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Mismatched Donor Cells to Treat Acute Myeloid Leukemia (ATAC-AML-01)

2017年8月28日 更新者:Elizabeth Krakow、Maisonneuve-Rosemont Hospital

Adoptive Transfer of Alloreactive Cells to Treat Patients With Poor-Prognosis Acute Myeloid Leukemia-01

The purpose of this study is to assess the safety and efficacy of infusing immune cells from a donor as treatment for patients with acute myeloid leukemia that is resistant to chemotherapy or who have experienced relapse. Unlike standard bone marrow or stem cell transplantation which uses donors who are well 'matched' to the patient, this study uses donors whose immune cells are not compatible with the patient. With standard stem cell or bone marrow transplantation, the well-matched immune cells will attack the leukemia but they also attack the patient's organs (a situation called graft-versus-host disease, which can persist in the long term). Our hypothesis is that the mismatched donor cells will fight the leukemia but will then be eliminated from the patient's body, so long-term side effects like graft-versus-host disease should not occur.

研究概览

地位

未知

详细说明

The ATAC cell therapy product contains unselected, non-mobilized peripheral blood mononuclear cells from related donors who are mismatched to the recipients at 3 or more (out of 6) HLA loci. Cohorts of 3 patients will be treated at each of four pre-specified dose levels (T cells per kg recipient weight). One ATAC infusion is administered 24-48 hours following re-induction chemotherapy (for relapsed or primary refractory AML patients not in remission). In situations where ATAC infusion is not available immediately following re-induction chemotherapy and patients nonetheless achieve complete remission, one ATAC infusion is given 24-48 hours after consolidation chemotherapy.

研究类型

介入性

注册 (预期的)

12

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Quebec
      • Montreal、Quebec、加拿大、H1T 3M4
        • 招聘中
        • Hopital Maisonneuve-Rosemont

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Recipient Inclusion Criteria:

  • Age ≥ 18 years (no upper age limit, but physician discretion is advised)
  • AML that is refractory to 2 courses of induction therapy (that together constitute the 'first-line' therapy) or that has relapsed after a period of morphologic complete remission or morphologic remission with incomplete blood count recovery (CRi)
  • Candidacy for intense induction chemotherapy (ECOG 0-2, adequate renal, liver and cardiac function, absence of uncontrolled infections)
  • Availability of parents, siblings or children who are HLA haploidentical (and not homozygous for the shared haplotype), who are deemed suitable donors after medical evaluation, and who complete peripheral blood mononuclear cell collection
  • No history of autologous or allogeneic stem cell transplant, purine analog chemotherapy or cyclophosphamide, or total body irradiation
  • Ability to comprehend the investigational nature of the study and provide informed consent

Recipient Exclusion Criteria:

  • Acute promyelocytic leukemia (including those with non-classical rearrangements of RARα)
  • History of severe myelodysplastic syndrome clearly preceding the diagnosis of AML (i.e., red cell transfusion dependence or erythropoietin dependence over a 4-month period, or in the absence of a clear cause, any of the following: hemoglobin consistently below 9 g/dL or platelets below 50 x 10^9/L or ANC below 1000/uL on 2 or more occasions 2 weeks apart, or use of G-CSF to maintain the ANC threshold in the absence of infection, in the 3 months preceding the diagnosis of AML). Exception: If ATAC therapy is being considered as a bridge to stem cell transplantation in patients with an available standard transplant donor (familial, unrelated, or cord blood), this exclusion criterion does not apply.
  • Grade 2-3/3 fibrosis in the diagnostic bone marrow biopsy
  • DLCO < 40% predicted
  • Left ventricular ejection fraction < 40% (evaluated by ECHO or MUGA)
  • AST/SGOT > 2.5 x ULN
  • Bilirubin > 1.5 x ULN
  • Creatinine > 1.5 x ULN
  • Creatinine clearance < 50 mL/min
  • HIV positive
  • Major anticipated illness or organ failure incompatible with survival from chemotherapy
  • Concurrent second primary cancer or a prior malignancy that required cytotoxic treatment within the past 12 months, other than cervical carcinoma in-situ or prostate cancer in-situ
  • Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the treatment unlikely and informed consent impossible
  • Any congenital or acquired immunodeficiency that would possibly permit permanent engraftment of donor cells
  • Receiving systemic steroid therapy or systemic immunosuppression such as cyclosporine or TNF-inhibitors
  • Prior or concurrent receipt of any marketed or investigational agent deemed on an ad hoc basis to cause immunomodulation, pose a threat of permanent engraftment or increase the risk of GVHD.

Donor inclusion criteria:

  • Mismatched family donor (incompatibility at 3 loci HLA-A, B and DR of the unshared haplotype, or higher-order incompatibility)
  • Age ≥ 16 and ≤ 80 years
  • Fit to undergo apheresis (normal blood counts, normotensive and no history of stroke).
  • Donor has been tested negative for HIV-1, HIV-2, hepatitis B virus (HBV, surface and core antigen), hepatitis C virus, human T-lymphotropic virus types I/II, and Treponema pallidum (syphilis).
  • ECOG performance status of 2 or less.
  • Adequate veins for leukapheresis or agree to placement of a temporary central venous catheter.
  • Donor must provide written informed consent.
  • Where multiple equally-suitable donors are available, sex mismatched donors will be preferred.

Donor exclusion criteria:

  • Medically uncontrolled coronary heart disease
  • Myocardial infarction within the last 3 months
  • History of seizure
  • History of stroke
  • History of malignancy (except basal cell or squamous carcinoma of the skin, or positive PAP smear and subsequent negative follow-up)
  • Presence of a transmissible disease (such as HIV seropositivity)
  • Presence of a major illness or a suspected systemic dysfunction
  • Presence of an an active inflammatory or autoimmune disorder
  • Female donors who are pregnant or nursing

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:ATAC Therapy
Unselected peripheral blood mononuclear cells given 24-48 hours after induction or consolidation chemotherapy
其他名称:
  • Unselected Peripheral Blood Mononuclear Cells

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Safety
大体时间:60 days (up to 2 years)
Maximum tolerated cell dose: Dose at which < 33% of patients experienced dose-limiting toxicity. If no DLT occurs, then dose titration will stop at a pre-specified number of T cells/kg. Four dose-level cohorts are planned.
60 days (up to 2 years)

次要结果测量

结果测量
大体时间
Treatment-related mortality
大体时间:Continuous up to 2 years
Continuous up to 2 years
Non-relapse mortality
大体时间:Continuous up to 2 years
Continuous up to 2 years
Incidence of graft-versus-host disease
大体时间:Continuous up to 2 years
Continuous up to 2 years
Duration of cytopenias
大体时间:Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
Overall survival
大体时间:Continuous up to 2 years
Continuous up to 2 years
Complete and incomplete remissions (CR, CRi)
大体时间:Day 60 post cell infusion
Day 60 post cell infusion
Relapse-free survival
大体时间:Continuous up to 2 years
Continuous up to 2 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Jean-Sébastien Delisle, MD,PhD、Hôpital Maisonneuve-Rosemont and Université de Montréal
  • 首席研究员:Elizabeth Krakow, MD、Hôpital Maisonneuve-Rosemont and Université de Montréal

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年9月1日

初级完成 (预期的)

2018年12月1日

研究完成 (预期的)

2018年12月1日

研究注册日期

首次提交

2013年2月10日

首先提交符合 QC 标准的

2013年2月13日

首次发布 (估计)

2013年2月15日

研究记录更新

最后更新发布 (实际的)

2017年8月30日

上次提交的符合 QC 标准的更新

2017年8月28日

最后验证

2017年8月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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