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Phase 2 N=32 Treatment

Myeloablative Haploidentical BMT With Post-transplant Cyclophosphamide for Pediatric Patients With Hematologic Malignancies

Myeloablative Conditioning · HLA-mismatched Bone Marrow Transplantation · Graft Survival · Transplantation, Bone Marrow

Enrolled (actual)
32
Serious AEs
43.8%
Results posted
Apr 2019
Primary outcome: Primary: Cumulative Incidence of Non-relapse Mortality — 0 percent

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Cyclophosphamide (Drug); TBI (Radiation); Busulfan (Drug); Unmanipulated Bone Marrow (Other); Tacrolimus (Drug); Mycophenolate mofetil (Drug)
Age
Pediatric, Adult · 0+ yrs
Sex
All
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Primary completion
Jun 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Cumulative Incidence of Non-relapse Mortality
SECONDARY
Number of Participants With Donor Cell Engraftment
27
SECONDARY
Cumulative Incidence of Acute Graft Versus Host Disease (GVHD) Grades 2-4 and Grades 3-4
10; 0
SECONDARY
Cumulative Incidence of Chronic GVHD
11
SECONDARY
Primary and Secondary Graft Failure
16; 0
SECONDARY
Steroid and Non-steroid Immunosuppressants
4; 2
SECONDARY
Steroid and Non-steroid Immunosuppressants Use Duration
18; 19
SECONDARY
Survival
73; 64; 64; 64; 52
SECONDARY
Survival
73; 64; 64; 64; 52
SECONDARY
Immune Reconstitution
SECONDARY
Time to Neutrophil and Platelet Recovery
22; 21
SECONDARY
Incidence of Donor Cell Engraftment
84

Summary

This is a multi-institutional phase II haploidentical T cell replete bone marrow transplant (BMT) study in children with high-risk leukemia. The myeloablative conditioning regimen prescribed will be Total body irradiation (TBI)-based for lymphoid leukemia and busulfan-based for myeloid leukemia. Our goal is to establish an easily exportable, inexpensive platform for haplotransplantation that has a safety profile equivalent to matched related and unrelated BMTs. The primary objective will be to estimate the incidence of 6-month non-relapse mortality (NRM), hypothesizing that NRM is < 18%.

Eligibility Criteria

Inclusion Criteria

  • Patient age 0.5-25years
  • Patients must have a first-degree related donor or half-sibling who is at minimum HLA haploidentical. The donor and recipient must be identical at at least one allele of each of the following genetic loci: HLA-A, HLA-B, HLA-Cw, HLA-DRB1, and HLA-DQB1. A minimum match of 5/10 is therefore required, and will be considered sufficient evidence that the donor and recipient share one HLA haplotype.
  • An unrelated donor search is not required for a patient to be eligible for this protocol, or a donor search and donor mobilization may be abandoned if the clinical situation dictates an urgent transplant. Clinical urgency is defined as 6-8 weeks from referral to transplant or a low-likelihood of finding a matched, unrelated donor. Patients with an eligible HLA-matched RELATED should not be enrolled on this trial.
  • Patients must have at least one of the following high-risk conditions listed below:
  • Acute lymphocytic leukemia (ALL) in CR1* as defined by at least one of the following:

hypodiploidy, induction failure,Minimal residual disease (MRD) after consolidation

  • Acute myeloid leukemia (AML) in CR1 with high risk features defined as: High allelic ratio FLT3/ITD+, Monosomy 7, Del (5q), Standard risk cytogenetics with positive minimal residual disease at the end of Induction I chemotherapy (for patients being treated on or according to Children's Oncology Group (COG) AAML1031 study who have had MRD studies sent to Seattle or performed at their local institution where the flow assay is sensitive enough to detect > 0.1% blasts)
  • Acute Leukemia in 2nd or subsequent CR (CR>2)
  • Mixed phenotype/Undifferentiated Leukemia in 1st or subsequent CR*
  • Secondary or therapy related leukemia in CR > 1
  • Natural Killer (NK) cell lymphoblastic leukemia CR > 1
  • Myelodysplastic syndrome (MDS)
  • Juvenile myelomonocytic leukemia (JMML) (patients are eligible if they are not eligible for COG1221 study)
  • Prior transplant eligible if 6 months has elapsed since BMT, and patient is off immunosuppression for > 3 months with no Graft versus host disease (GVHD)
  • No known active Central nervous system (CNS) involvement or extramedullary involvement by malignancy. Such disease treated into remission is permitted.
  • Acute Leukemia - Remission is defined as morphology with 20% cellularity.

Exclusion Criteria

  • Poor cardiac function: left ventricular ejection fraction 2 mg/dl (not due to hemolysis, Gilbert's or primary malignancy). Alanine aminotransferase (ALT) or Aspartate transaminase (AST) > 3 x laboratory upper normal limits.
  • Poor renal function: Creatinine >2.0mg/dl or creatinine clearance (calculated creatinine clearance is permitted) < 60 mL/min based on Traditional Cockcroft-Gault formula: 140 - age (yrs) x Smaller of Actual Weight vs. Ideal Body Weight (kg) / 72 x Serum creatinine (mg/dl) Multiply by another factor of 0.85 if female Intended for ages 18-110, serum creatinine 0.6-7 mg/dl For patients <18 years: creatinine clearance (CrCl) will be estimated by the Schwartz formula. A measured CrCl or a Glomerular filtration rate (GFR) may be substituted to determine the subject's CrCl.
  • Schwartz equation: CrCl (ml/min/1.73m2)=[length (cm) x k] /serum creatinine K = 0.45 for infants 1 to 52 weeks old k = 0.55 for children 1 to 13 years old k = 0.55 for adolescent females 13-18 years old k = 0.7 for adolescent males 13-18 years old
  • HIV-positive
  • Positive leukocytotoxic crossmatch Specifically, complement dependent cytotoxicity and flow cytometric crossmatch assays must be negative, and the mean fluorescence intensity (MFI) of any anti-donor HLA antibody by solid phase immunoassay should be <3000. Consult with PI for the clinical significance of any anti-donor antibody.
  • Women of childbearing potential who currently are pregnant (HCG+) or who are not practicing adequate contraception or who are breastfeeding
  • Uncontrolled viral, bacterial, or fungal infections (currently taking medication and ha
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02120157). 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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