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临床试验/NCT00996359
NCT00996359终止1 期

Partially HLA-Matched Irradiated Allogeneic Cellular Therapy After Reduced Intensity Total Body Irradiation

University of Medicine and Dentistry of New Jersey2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2009年10月最近更新:
适应症

试验速览

阶段
1 期
状态
终止
入组人数
4
试验地点
2
主要终点
Toxicity

研究概览

简要总结

RATIONALE: Giving low-dose total-body irradiation before a donor stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect).

PURPOSE: This phase I trial is studying the side effects of donor stem cell transplant after total-body irradiation and to see how well it works in treating patients with relapsed or refractory hematologic cancer or acute myeloid leukemia or acute lymphocytic leukemia in complete remission.

详细描述

OBJECTIVES:

Primary

  • To evaluate the toxicity of irradiated haploidentical allogeneic cellular therapy after low-dose total-body irradiation and no pharmacologic graft-vs-host disease prophylaxis in patients with relapsed or refractory hematologic malignancies or patients with acute myeloid leukemia (AML) or acute lymphoblastic leukemia in second or greater complete remission (CR2).

Secondary

  • To evaluate immunologic parameters before and after haploidentical therapy.
  • To demonstrate host anti-leukemia T-cells in a subset of patients with AML who are HLA-A2-positive.
  • To observe any evidence of antitumor activity within the confines of this pilot study and/or assess the duration of remission in those patients who enter the study in CR2.

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

年龄范围
13 Years 至 —(Child, Adult, Older 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

结局指标

主要结局

Toxicity

时间窗: 3 years

次要结局

  • Immunologic parameters before and after haploidentical therapy(3 years)
  • Anti-tumor activity and/or duration of remission in those patients who enter the study in second complete remission or greater(3 years)
  • Treatment-related mortality(3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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