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Phase 3 N=224 Randomized Treatment

Single vs Double Umbilical Cord Blood Transplants in Children With High Risk Leukemia and Myelodysplasia (BMT CTN 0501)

Acute Myelogenous Leukemia · Acute Lymphocytic Leukemia · Chronic Myelogenous Leukemia · Myelodysplastic Syndrome · Natural Killer Cell Lymphoblastic Leukemia/Lymphoma

Enrolled (actual)
224
Serious AEs
8.6%
Results posted
Dec 2015
Primary outcome: Primary: Percentage of Participants With Overall Survival — 73; 65 percentage of participants — p=0.17

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Single Umbilical Cord Blood Unit Transplant (Biological); Double Umbilical Cord Blood Unit Transplant (Biological); Total Body Irradiation (Radiation); Cyclophosphamide (Drug); Fludarabine (Drug); Cyclosporine A (Drug); Mycophenolate Mofetil (Drug)
Age
Pediatric, Adult · 1+ yrs
Sex
All
Sponsor
Medical College of Wisconsin
Primary completion
Mar 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With Overall Survival
73; 65 0.17
SECONDARY
Percentage of Participants With Disease-free Survival
70; 64 0.11
SECONDARY
Percentage of Participants With Neutrophil and Platelet Engraftment
89; 88; 76; 65 0.29
SECONDARY
Time to Neutrophil and Platelet Engraftment
21; 23; 58; 84
SECONDARY
Percentage of Participants With Acute Graft-versus-host Disease (GVHD)
57; 56; 13; 23 0.78
SECONDARY
Percentage of Participants With Chronic GVHD
30; 32; 9; 15 0.51
SECONDARY
Number of Infections Per Participant
10; 9; 15; 13; 12; 15
SECONDARY
Percentage of Participants With Relapse
12; 14 0.12
SECONDARY
Percentage of Participants With Treatment-related Mortality
19; 22 0.43
SECONDARY
Number of Participants With Engraftment Syndrome
11; 7

Summary

This study is a Phase III, randomized, open-label, multi-center, prospective study of single umbilical cord blood (UCB) transplantation versus double UCB transplantation in pediatric patients with hematologic malignancies.

Eligibility Criteria

Inclusion Criteria

  • Two partially HLA-matched UCB units. Units must be HLA-matched minimally at 4 of 6 HLA-A and B (at intermediate resolution by molecular typing) and DRB1 (at high resolution by molecular typing) loci with the patient, and the units must be HLA-matched at 3 of 6 HLA- A, B, DRB1 loci with each other (using same resolution of molecular typing as indicated above). Two appropriately HLA-matched units must be available such that one unit delivers a pre-cryopreserved nucleated cell dose of at least 2.5 x 10^7 per kilogram and the second unit at least 1.5 x 10^7 per kilogram.
  • Acute myelogenous leukemia (AML) at the following stages:
  • High risk first complete remission (CR1), defined as the following:
  • Having preceding myelodysplasia (MDS)
  • High risk cytogenetics (high risk cytogenetics: del (5q) -5, -7, abn (3q), t (6;9) complex karyotype [at least 5 abnormalities],)the presence of a high FLT3 ITD-AR (> 0.4)
  • Requiring more than 1 cycle of chemotherapy to obtain complete remission (CR);
  • FAB M6
  • Second or greater CR
  • First relapse with less than 25% blasts in bone marrow
  • Morphologic complete remission with incomplete blood count recovery
  • Therapy-related AML for which prior malignancy has been in remission for at least 12 months
  • Acute lymphocytic leukemia (ALL) at the following stages:
  • High risk first remission, defined as one of the following conditions:
  • Philadelphia chromosome-positive adult lymphoblastic leukemia (Ph+ ALL)
  • Mixed lineage leukemia (MLL) rearrangement with slow early response (defined as having M2 [5-25% blasts] or M3 [more than 25% blasts on bone marrow examination on Day 14 of induction therapy])
  • Hypodiploidy (less than 44 chromosomes or DNA index less than 0.81)
  • End of induction M3 bone marrow
  • End of induction M2 with M2-3 at Day 42
  • Evidence of minimal residual disease (MRD). If a patient's only high risk criterion is MRD, approval by a protocol chair or protocol officer is required for enrollment. For COG centers, this will only be for MRD greater than 1 percent by flow MRD at the end of extended induction.
  • High risk second remission, defined as one of the following conditions:
  • Philadelphia chromosome-positive adult lymphoblastic leukemia (Ph+ ALL)
  • Bone marrow relapse less than 36 months from induction
  • T-lineage relapse at any time
  • Very early isolated central nervous system (CNS) relapse (6 months from diagnosis)
  • Slow reinduction (M2-3 at Day 28) after relapse at any time
  • Evidence of minimal residual disease (MRD). If a patient's only high risk criterion is MRD, approval by a protocol chair or protocol officer is required for enrollment. For COG centers, this will only be for MRD greater than 1 percent by flow MRD at the end of extended induction.
  • Any third or subsequent CR
  • NK cell lymphoblastic leukemia in any CR
  • Biphenotypic or undifferentiated leukemia in any CR or if in first relapse must have less than 25% blasts in bone marrow (BM)
  • Myelodysplastic syndrome (MDS) at any stage
  • Chronic myelogenous leukemia (CML) in chronic or accelerated phase
  • All patients with evidence of CNS leukemia must be treated and be in CNS CR to be eligible for study.
  • Patients 16 years old or older must have a Karnofsky score of at least 70% and patients younger than 16 years old must have a Lansky score of at least 70%.
  • Patients with adequate physical function as measured by:
  • Cardiac: Left ventricular ejection fraction greater than 40% or shortening fraction greater than 26%
  • Hepatic: Bilirubin no more than 2.5 mg/dL; alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) no more than 5 times the upper limit of normal (ULN)
  • Renal: Serum creatinine within normal range for age, or if serum creatinine is outside normal range for age, then renal function (creatinine clearance or GFR) greater than 70 mL/min/1.73 m^2
  • Pulmonary: Diffusing capacity of the lung for carbon monoxide (DLCO), forced expi
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00412360). 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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