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FLUDARABINE-TREOSULFAN REDUCED INTENSITY CONDITIONING REGIMEN PRIOR HAPLOIDENTICAL STEM CELL TRANSPLANTATION WITH POST TRANSPLANTATION CYCLOPHOSPHAMIDE FOR OLDER AND/OR FRAIL PATIENTS WITH AML (FT-RIC-HAPLO)

2026年5月19日 更新者:Institut Paoli-Calmettes

FLUDARABINE-TREOSULFAN REDUCED INTENSITY CONDITIONING REGIMEN PRIOR HAPLOIDENTICAL STEM CELL TRANSPLANTATION WITH POST TRANSPLANTATION CYCLOPHOSPHAMIDE FOR OLDER AND/OR FRAIL PATIENTS WITH AML: FT-RIC-HAPLO-IPC 2025-016

Acute myeloid leukemia (AML) and high-risk myelodysplastic syndromes (MDS) predominantly affect older adults, and their incidence continues to rise with advanced age. For many patients, allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative option capable of providing long-term disease control through the graft-versus-leukemia (GVL) effect. Historically, however, allo-HSCT was rarely offered to patients older than 50 years because of the high morbidity and mortality associated with myeloablative conditioning regimens and limited supportive care strategies. Over the past two decades, advances in reduced-intensity conditioning (RIC), infection prophylaxis, and donor availability have profoundly transformed the landscape, allowing increasing numbers of older patients to access transplantation.

Multiple studies have demonstrated that allo-HSCT confers a survival benefit in older AML patients in complete remission compared with consolidation chemotherapy alone.

The intensity of conditioning profoundly influences both relapse risk and non-relapse mortality (NRM). myeloablative conditioning (NMAC) regimens are attractive for older adults due to their low toxicity but rely solely on the immunologic GVL effect and thus carry a higher relapse risk. Reduced-intensity conditioning (RIC) regimens, incorporating intermediate-dose alkylating agents such as busulfan, melphalan, or thiotepa, offer stronger anti-leukemic effect but at the cost of greater toxicity.

These observations underscore the central question: can a conditioning regimen combine strong anti-leukemic potency with the low toxicity required for older patients undergoing Haplo-SCT? The main objective is to evaluate the efficacy of FT-RIC regimen before Haplo-SCT for older and/or frail patients diagnosed with AML, who are not eligible for a myeloablative conditioning (MAC) regimen.

To achieve this objective, the investigators will assess Progression Free Survival (PFS) defined as the time from allo-HSCT to AML relapse or death.

This is a Multicenter trial, single arm prospective of phase II. Once the conditioning has been administered and the transplant performed, the patient will receive standard routine follow-up care, with the addition of questionnaires, and for patients followed at the Institut Paoli Calmettes only, blood samples will be collected.

研究概览

地位

尚未招聘

研究类型

介入性

注册 (估计的)

77

阶段

  • 阶段2

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。

学习联系方式

研究联系人备份

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Patient with age between 60 and 75 years old ; or aged 18-59 years if considered by the investigator for any reason as ineligible for MAC regimen (as defined by the EBMT criteria17), notably in case of HCT-CI ≥ 3 (patients planned by the investigators to receive a RIC regimen in clinical routine practice);
  • Patients with AML according to the ELN2022 classification criteria requiring allo-HSCT including the MDS/AML sub category);
  • Less than 5% bone marrow blast at the time of inclusion (i.e. CR, CRi, CRh, or MLFS after prior treatment, according to ELN 2022);
  • Allo-HSCT planed with a haploidentical donor;
  • Covered by a Healthcare System;
  • Signed informed consent obtained prior to initiation of any study-specific procedures and treatment as confirmation of the patient's awareness and willingness to comply with the study requirements.

Exclusion Criteria:

  • Left ventricular function < 40% ;
  • Renal clearance < 50 mL/min ;
  • Any severe uncontrolled medical condition considered by the investigator as a contraindication for using treosulfan;
  • Pregnant women or those who may become pregnant (without effective contraception) or breastfeeding;
  • Adults under legal protection (guardianship, curatorship, or judicial protection);
  • Inability to comply with the medical follow-up of the trial for geographical, social, or psychological reasons.

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:fludarabine and treosulfan

After screening and inclusion, patients will be given a RIC regimen based on the market-approved association of fludarabine and treosulfan (FT-RIC):

  • Fludarabine (concentrate for solution for injection/infusion) is a marketed purine analogue and antineoplastic agent.
  • Treosulfan (powder for solution for infusion) is a marketed alkylating medication
As per standard practices, patients will be hospitalized during the treatment period. The treatment is administered by the nurses of the department under the responsibility of the investigator.Fludarabine (30 mg/m²/day from day-6 to day-2), iv andTreosulfan (10 g/m²/day from day-4 to day-2), iv

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
The main objective is to evaluate the efficacy of FT-RIC regimen before Haplo-SCT for older and/or frail patients diagnosed with AML, who are not eligible for a MAC regimen.
大体时间:through study completion an average of 4 years
Progression Free Survival (PFS) defined as the time from allo-HSCT to AML relapse or death
through study completion an average of 4 years

次要结果测量

结果测量
措施说明
大体时间
To evaluate adverse events related to the FT combination according to CTCAE V6.0
大体时间:through study completion an average of 4 years
Conditioning related toxicity according to CTCAE V.6.0
through study completion an average of 4 years
To evaluate engraftment after FT-RIC
大体时间:through study completion an average of 4 years
rate of graft failure
through study completion an average of 4 years
To evaluated hematological recovery after FT-RIC
大体时间:after hematological recovery
Cumulative incidence of neutrophil and platelet recovery
after hematological recovery
to evaluate incidence of both acute and chronic GVHD after FT-RIC
大体时间:through study completion an average of 4 years
Cumulative incidence of acute GVHD and Cumulative incidence of chronic GVHD
through study completion an average of 4 years
To evaluate survival, non-relapse mortality and cause of death after FT-RIC
大体时间:through study completion an average of 4 years
Probability of Overall Survival and Probability of GVHD
through study completion an average of 4 years
To evaluate the immunosuppressive therapy duration after FT-RIC
大体时间:through study completion an average of 4 years
Prevalence of immunosuppressive therapy (IST) and GVHD at 3, 6, 9, 12 months
through study completion an average of 4 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。

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 (估计的)

2026年10月10日

初级完成 (估计的)

2030年10月10日

研究完成 (估计的)

2031年2月10日

研究注册日期

首次提交

2026年2月27日

首先提交符合 QC 标准的

2026年5月19日

首次发布 (实际的)

2026年5月20日

研究记录更新

最后更新发布 (实际的)

2026年5月20日

上次提交的符合 QC 标准的更新

2026年5月19日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • FT-RIC-HAPLO-IPC 2025-016
  • 2025-523632-39-00 (克蒂斯)

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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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