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临床试验/NCT04822766
NCT04822766进行中(未招募)不适用

Allogeneic Hematopoietic Cell Transplantation Versus Best Available Standard of Care Therapy in Elderly Patients With Acute Myeloid Leukemia: a Randomized Phase 3 Trial

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年12月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
24
试验地点
1
主要终点
Overall survival

研究概览

简要总结

A subject of major interest for researchers, clinicians, patients, and payers, is the role of allogeneic hematopoietic stem cell transplantation (allo-HSCT) in the treatment of these older patients with AML. With conventional induction chemotherapy or hypomethylating agents, the expected 2-year overall survival (OS) is less than 25% in patients with intermediate- or high-risk disease. The 2-year OS ranges from 50 to 56% with allo-HSCT in AML patients older than 65 years.

Performing an allo-HSCT in older patients is however still controversial because of the higher risk of non-relapse mortality (15 to 35%) and graft-versus-host disease. Depending on the center policy, patients older than 65 years will either be contraindicated for transplant or will receive allo-HSCT.

With a phase III comparative, randomized, controlled, prospective, multicenter study, the trial aim to assess prospectively the outcomes and quality of life of older patients with AML receiving allo-HSCT strategy compared to those receiving a non-transplant approach.

详细描述

Every year, 30,000 patients in Europe and 20,000 in the USA are diagnosed with acute myeloid leukemia (AML). More than half of them are over 65 years old. In this older population, the median overall survival (OS) is only 2 to 8 months. With conventional induction chemotherapy or hypomethylating agents, the expected 2-year OS is less than 25% in patients with intermediate- or high-risk disease.

Performing an allo-HSCT in older patients is however still controversial because of the higher risk of non-relapse mortality (15 to 35%) and graft-versus-host disease. Depending on the center policy, patients older than 65 years will either be contraindicated for transplant or will receive allo-HSCT. Noteworthy, no prospective randomized trial has yet compared allo-HSCT to a non-transplant strategy in older patients with AML. A previous attempt made 10 years ago, by the EBMT to run a slightly similar trial, has failed in France and most European countries, mainly (i) because it mandated the type of transplant procedure to be applied and (ii) because of the absence of novel and effective drugs.

Every year, 30,000 patients in Europe and 20,000 in the USA are diagnosed with acute myeloid leukemia (AML). More than half of them are over 65 years old. In this older population, the median overall survival (OS) is only 2 to 8 months. With conventional induction chemotherapy or hypometylating agents, the expected 2-year OS is less than 25% in patients with intermediate- or high-risk disease.

Performing an allo-HSCT in older patients is however still controversial because of the higher risk of non-relapse mortality (15 to 35%) and graft-versus-host disease. Depending on the center policy, patients older than 65 years will either be contraindicated for transplant or will receive allo-HSCT. Noteworthy, no prospective randomized trial has yet compared allo-HSCT to a non-transplant strategy in older patients with AML. A previous attempt made 10 years ago, by the EBMT to run a slightly similar trial, has failed in France and most European countries, mainly (i) because it mandated the type of transplant procedure to be applied and (ii) because of the absence of novel and effective drugs.

New targeted therapies and treatment strategies are evolving rapidly. A standardized unique treatment administrated to all sub-types of AML is no longer the optimal approach for induction and non-transplant maintenance strategies. No treatment has reached consensus for older patients. For these reasons, this trial will not limit the choices of drugs administered to the patients but compare two strategies allowing patients to receive the best available standard of care.

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
65 Years 至 75 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women
  • Age ≥ 65 and ≤ 75 years
  • Newly diagnosed patients with de novo or secondary AML in first complete remission who are considered as potential candidates and eligible for an allo-HSCT procedure
  • Presence of a donor (matched related or unrelated or haplo-mismatched) willing to donate peripheral blood stem cells
  • Patient is fit for the allo-HSCT procedure
  • Patient is fit for further consolidation therapy (non-transplant arm)
  • Written informed consent

排除标准

  • Acute promyelocytic leukemia (AML FAB M3)
  • AML deemed not eligible for allo-HSCT
  • Karnofsky score <70%
  • HIV positive patient
  • Life expectancy less than one month according to the attending physician
  • Acute or chronic heart failure (Cardiac ejection fraction < 40%)
  • Pulmonary function - diffusion capacity < 50% predicted
  • Estimated glomerular filtration rate < 50 ml/min (CKD-EPI)
  • Severe neurological disorders
  • Patient subject to a legal protection measure (guardianship, curatorship and safeguard of justice) or unable to consent
  • Patient deprived of their liberty by a judicial or administrative decision
  • Patient with severe psychiatric disorders or hospitalized without consent for psychiatric care

研究组 & 干预措施

Chemotherapy

Active Comparator

干预措施: Best chemotherapy treatment (Drug)

Allogeneic Hematopoietic Cell Transplantation

Experimental

Time of transplant procedure The best available treatments of AML

干预措施: Hematopoietic stem cell transplantation (Procedure)

结局指标

主要结局

Overall survival

时间窗: 2 years after the inclusion

From inclusion (time of identification of potential donor) until death or at 24 months, whichever comes first\]

次要结局

  • Quality of life FACT-BMT(at baseline, 12 and 24 months after inclusion)
  • Quality of life EQ 5D 5L(at baseline, 12 and 24 months after inclusion)
  • Leukemia free survival(within the 2 years after inclusion)
  • The Incremental cost-effectiveness ratios (ICERs) expressed in cost per quality-adjusted life-year (QALY) gained(2 years after inclusion)
  • The Incremental cost-effectiveness ratios (ICERs) expressed in cost per Life Year Gained(2 years after inclusion)
  • In allo-HSCT patients only: cumulative incidence of acute and chronic graft-versus-host disease (GVHD)(within the 2 years after inclusion)
  • Assessment of MRD and time to relapse from inclusion up to 2 years(: time between inclusion and date of relapse or at 24 months, whichever comes first])
  • In allo-HSCT patients only: severity of acute and chronic graft-versus-host disease (GVHD)(within the 2 years after inclusion)
  • Non-relapse mortality(within the 2 years after inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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