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Clinical Trials/NCT00676806
NCT00676806
Terminated
Phase 2

A Phase II Study of Umbilical Cord Blood Transplantation Following Myeloablative or Reduced-Intensity Conditioning

Tufts Medical Center1 site in 1 country7 target enrollmentJuly 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Leukemia
Sponsor
Tufts Medical Center
Enrollment
7
Locations
1
Primary Endpoint
Number of Participants With Neutrophil Engraftment
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

This study is designed to determine whether Umbilical Cord Transplantation (UCB) can be substituted for adult bone marrow cells in the standard stem cell transplant regimens used at this hospital for subjects who do not have stem cell donors.

Detailed Description

Allogeneic stem cell transplantation (SCT) following myeloablative and non-myeloablative conditioning therapy has proven curative treatment for a number of inherited and acquired hematologic disorders. The success of allogeneic transplantation is largely determined by compatibility between donor and recipient, which predicts the risk of fatal graft-versus-host disease (GVHD). Unfortunately, less than one third of patients needing an allogeneic transplant have an available compatible donor in their family. Registries have been established to match patients with compatible volunteer (unrelated) donors, but many patients, and in particular minority patients, still lack stem cell donors. Umbilical cord blood (UCB) is a rich source of hematopoietic stem cells, which is readily available from the placenta following childbirth. Blood banks have been established in the United States and abroad to collect, process and store UCB for use in allogeneic transplantation. To date, more than 2000 UCB transplants have been performed in adults and children around the world. Rationale for use of Umbilical Cord Blood in Transplantation UCB has a number of proven and theoretical advantages as an alternative source of hematopoietic stem cells for transplantation: 1. Placental or umbilical cord blood is an abundantly available source of stem cells, which is currently discarded and can be harvested at no risk to the mother or infant. 2. Important infectious agents, particularly CMV, are much less common in the newborn than adults, and are less likely to contaminate UCB collections. 3. UCB collections, typed, cryopreserved and banked, are available on demand, eliminating delays and uncertainties that now complicate marrow collection from unrelated donors. At present, UCB can be delivered for infusion within days of the initiation of a search. This compares with a median of 3 months from search to delivery of stem cells through the registries of volunteer adult donors. 4. The intensity of graft-versus-host reactivity of fetal lymphocytes appears to be less than that of adult cells and consequently fetal lymphocytes are more tolerant of HLA incompatibility. Published studies have shown that transplantation of UCB matched at 4-5/6 antigens results in a comparable incidence of GVHD to transplantation of unrelated stem cells fully matched at 6/6 antigens. 5. Frozen UCB can be easily shipped, stored at the treating institution, and thawed for use when needed, compared to freshly donated stem cells which have a limited shelf-life of one day or less, necessitating coordination between harvesting surgeons, transportation, and transplantation teams. This research study has been designed for people who have been diagnosed with a blood tumor, which has not responded to treatment or has recurred, a bone marrow failure state such as aplastic anemia, or one of certain inherited metabolic disorders; and whose doctor feels the best treatment is an allogeneic stem cell transplant (alloSCT) but a related or unrelated adult donor is not available. Instead, a single unit of umbilical cord blood (UCB) will be used as the source of the subject's immune system. This study is designed to determine whether a single unit of UCB can be substituted for adult bone marrow cells in the standard stem cell transplant regimens used at this hospital for subjects who do not have stem cell donors.

Registry
clinicaltrials.gov
Start Date
July 2005
End Date
July 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients meeting eligibility criteria for unrelated allogeneic stem cell transplantation may be considered for participation on this clinical trial if and only if they meet each of the following criteria:
  • Patients must have one of the following diagnoses
  • Relapsed or refractory hematologic malignancy, or
  • High risk hematologic malignancy in first remission, or
  • Refractory acquired marrow failure state, or
  • Inherited disorder of metabolism or marrow failure state without alternative curative therapy.
  • Patients must not have a 6/6 or 5/6 HLA-matched related donor.
  • Patients must not have a HLA-A, -B and -DRB1 high resolution matched unrelated donor following registry search, or cannot (in the opinion of the treating physician) wait the median 3 months to receive a MUD unit.
  • Patients must demonstrate an ability to understand and willingness to sign the informed consent document
  • Patients considered for myeloablative conditioning must satisfy the following additional criteria:

Exclusion Criteria

  • Patients are ineligible for participation on this trial if they meet any of the following criteria:
  • Patients with a history of myocardial infarction within the preceding 6 months, significant arrhythmia within the preceding 3 months, uncontrolled hypertension or congestive heart failure are ineligible.
  • Patients with unstable angina are not eligible.
  • Pregnant or lactating women are ineligible.
  • Male and female patients who do not agree to practice approved methods of birth control for the duration of the study are ineligible.
  • Patients with uncontrolled infection are ineligible.
  • Patients who are HIV positive or have evidence of chronic viral hepatitis are ineligible.
  • Patients unable to comply with requirements for compliance with therapeutic plan and/or scheduled evaluations

Outcomes

Primary Outcomes

Number of Participants With Neutrophil Engraftment

Time Frame: +45 and 90 days

Number of participants with neutrophil engraftment receiving umbilical cord blood for hematopoietic rescue following myeloablative or non-myeloablative conditioning

Secondary Outcomes

  • Proportion of Subjects With Platelet Engraftment(+45, 90, and 180 days)
  • Incidence of Acute GVHD(Day +100)
  • Infectious Complications in UCB Recipients.(Day +100)
  • Incidence of Chronic GVHD(After Day +100)
  • Compare Rates of Complications Between Patients Receiving Ablative vs. Non-myeloablative Conditioning Prior to UCB Transplantation(+180 days)

Study Sites (1)

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