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临床试验/NCT02130869
NCT02130869已完成1 期

A Pilot Study of Immunotherapy Including Haploidentical NK Cell Infusion Following CD133+ Positively-Selected Autologous Hematopoietic Stem Cells in Children With High Risk Solid Tumors or Lymphomas

St. Jude Children's Research Hospital1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2014年10月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
8
试验地点
1
主要终点
Percent of participants with positive ANC engraftment

研究概览

简要总结

This is a pilot clinical trial investigating the addition of haploidentical natural killer cell infusion to autologous stem cell transplantation. This intervention will be evaluated in children with high-risk solid tumors for whom autologous transplantation is indicated. Natural killer cells from a haploidentical family member will be given after high dose chemotherapy and positively selected autologous stem cells. In patients with neuroblastoma, the anti-GD2 antibody hu14.18K322A will also be given. The effect on normal hematopoietic cell recovery will be evaluated and survival of children treated with this approach will be determined.

The investigators expect to enroll 36 participants. Haploidentical family members (donors) will also be recruited to provide natural killer cells.

详细描述

Primary Objective:

  • To evaluate day +35 ANC engraftment in autologous stem cell transplantation for high risk pediatric malignancies after stem cell selection and immunotherapy.

Secondary Objectives

  • To estimate incidence of relapse, disease-free survival and overall survival.
  • To characterize lymphocyte and hematopoietic reconstitution in these patients.
  • To describe the characteristics of the stem cell and natural killer cell grafts.
  • To estimate the overall survival of patients treated without stem cell manipulation or NK cell infusion due to off therapy criteria

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CD133+ selected autologous stem cell infusion (Biological)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: IL-2 (Biological)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: hu14.18K322A (Biological)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Busulfan (Drug)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Melphalan (Drug)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: GM-CSF (Biological)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Haploidentical natural killer cell infusion (Device)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: G-CSF (Biological)

Group A: Neuroblastoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group A participants receive busulfan, melphalan, CD133+ selected autologous stem cell infusion, hu14.18K322A, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CliniMACS (Device)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CD133+ selected autologous stem cell infusion (Biological)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: IL-2 (Biological)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Melphalan (Drug)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: GM-CSF (Biological)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Bendamustine (Drug)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Etoposide (Drug)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Cytarabine (Drug)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Haploidentical natural killer cell infusion (Device)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: G-CSF (Biological)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Etoposide phosphate (Drug)

Group B: Lymphoma

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group B participants receive bendamustine, etoposide (or etoposide phosphate), cytarabine, melphalan, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CliniMACS (Device)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CD133+ selected autologous stem cell infusion (Biological)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: IL-2 (Biological)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Melphalan (Drug)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: GM-CSF (Biological)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Etoposide (Drug)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Carboplatin (Drug)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Haploidentical natural killer cell infusion (Device)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: G-CSF (Biological)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: Etoposide phosphate (Drug)

Group C: High-Risk Tumors

Experimental

All participants first receive standard of care high-dose chemotherapy specific to their tumor type. Group C participants receive melphalan, etoposide (or etoposide phosphate), carboplatin, CD133+ selected autologous stem cell infusion, IL-2, haploidentical natural killer cell infusion, G-CSF, and GM-CSF.

Cells for infusion are prepared using the CliniMACS System.

干预措施: CliniMACS (Device)

结局指标

主要结局

Percent of participants with positive ANC engraftment

时间窗: Day 35 post transplant

Feasibility will be determined based on ANC engraftment defined as ANC ≥500/mm\^3 for 3 consecutive tests performed on different days evaluated before day 35 post-transplant. If the study is considered feasible, the ANC engraftment rate will be 100% (95% Blyth-Still-Casella (BSC) CI: 76.45%-100%) without any failure, 92% (BSC 95% CI: 65.11%-99.57%) with 1 failure, and 83% (BSC 95% CI: 55%-96.95%) with 2 failures. In addition, if more than 2 (≥ 3) on-therapy patients die due to any protocol treatment-related causes during the first 12 months post-transplant across all groups (3 deaths among 36 participants), the study will be stopped. Deaths due to treatment not specified in this protocol will not be included in evaluation of this stopping rule.

次要结局

  • Overall survival(Up to one year after transplantation)
  • Disease-free survival(Up to one year after transplantation)
  • Lymphocyte and hematopoietic reconstitution(Up to one year after transplantation)
  • Characteristics of the stem cell grafts(Up to one year after transplantation)
  • Characteristics of the natural killer cell grafts.(Up to one year after transplantation)
  • Overall survival of patients treated without stem cell manipulation or NK cell infusion due to off therapy criteria(Up to one year after transplantation)
  • Incidence of relapse(Up to one year after transplantation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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