跳至主要内容
临床试验/NCT02823210
NCT02823210Unknown不适用

Clinical and Therapeutic Impact of Molecular Markers in Myeloproliferative Neoplasms (CTIM3)

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2016年6月最近更新:
适应症

试验速览

阶段
不适用
入组人数
300
试验地点
1
主要终点
cumulative incidence or progression

研究概览

简要总结

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

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Refused to participate
  • Patient treated with another molecule that hydroxyurea, ruxolitinib, or alpha interferon

结局指标

主要结局

cumulative incidence or progression

时间窗: inclusion

次要结局

  • Treatment response/resistance(3 years)
  • Disease phenotype according to WHO classification(3 years)
  • Mean life-years gained(3 years)
  • Quality-adjusted life years gained(3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验