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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
France
CHU de Nice
RECRUITING
Nice
Contact Information
Primary
Thomas Cluzeau, Professor
cluzeau.t@chu-nice.fr
0492039025
Backup
Lydia Cherfaoui
cherfaoui.l@chu-nice.fr
0492039025
Time Frame
Start Date: 2026-02-09
Estimated Completion Date: 2028-02-09
Participants
Target number of participants: 52
Treatments
No_intervention: Hemoglobin-Based Transfusion Strategy
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
Experimental: Quality of Life-Guided Transfusion Strategy
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
Sponsors
Leads: Centre Hospitalier Universitaire de Nice

This content was sourced from clinicaltrials.gov