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N/A N=16 Treatment

Umbilical Cord Blood Transplant for Children With Myeloid Hematological Malignancies

Myeloid Hematological Malignancies

Enrolled (actual)
16
Serious AEs
68.8%
Results posted
Jun 2022
Primary outcome: Primary: Overall Survival at 100 Days, 1 Year, and 3 Years After Umbilical Cord Blood Transplant in Pediatric Patients. — 0.923; 0.923; 0.923 probability of overall survival

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Busulfan (Drug); Cyclophosphamide (Drug); Fludarabine (Drug); Cord Blood Stem Cell Infusion (Procedure)
Age
Pediatric
Sex
All
Sponsor
Baylor College of Medicine
Primary completion
Oct 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Survival at 100 Days, 1 Year, and 3 Years After Umbilical Cord Blood Transplant in Pediatric Patients.
0.923; 0.923; 0.923
SECONDARY
Number of Participants With Severe Acute GVHD Grade III-IV
2
SECONDARY
Number of Participants With Chronic GvHD
1
SECONDARY
Number of Participants With Relapse Rate After Transplant
53.3; 53.3
SECONDARY
Number of Participants With Donor Engraftment After Transplant.
11; 6; 6; 6; 6; 3
SECONDARY
Number of Participants With Platelet Engraftment
13
SECONDARY
Number of Participants With Neutrophil Engraftment
15

Summary

In this study, the investigators will use busulfan and cyclophosphamide (BuCy) backbone with the addition of fludarabine as the preparative Stem Cell Transplant (SCT) regimen. As an attempt to improve engraftment rate and reduce infections, the investigators are going to incorporate fludarabine in the conditioning regimen. The use of a BuCy backbone has been widely used and comparable to total body irradiation and cyclophosphamide (Cy/TBI) regimen. Encouraging data on adding fludarabine to the SCT regimen have been reported. A fludarabine-based, conditioning regimen, with adequate immunosuppressive activity could conceivably allow engraftment of stem cells from alternative donors in hematologic malignancies patients with acceptable engraftment rates and low transplant-related mortality. Regimen-related toxicity is believed to be a major contributing factor to GVHD. Therefore this approach may also lead to reduced GVHD, as some investigators have suggested. In an attempt to decrease the rate of viral infection and reactivation, the investigators will avoid ATG (Thymoglobulin) / Campath (anti-CD52), and instead administer Mycophenolate Mofetil (MMF). The addition of fludarabine should compensate any increase risk of graft failure with the removal of the ATG/Campath. The investigators anticipate that the removal of ATG/Campath will facilitate immune reconstitution more efficiently after receiving a UCBT.

Eligibility Criteria

Inclusion Criteria

  • Patients with a myeloid hematologic malignancy (acute myelogenous leukemia, secondary myelogenous leukemia or myelodysplastic syndrome) unlikely to be cure by standard chemotherapy. This includes patients who have relapsed after standard chemotherapy treatments and patients in first remission with unfavorable prognostics features.
  • Related or Unrelated Umbilical Cord Blood Unit with 0-1 antigen mismatch at HLA-A and B (at low resolution) and DRB1 (at high resolution), with a total nucleated cell dose of ≥ 4 x 10^7/kg.
  • Lansky/Karnofsky scores at least 60.
  • Written informed consent and/or signed assent line from patient, parent or guardian.
  • Negative pregnancy test, if applicable.

Exclusion Criteria

  • Patients with uncontrolled infections. For bacterial infections, patients must be receiving definitive therapy and have no signs of progressing infection for 72 hours prior to enrollment. For fungal infections, patients must be receiving definitive systemic antifungal therapy and have no signs of progressing infection for 1 week prior to enrollment. Progressing infection is defined as hemodynamic instability attributable to sepsis or new symptoms, worsening physical signs or radiographic findings attributable to infection. Persisting fever without other signs or symptoms will not be interpreted as progressing infection.
  • Severe renal disease (Creatinine > 3X normal for age).
  • Severe hepatic disease (direct bilirubin > 3 mg/dL or SGOT > 500).
  • Patient has DLCO < 50% predicted or FEV1 < 50% of predicted, if applicable.
  • Patients with symptomatic cardiac failure unrelieved by medical therapy or evidence of significant cardiac dysfunction by echocardiogram (shortening fraction < 20%).
  • HIV positive.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01247701). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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