Naive T Cell Depletion for Preventing Chronic Graft-versus-Host Disease in Children and Young Adults With Blood Cancers Undergoing Donor Stem Cell Transplant

Complete Title: RCI BMT 16-NTCD/PBMTC GVH1701: Multi-center Phase II Randomized Controlled Trial of Naïve T Cell Depletion for Prevention of Chronic Graft-Versus-Host Disease in Children and Young Adults
Trial Phase: II
Investigator: Marie Bleakley

This phase II trial studies how well naive T-cell depletion works in preventing chronic graft-versus-host disease in children and young adults with blood cancers undergoing donor stem cell transplant. This study is comparing naïve T-cell depletion transplantation to the traditional stem cell transplantation. In these transplants, chemotherapy and total-body radiotherapy ('conditioning') are used to kill residual leukemia cells and the patient's normal blood cells, especially immune cells that could reject the donor cells. Following the chemo/radiotherapy, blood stem cells from the donor are infused. These stem cells will grow and eventually replace the patient's original blood system, including red cells that carry oxygen to our tissues, platelets that stop bleeding from damaged vessels, and multiple types of immune-system white blood cells that fight infections. Mature donor immune cells, especially a type of immune cell called T lymphocytes (or T cells) are transferred along with these blood-forming stem cells. T cells are a major part of the curative power of transplantation because they can attack leukemia cells that have survived the chemo/radiation therapy and also help to fight infections after transplantation. However, donor T cells can also attack a patient's healthy tissues in an often-dangerous condition known as Graft-Versus-Host-Disease (GVHD). Drugs that suppress immune cells are used to decrease the severity of GVHD; however, they are incompletely effective and prolonged immunosuppression used to prevent and treat GVHD significantly increases the risk of serious infections. Removing all donor T cells from the transplant graft can prevent GVHD, but doing so also profoundly delays infection-fighting immune reconstitution and eliminates the possibility that donor immune cells will kill residual leukemia cells. Work in animal models found that depleting a type of T cell, called naïve T cells or T cells that have never responded to an infection, can diminish GVHD while at least in part preserving some of the benefits of donor T cells including resistance to infection and the ability to kill leukemia cells. This clinical trial studies how well the selective removal of naïve T cells works in preventing GVHD after peripheral blood stem cell transplants compared to the subjects that receive unmanipulated bone marrow transplants.

Keywords:
  • Leukemia, Acute Lymphoblastic (ALL)
  • Leukemia, Acute Myeloid (AML)
  • Myelodysplastic Syndromes (MDS)
  • Graft Versus Host Disease (GVHD)
  • Hematopoietic Stem Cell Transplantation, Allogeneic
  • Bone Marrow Diseases
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Leukemia, Acute Biphenotypic
  • Hematologic Diseases
Disclaimer: We update this information regularly. However, what you read today may not be completely up to date.
Checklist icon

Join a Clinical Trial

Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each clinical trial.

Contact Us

If you are seeking to schedule an appointment, we are here to help. You can either call us or fill out our online appointment request form.

Adult
Pediatric
II
Marie Bleakley
9880A
NCT03779854
RCI BMT 16-NTCD/PBMTC GVH1701: Multi-center Phase II Randomized Controlled Trial of Naïve T Cell Depletion for Prevention of Chronic Graft-Versus-Host Disease in Children and Young Adults
Leukemia, Acute Lymphoblastic (ALL)
Leukemia, Acute Myeloid (AML)
Myelodysplastic Syndromes (MDS)
Graft Versus Host Disease (GVHD)
Hematopoietic Stem Cell Transplantation, Allogeneic
Bone Marrow Diseases
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Acute Biphenotypic
Hematologic Diseases