Ferroptosis Study in SF3B1-mutant Myelodysplastic Syndromes (FerMDS)
Condition(s) studied
Investigational drug(s) / intervention(s)
Biological sampling: The procedure will consist of an additional bone marrow sample and blood sample
Study summary
Myelodysplastic syndromes (MDS) are clonal diseases of hematopoietic stem cells (HSC) characterized by dysplastic and inefficient hematopoiesis related to excessive progenitor cell death. Ferroptosis is a recently described cell death mechanism and we think that it could be a major player in the pathophysiology of MDS, involved in the cell death that characterizes these diseases and contributing to cytopenias. The study aims to demonstrate that there is a significant activation of this phenomenon in MDS patients compared to a population of subjects without MDS.
Eligibility
Primary outcome measure(s)
- Percentage of cells undergoing ferroptosis in SF3B1-mutant MDS patients compared to MGUS patients — At Baseline
Mean values for the proportion of ferroptose cells will be compared between arms, using comparative statistical methods (Student's t test, Student's test for unequal variances or Wilcoxon test)
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Bordeaux, Laboratoire d'Hématologie | Pessac | France | Not Yet Recruiting |
| CHU de Bordeaux, Service de Médecine Interne | Pessac | France | Not Yet Recruiting |
| CHU de Bordeaux, Service Hématologie Clinique et Thérapie Cellulaire | Pessac | France | Recruiting |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05924074 on ClinicalTrials.gov ↗ ← All trials in France