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临床试验/NCT01526096
NCT01526096已完成1 期

Pilot Study T Cell Depletion in the Setting of Autologous Stem Cell Transplantation for Patients With Multiple Myeloma

University of Chicago1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2011年7月12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
30
试验地点
1
主要终点
Purity of ex vivo depleted regulatory T cells prior to autologous stem cell transplant (arm 3 only)

研究概览

简要总结

The purpose of this study is to test whether regulatory T-cell reduction is possible and safe in myeloma subjects undergoing autologous stem cell transplantation (ASCT).

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
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptomatic multiple myeloma of any subtype in any disease stage, providing that patient does not have smoldering myeloma.
  • Patient must otherwise be a candidate for ASCT as determined by treating physician.
  • No current CNS Myeloma at time of enrollment.
  • Life expectancy greater than 12 weeks.
  • Age greater than or equal to 21 and less than or equal to 70 years old.
  • EGOG performance status less than or equal to
  • No cardiac, pulmonary, hepatic, or renal contraindications for high dose chemotherapy.
  • HIV Negative.
  • No active Hepatitis B or C.
  • Patients must be able to provide written informed, consent.

排除标准

  • Pregnant or nursing women. Women of child-bearing age must be tested for pregnancy.
  • Use of systemic immunosuppressive medications, including corticosteroids, tacrolimus, mycophenolate mofetil, sirolimus or cyclosporine A.
  • Psychiatric illness which may make compliance to the clinical protocol unmanageable or which may compromise the ability of the patient to give informed consent.
  • Active autoimmune disease including but not limited to: rheumatoid arthritis inflammatory bowel disease, celiac disease, systemic lupus erythematosis, scleroderma or multiple sclerosis.

研究组 & 干预措施

Standard ASCT (Grp 1)

Active Comparator

Standard autologous stem cell transplantation (ASCT)

干预措施: Stem cell re-infusion (Procedure)

Standard ASCT (Grp 1)

Active Comparator

Standard autologous stem cell transplantation (ASCT)

干预措施: G-CSF (Drug)

Standard ASCT (Grp 1)

Active Comparator

Standard autologous stem cell transplantation (ASCT)

干预措施: Plerixafor (Drug)

Standard ASCT (Grp 1)

Active Comparator

Standard autologous stem cell transplantation (ASCT)

干预措施: Apheresis (Procedure)

Standard ASCT (Grp 1)

Active Comparator

Standard autologous stem cell transplantation (ASCT)

干预措施: Melphalan (Drug)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: G-CSF (Drug)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: Plerixafor (Drug)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: Apheresis (Procedure)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: Melphalan (Drug)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: Stem cell re-infusion (Procedure)

Depletion of T-cells after ASCT (Grp 2)

Experimental

Standard ASCT followed by treatment with basiliximab to remove certain immune cells (called regulatory T-cells or Tregs) from the blood

干预措施: Basiliximab (Drug)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: G-CSF (Drug)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: Plerixafor (Drug)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: Apheresis (Procedure)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: Melphalan (Drug)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: Stem cell re-infusion (Procedure)

Depletion of T-cells before ASCT(Grp 3)

Experimental

Blood collected for an ASCT will be processed using a special cell sorting machine (CliniMACS device) to remove Treg cells before the stem cells are infused back into the body during stem cell transplant.

干预措施: CliniMACS CD25 microbeads and cell sorter (Device)

结局指标

主要结局

Purity of ex vivo depleted regulatory T cells prior to autologous stem cell transplant (arm 3 only)

时间窗: 1-3 days

Percentage of CD4+CD25+ regulatory T cells following ex vivo depletion in arm 3 will be analyzed by flow cytometry and compared to a pre-CD25-depletion sample. The depletion of CD25+ cells among the entire CD4+ population is expected to reach 80% efficiency.

Timing and duration of regulatory T cell depletion and recovery following autologous stem cell transplant

时间窗: 180 days

Timing and duration of regulatory T cell depletion and recovery following in vivo or ex vivo (arms 2 and 3) CD25+ T cell depletion will be performed at pre-defined timepoints prior to and following autologous stem cell transplant by flow cytometry on peripheral blood samples and directly compared to the percentages of regulatory T cells (CD4+CD25+FoxP3+ or CD4+CD25+CD127-) present at the same timepoints in patients enrolled onto arm 1 in which no regulatory T cell depletion is performed.

Incidence of autologous graft-versus-host disease following in vivo or ex vivo regulatory T cell depletion

时间窗: 180 days

The indicence of autologous graft-versus-host disease, as assessed by the development of skin rash, diarrhea and/or liver function test abnormalities consistent with autologous graft-versus-host disease following CD25+ T cell depletion and autologous stem cell transplant compared with the incidence of autologous graft-versus-host disease in patients enrolled onto arm 1 in which no regulatory T cell depletion is performed.

次要结局

  • Kinetics of recovery of peripheral blood cellular elements(180 days)
  • Number of patients that experience a complete response following autologous stem cell transplant based upon the assigned study arm using International Myeloma Working Group definitions(100 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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