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临床试验/NCT02395822
NCT02395822已完成2 期

MT2014-25: Haploidentical Donor Natural Killer (NK) Cell Infusion With Subcutaneous Recombinant Human IL-15 (rhIL-15) in Adults With Refractory or Relapsed Acute Myelogenous Leukemia (AML)

Masonic Cancer Center, University of Minnesota1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2015年10月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
17
试验地点
1
主要终点
< 5% Marrow Blast, no Circulating Peripheral Blasts and Neutrophil Count of > 1 x 10^9/L

研究概览

简要总结

A phase II trial of CD3/CD19 depleted, IL-15 activated, donor natural killer (NK) cells in adults and subcutaneous IL-15 given after a preparative regimen for the treatment of relapsed or refractory acute myelogenous leukemia (AML). The primary objective is to study the potential efficacy of NK cells and IL-15 to achieve complete remission while maintaining safety.

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

入选标准

  • •(Recipient):
  • •Meets ONE of the following disease criteria:
  • •Primary AML induction failure: no CR after 2 or more induction attempts
  • •Relapsed AML or Secondary AML (from MDS or treatment related): not in CR after 1 or more cycles of standard re-induction therapy
  • •AML relapsed > 2 months after transplant: No re-induction required, and no more than 1 re-induction cycle is allowed.
  • •Relapsed AML for patients > 60 years of age the 1 cycle of standard chemotherapy is not required if either of the following criteria is met:
  • •Relapse within 6 months of last chemotherapy
  • •BM blast count < 30% within 10 days of starting protocol therapy
  • •Available related HLA-haploidentical donor (aged 14 to 75 years) by at least Class I serologic typing at the A&B locus
  • •Karnofsky Performance Status ≥ 60%
  • •Patients must have adequate organ within 14 days (28 days for pulmonary and cardiac) of study registration
  • •Able to be off prednisone or other immunosuppressive medications for at least 3 days prior to NK cell infusion (excluding preparative regimen pre-medications).
  • •Agrees to use contraception prior to study entry and for the duration of study participation.

排除标准

  • •(Recipient):
  • •Bi-phenotypic acute leukemia.
  • •Transplant < 60 days prior to study enrollment.
  • •Active autoimmune disease.
  • •History of severe asthma
  • •Uncontrolled intercurrent illness
  • •New or progressive pulmonary infiltrates on screening chest x-ray or chest CT scan that has not been evaluated with bronchoscopy
  • •Pleural effusion large enough to be detectable on chest x-ray.
  • •Pregnant women
  • •History of HIV, active or chronic hepatitis B, hepatitis C or HTLV-I infection
  • •Known hypersensitivity to any of the study agents used
  • •Received investigational drugs within the 14 days of study registration.
  • •Known active CNS involvement.
  • •Criteria For Initial Donor Selection:
  • •Related donors (sibling, parent, offspring, parent or offspring of an HLA identical sibling).
  • •14-75 years of age.
  • •At least 40 kilogram body weight.
  • •In general good health as determined by the evaluating medical provider.
  • •HLA-haploidentical donor/recipient match by at least Class I serologic typing at the A&B locus.
  • •Not pregnant.
  • •Able and willing to undergo apheresis.

研究组 & 干预措施

Preparative Regimen and SubQ rHuIL-15

Experimental

Preparative Regimen of Fludarabine and Cyclophosphamide

IL-15 Activation of Donor NK Cells:

IL-15 to Facilitate NK Cell Survival and Expansion

干预措施: IL-15 (Biological)

结局指标

主要结局

< 5% Marrow Blast, no Circulating Peripheral Blasts and Neutrophil Count of > 1 x 10^9/L

时间窗: Day 42 post NK cell infusion

Without platelet recovery

次要结局

  • In Vivo Expansion (>100) of NK Cells (Defined at CD56+/CD3- Lymphocytes)(Day 14 post NK cell infusion)
  • Proportion of Patients Experiencing Grade, 3, 4, and 5 Toxicities (Assessed by CTCAE v. 4)(Days 1-5 and Days 8-12, 24 hours after the last IL-15 dose, Day +28, Day +42)
  • Treatment Related Mortality(6 months post-therapy)
  • Number of Subjects Achieving Complete Response, Defined as in Vivo Donor Derived NK Cell Expansion of > 100 Donor Derived NK Cells.(Day 42 post NK cell infusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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