Groupe Francophone Des Myelodysplasies

Myelodysplastic Syndromes and Risk-Adapted Care

Research activity centers on myelodysplastic syndromes across low-risk, intermediate-risk, higher-risk, and very high-risk disease, including patients with transfusion-dependent anemia and those who are ineligible for allogeneic transplantation.

  • Lower-risk MDS with anemia
  • Higher-risk MDS and transplant-ineligible disease
  • Myelodysplastic syndromes with transfusion dependence
  • Post-transplant relapse in myeloid disease

Trials also address erythroid failure, hematologic improvement, and disease control in patients who have not responded to standard supportive or disease-directed treatment.

Genetically Defined Myeloid Neoplasms

The sponsor supports studies in IDH1-mutated and IDH2-mutated myelodysplastic syndrome, reflecting interest in molecularly targeted care for clonal myeloid disorders.

  • IDH1-mutated MDS
  • IDH2-mutated MDS
  • Mutationally selected myeloid disease

These studies focus on treatment response and tolerance in molecularly characterized disease subsets.

Chronic Myelomonocytic Leukemia and Overlapping Myeloid Disorders

Clinical research includes higher-risk chronic myelomonocytic leukemia and related myeloid neoplasms, with attention to patients whose disease overlaps with myelodysplastic and acute leukemic features.

  • Higher-risk CMML
  • MDS/AML overlap
  • Relapsed myeloid neoplasms after transplantation

Research in this area addresses disease control in advanced myeloid malignancy and post-transplant recurrence.

VEXAS Syndrome and Autoinflammatory Disease

The sponsor funds research in VEXAS syndrome, a severe autoinflammatory disorder linked to UBA1 mutation and refractory systemic symptoms.

  • VEXAS syndrome
  • UBA1-mutated disease
  • Steroid-refractory inflammatory symptoms

These studies focus on symptom burden and inflammatory control in a rare adult-onset condition with hematologic involvement.

Erythropoiesis and Transfusion Independence

A major theme is treatment of anemia through strategies aimed at improving erythropoiesis and reducing red blood cell transfusion needs in lower-risk MDS.

  • Erythropoiesis-stimulating agent failure
  • Luspatercept-based approaches
  • Transfusion independence
  • Non-transfusion-dependent anemia

Research in this domain also includes optimization of supportive hematologic treatment for patients with persistent symptomatic anemia.

Want to learn more about this study or check if you can participate? Contact us.

Matched clinical trials

  • Study of momelotinib in patients with VEXAS syndrome and myelodysplastic syndrome who are dependent on or do not respond to steroid treatment

    Recruiting

    2 1 1
    Investigated diseases:
    France
  • Study on Oral Arsenic Trioxide for Patients with Low-Risk Myelodysplastic Syndromes Not Responding to Erythropoiesis Stimulating Agents and Luspatercept

    Recruiting

    1 1 1
    Investigated drugs:
    France
  • Study on Luspatercept and Epoetin Alfa for Patients with Low-Risk Myelodysplastic Syndrome Without Ring Sideroblasts Who Did Not Respond to ESA

    Recruiting

    1 1 1 1
    Investigated drugs:
    France Italy
  • Study on the Effectiveness of Enasidenib Mesilate in Patients with Myelodysplastic Syndrome with IDH2 Mutation

    Not recruiting

    2 1 1
    Investigated drugs:
    France Germany
  • Study on the Effectiveness of Ivosidenib in Patients with IDH1 Mutated Myelodysplastic Syndrome

    Not recruiting

    2 1 1 1
    Investigated drugs:
    France
  • Study on Early vs. Late Epoetin Alfa Treatment for Adults with Low-Risk MDS and Anemia Not Requiring Blood Transfusions

    Not recruiting

    3 1 1 1
    Investigated drugs:
    France