Essential Thrombocythemia, Polycythemia Vera, Primary Myelofibrosis
Conditions
Brief summary
All patients diagnosed or followed in Brest University Hospital for Philadelphia negative myeloproliferative neoplasms will be included in this observational study. Myeloproliferative neoplasms recorded included: polycythemia vera, essential Thrombocythemia and Primary Myelofibrosis. This is a not interventional study. Alive patients need to sign a non-opposition consent form. Patients will be followed until last news (death, change of reference centre...).
Detailed description
In this retrospective and prospective study, clinical and biological data from diagnosis until last news will be recorded. Clinical data collected: patients and disease characteristics at the time of the diagnosis, disease and mutational status, cardio-vascular risk factors, history of thrombosis and cancer. Biological data collected: hemogram and bone marrow results if available. During the follow-up new data will be noted: treatment changes (reasons of change and type of drug), thrombotic events (localization, date and hemogram), phenotypic evolutions (type and date), death (date and etiology).
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with essentiel thrombocythemia, polycythemia vera or primary myelofibrosis * Signature of the non-opposition consent form
Exclusion criteria
* None
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival | 10 years | occurrence of death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of evolutions | 10 years | occurrence of transformation into polycythemia vera, secondary myelofibrosis, myelodysplastic syndrome or acute leukemia |
| Incidence of thromboses | 10 years | occurrence of arterial or venous thrombotic events |
Countries
France