Clinical trial · Observational
Clinical and Therapeutic Impact of Molecular Markers in Myeloproliferative Disorders
Clinical and Therapeutic Impact of Molecular Markers in Myeloproliferative Neoplasms (CTIM3)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Myeloproliferative neoplasms (MPN) are clonal hematopoietic disorders sharing a common natural evolution: a chronic phase, characterized by a major risk of vascular events, followed by an accelerated phase eventually leading to transformation to acute leukemia. MPN include polycythemia vera, essential thrombocythemia, primary myelofibrosis, and rarer entities. During the past years, CML became a paradigm for targeted therapy and personalized cancer medicine. For other MPNs, the discovery of the JAK2V617F mutation followed by many other mutations, opened similar perspectives. However, several questions remain to be answered in MPNs regarding the clinical implication of these major scientific discoveries: what is the clinical impact of JAK2V617F and other molecular biomarkers on the risks of complications and progression? Can these new biomarkers be used in the perspective of a personalized therapy of MPNs? his project will focus on the qualification of a series of known mutations as biomarkers in MPNs based on large multicenter cohorts of patients with well-annotated samples
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myeloproliferative Neoplasms | Myeloproliferative Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- cumulative incidence or progression
- timeFrame
- inclusion
Secondary outcomes (4)
- measure
- Disease phenotype according to WHO classification
- timeFrame
- 3 years
- description
- polycythemia vera, essential thrombocythemia, primary myelofibrosis, and others
- measure
- Treatment response/resistance
- timeFrame
- 3 years
- measure
- Mean life-years gained
- timeFrame
- 3 years
- description
- The analysis will take into consideration the cost of testing, but also the costs of different treatment options with or without testing, and other disease-related costs dependent on treatment
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * Patients suffering from Myeloproliferative neoplasms (MPN) diagnosed between 2005 and 2013 * Sample DNA diagnostics available: 500 mcg * Untreated or treated with hydroxyurea, ruxolitinib, alpha interferon, * Patient has given his(her) own consent for the use of the sample for research on the pathology and genetic analyzes Exclusion Criteria: * Refused to participate * Patient treated with another molecule that hydroxyurea, ruxolitinib, or alpha interferon
References
Publications (0)
Data not yet available