Allogeneic Hematopoietic Stem Cell Transplantation for Children Affected With Malignant Osteopetrosis: A Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Engraftment
研究概览
简要总结
Malignant infantile osteopetrosis (MIOP) is a rare fatal genetic disorder that is characterized by the bone's inability to regulate remodeling. The only curative therapy is hematopoietic stem cell transplantation. Stem cells provided from an HLA identical matched sibling donor is the standard of care, but not feasible for the majority of patients. In addition, due to the potentially rapid progression of this disease, the time to identify a suitable HLA matched unrelated donor is not optimal. Therefore this study is designed to test the hypothesis that children with osteopetrosis can properly engraft hematopoietic stem cells that are donated from a partially matched parental donor, or "haploidentical" stem cell donor that are processed on the investigational device, CliniMACS selection system.
详细描述
The primary objective of this trial will be answered strictly by those patients enrolled who receive a haploidentical stem cell donor graft.
Patients with a matched sibling donor will be offered participation in this clinical trial and will receive a standard myeloablative conditioning regimen followed by the infusion of an unmanipulated bone marrow graft. However, data from these transplant recipients will be reported in a descriptive manner only.
Secondary Objectives in this trial include the following:
- To describe the outcome of children with MIOP who receive hematopoietic stem cells from a matched sibling donor or a haploidentical donor utilizing a uniform approach one year from transplant
- To estimate the fraction of children with MIOP who have a genetic defect correlating to the osteopetrosis phenotype
- To assess carrier-state of the genetic mutation in parents with an affected child
- To assess carrier-state of the genetic mutation in siblings of affected children
- To estimate the effect of age at the time of hematopoietic stem cell transplantation on the overall outcome of children with MIOP
- To describe the kinetics of select cytokine expression before and after transplantation
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of malignant osteopetrosis as documented by bone marrow biopsy and radiographic imaging
- •A suitable hematopoietic stem cell donor is available
排除标准
- •Participant has the Carbonic Anhydrase II (CAII) deficiency osteopetrosis variant
- •Symptomatic cardiac disease or evidence of significant cardiac dysfunction by ECHO (shortening fraction <30%)
- •Creatinine clearance ≤ 40ml/min/1.73m^2
- •Bilirubin ≥ 3mg/dL
- •SGPT ≥ 500 U/L
- •Evidence of current severe infection which would preclude ablative chemotherapy or a successful transplantation
- •Karnofsky or Lansky score < 70 noting expected abnormalities
研究组 & 干预措施
1
干预措施: Stem Cell Transplantation (Procedure)
1
干预措施: Miltenyi Biotec CliniMACS (Device)
1
干预措施: Systemic chemotherapy and antibodies (Drug)
结局指标
主要结局
Engraftment
时间窗: 100 days post-transplant
To determine the need for blood or platelet transfusions and the presence of donor cells being present in the transplant recipient's bone marrow or peripheral blood by 100 day after transplantation for children with malignant infantile osteopetrosis who have received a haploidentical stem cell graft.
次要结局
未报告次要终点