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临床试验/NCT00675831
NCT00675831已完成1 期

Infusion of Donor Lymphocytes Depleted of CD25+ Regulatory T-cells in Patients With Relapsed Hematologic Malignancies After Matched Allogeneic Hematopoietic Stem Cell Transplantation

Dana-Farber Cancer Institute1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2007年12月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
24
试验地点
1
主要终点
To determine the feasibility of using the ClinMACS CD25 Reagent device to engineer a DLI product outlined in the protocol

研究概览

简要总结

The purpose of this research study is to evaluate the safety and efficacy of cell depletion in a donor lymphocyte infusion (DLI) product with the use of the CliniMACS machine. Previously, patients with hematologic malignancies who have relapsed after transplant have been given infusions of donor white blood cells calsed donor lymphocyte infusion (DLI) as a way to boost their immune function and fight cancer. Information from other research studies suggests that lowering the number of a certain type of white blood cell called CD25+ Tregs in the DLI may allow for a greater effect. In this research study, we are looking for the appropriate dose of DLI depleted of the CD25+ Treg white blood cells that can be given safely.

详细描述

  • The original marrow/stem cell donor will undergo one or two white blood cell collection procedures called leukopheresis. The cells collected from the first leukopheresis will be sent to the laboratory where the amount of white blood cells collected will be measured. If the number of cells collected at the first leukopheresis is not enough, the donor will have a second leukopheresis procedure.
  • Once enough lymphocytes are collected from the donor, the CliniMACS CD25 Reagent System device will reduce the number of CD25+ Tregs. The CD25+ depleted donor lymphocytes will then be infused to the participant intravenously. Participants will be observed for about one hour after the infusion.
  • One, two, four and eight weeks after the DLI, participants will return to the clinic for follow-up visits. At each visit a physical exam, questions about the participants general health, and blood tests will be performed.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with hematologic malignancies that have relapsed after HLA-A, -B, -C, and-DRBI matched allogeneic hematopoietic stem cell transplantation
  • •At least 2 months following hematopoietic stem cell transplantation
  • •Off any systemic immunosuppressive medication for treatment or prevention of GVHD, for a minimum of 2 weeks prior to study entry
  • •Recipient with donor chimerism of 20% or greater within 6 weeks prior to DLI
  • •Patient with less than 50% bone marrow involvement (% cellularity) and less than 5cm lymph nodes, in the 6 weeks prior to DLI
  • •18 years of age or older
  • •ECOG Performance Status score 0-2
  • •Prior stem cell donor is medically fit to undergo leukapheresis procedure

排除标准

  • •Relapsed CML in chronic phase
  • •Prior donor lymphocyte infusion or other immunotherapy treatment within 8 weeks prior to enrollment
  • •Chemotherapy within 4 weeks prior to enrollment
  • •Clinically significant and active autoimmune disease in donor or patient. This is defined as autoimmune disease resulting in organ dysfunction and/or requiring systemic therapy
  • •Evidence of active acute or chronic GVHD
  • •Uncontrolled infection

研究组 & 干预措施

CD25+ Treg depleted DLI dose schema

Experimental

Patients will receive a defined dose of CD25+ Treg depleted DLI. 5 patients will be enrolled, initially at dose level B, and subsequent cohorts will be dose adjusted per the CD3+ dose escalation/de-escalation schema:

  • Dose level -C: 3x10^7 (CD3+Dose (#cells/kg*))
  • Dose level -B: 1x10^7 (CD3+Dose (#cells/kg*))
  • Dose level -A: 1x10^6 (CD3+Dose (#cells/kg*)) *Recipient's body weight in Kg

干预措施: CliniMACS CD25 Reagent Device (Device)

结局指标

主要结局

To determine the feasibility of using the ClinMACS CD25 Reagent device to engineer a DLI product outlined in the protocol

时间窗: 3 years

To determine the safety of CD25+ Treg depleted DLI in this patient population.

时间窗: 3 years

次要结局

  • To assess clinical response after infusions of CD25+ Treg depleted donor lymphocytes(3 years)
  • To assess the immunologic impact of infusions of CD25+ Treg depleted donor lymphocytes(3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Koreth, MD

MBBS, DPhil

Dana-Farber Cancer Institute

研究点 (1)

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