Actively Recruiting

Age: 18Years +
All Genders
NCT06022328

Impact of Epigenetic Age on Clinic-biological Presentation and Prognosis in Myeloproliferative Neoplasms Epigenetic Age in Myeloproliferative Neoplasms (EpiC)

Led by University Hospital, Bordeaux · Updated on 2025-07-30

120

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Myeloproliferative Neoplasms (MPN) are hematological malignancies characterized by the excessive production of myeloid cells. MPN can be complicated by thrombosis and evolution into more aggressive diseases (myelofibrosis and acute leukemia). Aging remains the principal factor determining patients' survival in MPN. In recent years, DNA methylation has appeared as a mean to measure aging via the development of epigenetic clocks that have also been associated with the occurrence of thrombosis and cancer. The epiC project aims at determining epigenetic age of MPN patients and search for an association between this parameter and thrombotic/hematological complications.

CONDITIONS

Official Title

Impact of Epigenetic Age on Clinic-biological Presentation and Prognosis in Myeloproliferative Neoplasms Epigenetic Age in Myeloproliferative Neoplasms (EpiC)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Polycythemia Vera, Essential Thrombocythemia, or Primary Myelofibrosis
  • Have DNA extracted from purified granulocytes collected at diagnosis
  • Not currently receiving treatment that impacts DNA methylation such as chemotherapy or immunosuppressants
  • For control subjects without MPN: no hematological malignancy and tested for JAK2V617F mutation due to reactive thrombocytosis or secondary polycythemia
  • Control subjects also must not be receiving treatments affecting DNA methylation
Not Eligible

You will not qualify if you...

  • Diagnosed with conditions other than Polycythemia Vera, Essential Thrombocythemia, or Primary Myelofibrosis
  • No purified granulocyte DNA available from time of diagnosis
  • Receiving cytoreductive drugs, demethylating agents, chemotherapy, or immunosuppressive therapy at DNA sampling
  • Less than 2 years of follow-up after diagnosis
  • For control subjects: presence of hematological malignancy or solid cancer
  • Control subjects receiving treatments affecting DNA methylation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de Bordeaux, service Hématologie Biologique

Bordeaux, France

Actively Recruiting

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Research Team

O

Olivier MANSIER

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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