these cells can be easily collected at birth from the placenta. Transplants using these cells are called cord blood transplants. Although HSCs can be collected from various sites, all HSC transplants, regardless of the source, are given to recipients by intravenous infusion. The transplanted HSCs then migrate to the bone marrow.

Over the past ten years unrelated cord blood transplantation has become an accepted alternative to bone marrow transplantation. African-Americans and other minorities, who are underrepresented in the National Marrow Donor Program, have benefited particularly from this. In infants and young children cord blood transplantation appears to be as effective as bone marrow transplantation. In older children, adolescents and adults, however, cord blood transplantation has not been as effective, primarily because most cord blood units provide an insufficient number of cells to ensure prompt and reliable engraftment ("taking" of the transplanted cells in the recipient's bone marrow).

Interventional
Not Provided
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Acute Myeloid Leukemia
  • Acute Lymphoblastic Leukemia
  • Chronic Myelogenous Leukemia
  • Myelodysplastic Syndrome
Procedure: cord blood infusion
Receive two cord blood units. One administered by intraosseous infusion and the other by intravenous infusion. The second unit is being given as a safeguard, but will also allow the researchers to directly compare engraftment between intravenously and intraosseously infused cord blood units.
Experimental: 1
Receive two cord blood units. One administered by intraosseous infusion and the other by intravenous infusion. The second unit is being given as a safeguard, but will also allow the researchers to directly compare engraftment between intravenously and intraosseously infused cord blood units.
Intervention: Procedure: cord blood infusion
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
6
July 2011
July 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Age 36 months to 60 years old (YO)
  2. No prior autologous or allogeneic transplant
  3. Karnofsky performance score or Lansky Play-Performance of at least 80

Exclusion Criteria:

  1. Age < 36 months or > 60 YO
  2. creatinine clearance or nuclear medicine GFR of < 50 mL/min
  3. cardiac ejection fraction < 50%
  4. bilirubin > 2 × upper limit of normal or ALT > 4 × upper limit of normal or unresolved veno-occlusive disease
  5. Pulmonary carbon monoxide diffusing capacity (DLCO), adjusted for Hgb < 50%
  6. Karnofsky performance score or Lansky Play-Performance Scale <80
  7. Uncontrolled viral, bacterial, or fungal infection at the time of study enrollment
  8. Seropositive for HIV
  9. Availability of a willing and well HLA matched related (genotypically identical or mismatched at a single allele or antigen defined by typing at HLA A, B, C and DRB1 loci) donor
  10. Availability of a willing and well HLA matched unrelated (allele matched or mismatched at a single allele defined by allele level typing for HLA A, B, C and DRB1 loci) adult blood or marrow donor
  11. Availability of an umbilical cord blood unit, which provides at least a 4/6 HLA match as defined above and ≥ 5.0 * 107 NC/Kg (cryopreserved)
Both
36 Months to 60 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00967525
Intraosseous Infusion
Yes
John Horan, Emory University
Emory University
Not Provided
Principal Investigator: John Horan, MD Emory University
Emory University
November 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP