Busulfan and Melphalan With Autologous Hematopoietic Stem Cell Support With Positively-Selected CD133+ Hematopoietic Cells for Children With High Risk Solid Tumors and Lymphomas
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- To determine the safety of the treatment plan using Busulfan and Melphalan followed by infusion of CD133+ selected hematopoietic cells in patients with high-risk malignancies.
研究概览
简要总结
Studies have provided evidence that residual microscopic malignant cells in autologous bone marrow or blood stem cell grafts can contribute to posttransplant relapse. Researchers are currently exploring different methods in an attempt to purify or "purge" the stem cell product to minimize the risk of tumor contamination.
The CD133+ antigen is a protein contained on or "expressed" on numerous cells in the human body including specific hematopoietic progenitor (blood forming) cells. However, this antigen is not expressed on certain cancer cells including neuroblastoma. A technique using the investigational CliniMACS cell sorting device has been developed in an effort to filter out only those stem cells that express this CD133+ antigen in order to infuse a hematopoietic stem cell product with no tumor contamination potential.
The primary objective of this study is to establish safety of treating patients with a high dose chemotherapy regimen of Busulfan and Melphalan followed by autologous CD133+ hematopoietic stem cell support. Transplants recipients are expected to achieve engraftment as defined by an absolute neutrophil count of greater than or equal to 500/mm3 for three consecutive days by day 42-post infusion. Thus, safety of the treatment plan will be evaluated in terms of failure to engraft by this specific time period.
详细描述
Secondary objectives for this protocol include the following:
- To describe CD133+ graft content post-selection and to describe the yield and purity of CD133+ content of the graft obtained.
- To describe the negative selection efficiency of this strategy by assessing the processed product for tumor specific markers, when applicable.
- To characterize the proliferation of clonal progeny of CD133+ cells.
- To characterize lymphocyte and hematopoietic reconstitution (including the kinetics of platelet engraftment) in these patients.
- To estimate one-year disease-free and overall survival in these transplant recipients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- — 至 25 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Eligibility will be determined separately for Part I and Part II of this study:
- •Part I ( Part I Eligibility criteria (eligibility for undergoing apheresis procedure)
- •Age ≤ 25 years at initial diagnosis.
- •Must have one of the following diagnoses:
- •High risk neuroblastoma
- •Metastatic or recurrent retinoblastoma
- •High risk rain tumors
- •Recurrent or refractory Hodgkin disease
- •Recurrent or advanced stage Wilms tumor
- •Recurrent or metastatic sarcomas
- •Recurrent or refractory non-Hodgkin lymphoma
- •Desmoplastic small round cell tumor.
- •Lansky or Karnofsky Performance Score ≥
- •Creatinine ≤ 2.0 mg/dl.
- •Direct bilirubin ≤ 2.0 mg/dl.
- •SGPT ≤ 2 x upper limit of normal
- •HIV testing
- •Negative pregnancy test
- •Patients with significant prior radiation therapy to the liver will be excluded.
- •Part II eligibility criteria (criteria for transplantation of CD133 select stem cell product)
- •Successfully completed Part I of protocol treatment plan and has the following available:
- •Stored autologous bone marrow or peripheral blood stem cells (i.e. 2 x 106 unselected CD34+ cells/ kg PBSC or 1 x 106 CD34+ cells/ kg BM) for back up.
- •Stored autologous bone marrow or peripheral blood stem cells (2 x 106 CD133+ cells/ kg PBSC or 2 x 106 CD133+ cells/ kg BM) for infusion.
- •Forced vital capacity greater than or equal to 40% normal or pulse oximetry greater than or equal to 92% on room air.
- •Lansky or Karnofsky Performance Score ≥
- •Creatinine ≤ 2.0 mg/dl.
- •Direct bilirubin ≤ 2.0 mg/dl.
- •SGPT ≤ 2 x upper limit of normal
- •Negative pregnancy test
- •Patients with significant prior radiation therapy (in opinion of the PI) to the liver will be excluded.
排除标准
- 未提供
研究组 & 干预措施
1
干预措施: Stem Cell Transplantation (Procedure)
1
干预措施: Busulfan, Melphalan (Drug)
结局指标
主要结局
To determine the safety of the treatment plan using Busulfan and Melphalan followed by infusion of CD133+ selected hematopoietic cells in patients with high-risk malignancies.
时间窗: August 2005
次要结局
未报告次要终点