Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT04869683

Biocollection in MyeloDysplastic Syndrome (P-MDS)

Led by University Hospital, Brest · Updated on 2025-02-05

150

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Myelodysplastic syndromes (MDS) are chronic myeloid hemopathies characterized by ineffective hematopoiesis (with peripheral cytopenias) and which contrast with a marrow of normal richness. MDS is considered one of the four most common blood diseases. The incidence is estimated at 4,059 cases / year in 2012 with an average age of 78 years in men and 81 years in women (INCA report, Cancers in France in 2015). The incidence increases with lengthening of the lifespan. The main risk of MDS is transformation to acute leukemia in 30 to 40% of cases. Treatment options depend on clinical, hematologic and chromosomal abnormalities. The prognosis is considered to be at low or high risk of developing acute leukemia. This distinction will therefore have an impact on the therapeutic solution (s). MDS exhibit clinical, morphological and genetic heterogeneity. It is therefore necessary to form subgroups of patients to better understand the physiopathogenesis of this pathology. The constitution of a biocollection will make it possible to search for clinical and biological prognostic markers in order to identify patients progressing to acute myeloid leukemia.

CONDITIONS

Official Title

Biocollection in MyeloDysplastic Syndrome (P-MDS)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient diagnosed with or suspected of having myelodysplastic syndrome (WHO definition) at diagnosis or during follow-up
  • Managed at the Cancer-Hematology Institute of the Brest CHRU
  • Presence of biological material collected within the CRB
  • Patient's consent obtained
Not Eligible

You will not qualify if you...

  • Minor or pregnant woman
  • No biological material collected within the CRB
  • Refusal to participate or unable to consent
  • Patient under judicial protection such as guardianship or curatorship

AI-Screening

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Trial Site Locations

Total: 1 location

1

Chu Brest

Brest, France, 29609

Actively Recruiting

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Research Team

N

Nathalie Douet-Guilbert, MD, PhD

CONTACT

M

Marie-Bérengère Troadec, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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