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Clinical Trial Summary

Prospective study to decipher the clonal architecture of ASXL1-mutated primary and secondary myelofibrosis and its impact on prognosis


Clinical Trial Description

The clonal architecture of myelofibrosis patients is still little described. Inconsistent results in terms of the prognostic value of some mutations are observed in the literature, in particular concerning ASXL1 mutations. We assume that a better understanding of the clonal architecture of ASXL1-mutated myelofibrosis could help refining the prognostic impact of ASXL1 mutations. This study aims to evaluate a multicenter cohort of 50 patients. Blood of patients will be collected within 18 months of diagnosis. After 4 years of follow-up of the patient as part of his usual care, data on survival and leukemic transformation will be collected. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05710211
Study type Interventional
Source University Hospital, Angers
Contact Margaux Wiber, PharmD.
Phone 0033241355553
Email margaux.wiber@chu-angers.fr
Status Not yet recruiting
Phase N/A
Start date March 2023
Completion date March 2029

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