Status:

COMPLETED

Interplay Between Immune and Metabolic Programs in Myelodysplastic Syndromes

Lead Sponsor:

University Hospital, Toulouse

Conditions:

Myelodysplastic Syndromes

Eligibility:

All Genders

18-99 years

Brief Summary

Myelodysplastic syndromes (MDS) are a pre-leukemic condition with an extremely poor prognosis despite current treatments that justify new therapeutic approaches. Various studies have described the pot...

Detailed Description

Myelodysplastic syndromes (MDS) are a pre-leukemic condition with an extremely poor prognosis despite current treatments. It is the most frequent haematological disorder after the age of 65. Different...

Eligibility Criteria

Inclusion

  • Patients:
  • Patient over 18 years of age with a myelodysplastic syndrome (WHO 2016 classification) of low risk (LR=IPSS-R\<4.5) or high risk (HR=IPSS-R\>4.5);
  • Patient naïve to specific treatment of MDS;
  • Patient who expressed no opposition to participating in the study. ;
  • Patient affiliated with the social security system.
  • Control:
  • over 18 years of age,
  • Sample from blood donation (regardless of age) Or Patient \>60 years old, see at the geriatrics platform of the hospital la Grave (CHU of Toulouse),
  • having expressed his non opposition to participate in the study

Exclusion

  • Patients:
  • Myeloid disease other than MDS (including chronic myelomonocytic leukemia and MDS/SMP) ;
  • Ongoing treatments for MDS (excluding erythropoietin, granulocyte colony-stimulating factor and transfusions) ;
  • Medical conditions that may interfere with immune system testing: active cancer, active autoimmune disease, inflammatory conditions, immunosuppressive therapy. ; \* Pregnant or breastfeeding women ; Patient's refusal ;
  • Person benefiting from a system of protection for adults (including guardianship, curators and safeguarding of justice)
  • Control:
  • Medical conditions that may interfere with immune system testing: active cancer, active autoimmune disease, inflammatory conditions, immunosuppressive therapy. ; \* Pregnant or breastfeeding women ;
  • Patient's refusal ;
  • Person benefiting from a system of protection for adults (including guardianship, curators and safeguarding of justice)

Key Trial Info

Start Date :

February 23 2021

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

January 1 2024

Estimated Enrollment :

137 Patients enrolled

Trial Details

Trial ID

NCT04803721

Start Date

February 23 2021

End Date

January 1 2024

Last Update

February 4 2025

Active Locations (1)

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1

IUCT-Oncopole University Hospital

Toulouse, France, 31500