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临床试验/NCT07328191
NCT07328191招募中不适用

Quality of Life-based Transfusion in Refractory MDS or AML Under Advanced Palliative Care and Supportive Treatment.

Centre Hospitalier Universitaire de Nice1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2026年2月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
52
试验地点
1
主要终点
Number of Red Blood Cell Transfusions

研究概览

简要总结

Patients with refractory myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML) in exclusive palliative care frequently receive red blood cell transfusions based on hemoglobin thresholds, despite limited evidence of clinical benefit in this setting.

This prospective randomized study compares a standard hemoglobin-based transfusion strategy to a quality-of-life-guided strategy using the EQ-5D-5L questionnaire, with the aim of reducing transfusion burden while maintaining patient safety and quality of life.

详细描述

This is a prospective, single-center, randomized interventional study conducted in patients with transfusion-dependent refractory MDS or AML receiving exclusive palliative care. Palliative Care

Patients are randomized to either a standard transfusion strategy based on hemoglobin thresholds or a quality-of-life-guided strategy in which red blood cell transfusions are triggered by a clinically significant deterioration in EQ-5D-5L score.

The study aims to evaluate whether a quality-of-life-guided transfusion strategy can safely reduce the number of red blood cell transfusions without negatively impacting patient-reported outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged 18 years and older.
  • Diagnosis of refractory MDS or AML, receiving palliative care only.
  • Anaemia with haemoglobin ≤ 8 g/dl at inclusion (or ≤ 9 g/dl if associated with cardiovascular disease).
  • Transfusion dependency, defined as requiring more than 2 GR transfusions every 8 weeks.
  • No vitamin B9, vitamin B12 or iron deficiency.
  • Ability to understand and sign the informed consent form.
  • Ability to comply with the schedule of visits and other protocol requirements.
  • Non inclusion Criteria:
  • Previous malignant disease other than MDS or AML (except basal cell or squamous cell carcinoma or carcinoma in situ of the cervix or breast).
  • Active uncontrolled infection (hepatitis B or C, HIV).
  • Use of G-CSF.
  • Confirmed neurocognitive disorders (based on prior diagnosis or clinical assessment by the investigator) impairing comprehension, consent or the ability to reliably complete the EQ-5D-5L questionnaire.
  • Active uncontrolled heart disease.
  • Active haemolytic anaemia.
  • Recent major surgery.
  • Life-threatening complications of MDS/AML.
  • Presence of another serious or unstable disease which, in the investigators' opinion, would make participation in the study inappropriate or risky for the patient's safety.
  • Vulnerable individuals.

排除标准

  • Immediate severe complications related to MDS/AML, such as uncontrolled bleeding, pneumonia with hypoxia or shock, or severe disseminated intravascular coagulopathy.
  • Withdrawal of the patient's voluntary informed consent.

研究组 & 干预措施

Hemoglobin-Based Transfusion Strategy

No Intervention

Red blood cell transfusions are performed according to standard hemoglobin thresholds (Hb <7 g/dL, or <8 g/dL in patients with cardiovascular comorbidities). Standard of care arm

Quality of Life-Guided Transfusion Strategy

Experimental

Red blood cell transfusions are performed when a clinically significant deterioration (≥1 level decrease in at least one EQ-5D-5L domain compared to baseline) is observed

干预措施: Red blood cell transfusions based on EQ-5D-5L questionnaire (Other)

结局指标

主要结局

Number of Red Blood Cell Transfusions

时间窗: 2 months

Total number of red blood cell units transfused during the 2-month follow-up period.

次要结局

  • Quality of Life (EQ-5D-5L)(from baseline to 1 month and 2 months.)
  • Overall Survival(from inclusion to 2 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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