Total-Body Irradiation Followed By Cyclosporine and Mycophenolate Mofetil in Treating Patients With Severe Combined Immunodeficiency Undergoing Donor Bone Marrow Transplant

Completed · Phase 1

Conditions studied: Adenosine Deaminase Deficiency, Autosomal Recessive Disorder, Immune System Disorder, Purine-Nucleoside Phosphorylase Deficiency, Severe Combined Immunodeficiency, Severe Combined Immunodeficiency With Absence of T and B Cells, X-Linked Severe Combined Immunodeficiency

In brief

This pilot clinical trial studies total-body irradiation followed by cyclosporine and mycophenolate mofetil in treating patients with severe combined immunodeficiency (SCID) undergoing donor bone marrow transplant. Giving total-body irradiation (TBI) before a donor bone marrow transplant using stem cells that closely match the patient's stem cells, helps stop the growth of abnormal cells. It may also stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may mix with the patient's immune cells and help destroy any remaining abnormal cells. Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after the transplant may stop this from happening.

Key facts

Study ID

NCT00008450

Run by

Fred Hutchinson Cancer Center

People needed

6

Starts

1997-08-11

Expected to finish

2018-12-26

Last updated by the study team

2019-07-29

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with severe combined immunodeficiency syndrome:
• SCID with presence of B lymphocytes
• X-linked SCID (presence of B lymphocytes)
• Autosomal recessive SCID
• Patients with severe combined immunodeficiency syndrome:
• SCID with absence of T and B lymphocytes
• Patients with severe combined immunodeficiency syndrome:
• Purine metabolite deficiencies, deficiencies of the purine metabolites
• Adenosine deaminase (ADA) deficiency
• Purine nucleoside phosphorylase (PNP) deficiency
• DONOR: Related donor who is human leukocyte antigen (HLA) genotypically identical at least at one haplotype and may be genotypically or phenotypically identical for serological typing for HLA-A, B, C, and at the allele level for DRB1 and DQB1; related donors other than siblings must be matched at HLA-A, B, and C (at highest resolution available at the time of donor selection) and at DRB1 and DQB1 by deoxyribonucleic acid (DNA) typing; if more than one HLA-identical sibling is available, priority will be given to the oldest normal donor
• DONOR: Unrelated donors who are prospectively matched for HLA-A, B, C, DRB1 and DQB1 by DNA typing at the highest resolution routinely available at the time of donor selection; only a single allele disparity will be allowed for HLA-A, B, or C as defined by high resolution typing

You may not qualify if…

• Patients with viral associated T cell immunodeficiency disorders, such as human immunodeficiency virus (HIV)
• Patients with other disease or organ dysfunction that would limit survival to less than 30 days
• DONOR: Identical twin
• DONOR: Pregnancy
• DONOR: HIV seropositive
• DONOR: A positive anti-donor cytotoxic cross match is absolute donor exclusion
• DONOR: Patient and donor pairs homozygous at a mismatched allele in the graft rejection vector are considered a two-HLA allele mismatch, i.e., the patient is A*0201, and this type of mismatch is not allowed
• DONOR: < 6 months old, > 75 years old

Where it is running

• Fred Hutch/University of Washington Cancer Consortium — Seattle, Washington, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.