Phase 3
N=224
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
Bottom Line
View on ClinicalTrials.gov: NCT00412360 ↗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
| Outcome | Result | p-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
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.