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临床试验/NCT03597321
NCT03597321进行中(未招募)2 期

Comparative Phase II Trial of Early Prophylactic Donor Lymphocyte Infusion After Allogeneic Hematopoietic Stem Cell Transplantation for Patients With Acute Myeloid Leukemia

Institut Paoli-Calmettes1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2020年9月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
124
试验地点
1
主要终点
Relapse-free survival (RFS) at 2 years after randomization

研究概览

简要总结

Allogeneic hematopoietic stem cell transplantation (Allo-HSCT) is a curative option for patients with acute myeloid leukemia (AML). However, transplantation related toxicity and mortality as well as the existence of HLA identical sibling donor represent major limitations. Over the 20 past years, the development of reduced intensity conditioning (RIC) regimen and the use of alternative donors allowed extending the possibility of Allo-HSCT for AML, with decreased toxicity and mortality. This invited to propose this strategy to more advanced patients, making that AML recurrence has become one of the main issues after Allo-HSCT. Thus, to develop prophylactic and preemptive strategies to minimize disease recurrence after Allo-HSCT is now the main challenge in the field. Among cellular and/or pharmacological treatments after Allo-HSCT, donor lymphocyte infusion (DLI) is probably one of the most commonly used treatments after Allo-HSCT. Indeed, DLI were reported as a potential efficient immunotherapy more than 20 years ago for the treatment of patients with leukemia relapsing after Allo-HSCT. However, most of experiences were reported in the setting of relapse after Allo-HSCT and no prospective evaluation of prophylactic DLI is available so far. Thus no strong recommendation for the use of DLI after Allo-HSCT can be made. Our study proposal would like to assess the question of prophylactic DLI efficacy, as a proof of concept of early immune intervention after Allo-HSCT. The investigators, therefore, designed a prospective multicenter randomized trial evaluating the impact of early DLI on outcome after Allo-HSCT for AML.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

入选标准

  • AML in hematological complete remission at the time of inclusion
  • Patient age from 18 to
  • Able to comply with the protocol.
  • Written informed consent.
  • Allogeneic stem cell transplantation from any donor except cord blood.
  • Unmanipulated bone marrow or peripheral blood stem cells as graft source are allowed
  • Ongoing GVHD prophylaxis using cyclosporin A at the time of inclusion.

排除标准

  • Presence or history of grade 2 to 4 acute GVHD.
  • No hematological CR of AML at the time of inclusion. CR patients positive with molecular or phenotypic minimal residual disease (MRD) can be included.
  • Pregnancy/breast feeding.
  • Patient considered socially or psychologically unable to comply with the treatment and the required medical follow-up.
  • Concomitant uncontrolled disease and/or organ dysfunction (infection, severe heart, renal, respiratory or hepatic failure...).
  • Primary or secondary graft failure.
  • Previous solid organ allogeneic transplantation.

研究组 & 干预措施

Arm A-DLI

Experimental

Patients will be planned to receive prophylactic Donor Lymphocyte Injection

干预措施: prophylactic donor lymphocyte infusion (DLI) (Biological)

结局指标

主要结局

Relapse-free survival (RFS) at 2 years after randomization

时间窗: 2 years

RElpase-free survival will be evaluated in an intent-to-treat analysis by Kaplan Meier estimate and Log Rank test. Survival will be calculated from the date of randomization

次要结局

未报告次要终点

研究者

发起方
Institut Paoli-Calmettes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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