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Eligibility
for people ages up to 22 years
Location
at Oakland, California and other locations
Dates
study started
Principal Investigator
Nahal Lalefar

Description

Summary

This is a prospective non-therapeutic study, assessing the long-term toxicity of pediatric HCT for hematologic malignancies. This study is a collaboration between the Pediatric Blood and Marrow Transplant Consortium (PBMTC), the Center for International Blood and Marrow Transplant Research (CIBMTR), the National Marrow Transplant Program (NMDP) and the Resource for Clinical Investigation in Blood and Marrow Transplantation (RCI-BMT) of the CIBMTR. The study will enroll pediatric patients who undergo myeloablative HCT for hematologic malignancies at PBMTC sites.

Details

This is a prospective non-therapeutic study, assessing the long-term toxicity of pediatric HCT for hematologic malignancies. This study is a collaboration between the Pediatric Blood and Marrow Transplant Consortium (PBMTC), the Center for International Blood and Marrow Transplant Research (CIBMTR), the National Marrow Transplant Program (NMDP) and the Resource for Clinical Investigation in Blood and Marrow Transplantation (RCI-BMT) of the CIBMTR. The study will enroll pediatric patients who undergo myeloablative HCT for hematologic malignancies at PBMTC sites.

The study examines the hypothesis that survivors of pediatric HCT are at risk for late organ toxicity and they will have identifiable biomarkers present within the first two years following HCT which will be predictive for late adverse outcomes allowing for early identification of patients at risk.

Keywords

Acute Lymphoblastic Leukemia/Lymphoma Myelodysplasia Acute Myelogenous Leukemia Juvenile Myelomonocytic Leukemia Chronic Myelogenous Leukemia

Eligibility

You can join if…

Open to people ages up to 22 years

  1. Age less than 22 years at admission for HCT
  2. Planned allogeneic HCT from any donor and stem cell source. There are no study-specific criteria for HLA-matching
  3. Disease and disease status criteria
  4. Acute lymphoblastic leukemia/lymphoma in complete morphologic remission defined as a M1 marrow (<5% blasts) with no evidence of active extramedullary disease within 30 days of the start of the conditioning regimen; OR
  5. Myelodysplasia (regardless of subtype) with less than 10% marrow blasts within 30 days of the start of the conditioning regimen; OR
  6. Acute myelogenous leukemia in complete morphologic remission defined as an M1 marrow (<5% blasts) with no evidence of extramedullary disease within 30 days of the start of the conditioning regimen; OR
  7. Juvenile myelomonocytic leukemia; OR
  8. Chronic myelogenous leukemia excluding refractory blast crisis.
  9. Planned myeloablative conditioning regimen, defined as a regimen including one of the following as a backbone agent:
  10. Busulfan ≥ 12.8 mg/kg total dose (IV or PO). PK-based dosing allowed, if the intent is total overall dose ≥ 12.8 mg/kg; OR
  11. Total Body Irradiation ≥ 1200 cGy fractionated; OR
  12. Treosulfan ≥ 30 g/m2 total dose IV
  13. Enrollment in the following NMDP research protocols:
  14. Protocol for a Research Database for Hematopoietic Cell Transplantation, Other Cellular Therapies and Marrow Toxicity Injuries
  15. Protocol for a Research Sample Repository for Allogeneic Hematopoietic Stem Cell Transplantation and Marrow Toxic Injuries
  16. Written informed consent document signed by patient if the age is greater than or equal to 18 years and the patient is developmentally able to provide consent. The informed consent document is to be signed by the parent or legal guardian if the patient's age is less than 18 years or if the patient is older than 18 years, but developmentally unable to provide consent. Assent will be obtained according to the guidelines of the patient's transplant institution.

You CAN'T join if...

  1. Prior allogeneic or autologous HCT
  2. Patients with renal disease prior to the start of HCT conditioning requiring the use of dialysis at the time of enrollment and/or GFR < 60 mL/min/1.73 m2
  3. Patients with osteopenia or osteoporosis treated with a bisphosphonate medication at any time prior to enrollment
  4. Patients with preexisting diabetes or hyperglycemia treated with insulin or oral hypoglycemic medication at the time of enrollment
  5. Patients with uncontrolled viral, bacterial, fungal or protozoal infection at the time of study enrollment
  6. Karnofsky performance score or Lansky Play-Performance Scale Score <60 at the time of study enrollment
  7. Known inherited or constitutional predisposition to cancer including, but not limited to Down Syndrome, Li-Fraumeni syndrome, Fanconi Anemia, and patients with BRCA1 and BRCA2 mutations

Locations

  • Children's Hospital of Los Angeles accepting new patients
    Los Angeles, California, 90027, United States
  • UCLA Center for Health Sciences accepting new patients
    Los Angeles, California, 90095, United States

Details

Status
accepting new patients
Start Date
Sponsor
Center for International Blood and Marrow Transplant Research
ID
NCT02338479
Lead Scientists
Nahal Lalefar
Christopher Dvorak
Study Type
Observational
Last Updated
May 1, 2017
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