SCID Bu/Flu/ATG Study With T Cell Depletion

Phase 1

Terminated

Conditions: Severe Combined Immunodeficiency

Interventions: Device: unrelated PBSC with T cell depletion
Biological: unrelated cord blood
Biological: unrelated BM with T cell depletion
Biological: haplo BM with T cell depletion

Registration Number: NCT02127892

Lead Sponsor: Neena Kapoor, M.D.

Brief Summary: This is a pilot clinical trial of hematopoietic stem cell transplantation for patients with a diagnosis of Severe Combined Immune Deficiency (SCID) who do not have an HLA-matched sibling donor. The stem cells will be derived from a 1) matched unrelated donor (MUD), 2) unrelated cord blood donor, or 3) a haplo-identical (parental) donor (in descending order of preference).Patients will receive a novel conditioning regimen with Busulfan, Fludarabine and Anti-thymocyte globulin (ATG) followed by an unrelated donor hematopoietic stem cell transplant (HSCT) with T-cell depletion using the CliniMACS device.

Detailed Description: The study is being conducted to assess the following:

* overall survival

* event-free survival (events are defined as: death,non-engraftment/2nd transplant, immune reconstitution failure)

* acute toxicity of the conditioning regimen

* engraftment frequency immune reconstitution frequency and tempo acute and chronic graft-versus-host disease (GVHD), frequency and severity.

The outcome from this protocol will be compared to the retrospective cohort consisting of all patients who have undergone haplo-identical HSCT for SCID at CHLA from 1984-2006 based on the assessment of the above-listed endpoints.

The CliniMACS device will be used for CD34+ selection in place of the Isolex 300i. The CliniMACS CD34 Reagent System is an investigational medical device that has not yet been approved by the FDA. This device is used in vitro to select and enrich specific cell populations. When using the CliniMACS CD34 Reagent, the system selects CD34+ cells from heterogenous hematological cell populations for transplantation in cases where this is clinically indicated.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 9

Inclusion Criteria

All patients with SCID who lack a histocompatible sibling or HLA-matched related donor will be considered as candidates for this study protocol.
Eligible patients must have adequate physical function to tolerate the chemotherapy conditioning regimen and the HSCT, as measure by:
1. Renal: creatinine clearance or GFR ≥50 ml/min/1.73m2, and not requiring dialysis
2. Pulmonary: Because patients with SCID frequently present with infectious pneumonia causing ventilatory failure, patients will be considered for enrollment in the study even if respiratory failure requiring mechanical ventilatory support is present. In patients recently diagnosed with pneumonia, efforts to stabilize the respiratory status will be made prior to enrollment in the study.
3. Infectious disease status. The presence of infection per se will not be a reason for exclusion from the study. Patients with SCID are frequently infected with both routine pathogens as well as opportunistic infections. Antibiotic, antifungal and antiviral prophylaxis and therapy will be instituted as clinically indicated. Despite the use of antimicrobial therapy, the ability to control infections will not be achieved unless HSCT is performed. Therefore, subjects may be enrolled in the study, even though infection is present, because control of infection may depend on engraftment of a donor immune system.
4. Patients will be 0-21 years of age.

Exclusion Criteria

Patient with histocompatible sibling or other related donor
End-organ failure that precludes the ability to tolerate the transplant procedure, including conditioning.
Renal failure requiring dialysis
Congenital heart disease resulting in congestive heart failure
Severe CNS disease, e.g., coma or intractable seizures
Ventilatory failure due to non-infectious etiology
Major congenital anomalies that adversely affect survival, eg CNS malformations
Metabolic diseases that would affect transplant survival, eg urea cycle disorders
HIV infection

Since the only chance of survival for patients with SCID is successful transplantation, all patients with SCID will be considered to be potential subjects for the study, regardless of end-organ dysfunction.

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
unrelated PBSC with T cell depletion	unrelated PBSC with T cell depletion	The preferred source will be bone marrow, however, if a donor is unable or unwilling to donate bone marrow, peripheral blood stem cells (PBSC) will be allowed.
unrelated cord blood	unrelated cord blood	Acceptable matching for unrelated cord blood will be a genotypic match at 6 of 6 alleles (HLA A, B and DR) or 5 of 6 alleles, but not with mismatches at both alleles of a single locus (e.g. not mismatched for both HLA A alleles).
unrelated BM with T cell depletion	unrelated BM with T cell depletion	Acceptable matching for matched unrelated donor (MUD) bone marrow will be genotypic matches at 10 of 10 HLA alleles (HLA-A, B, C, DR and DQ) or 9 of 10 HLA alleles.
haplo BM with T cell depletion	haplo BM with T cell depletion	If there is no unrelated donor available meeting the matching criteria for unrelated bone marrow or unrelated cord blood donors.

Primary Outcome Measures

Name	Time	Method
Number of Participants With Engraftment	100 day	Engraftment is defined as recovery of blood counts (neutrophil and platelet engraftment) with cells of donor origin, documented by either bone marrow or peripheral blood chimerism assays after hematopoietic stem cell transplant.

Secondary Outcome Measures

Name	Time	Method
Number of Participants With Donor-derived CD3+ T Lymphocytes >/= 100/mm3	1 year	Absolute number of donor-derived CD3+ T lymphocytes \>/= 100/mm3 in participating subjects.