跳至主要内容
临床试验/NCT02693899
NCT02693899已完成不适用

Monocentric, Biological, Uncontrolled, Prospective Study on the Feasibility of Plasma FLT3 Ligand Assay to Achieve a First Estimate of Its Prognostic Value on the Outcome of Patients Treated With Intensively for Acute Leukemia

Nantes University Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2016年5月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
1
主要终点
Dosage of plasma FLT3-L in adult patients with acute leukemia

研究概览

简要总结

Despite advances in their classification and treatment, acute leukemia remain incurable disease for the majority of patients. It is necessary to identify new prognostic markers of survival and new therapeutic targets to improve prognosis. Some studies have shown that Fms-like tyrosine kinase 3-ligand (FLT3-L) could be interesting from this. A more recent study from our group testing a novel therapy in acute lymphoblastic leukemia, showed an increase of this marker in the blood of patients responding to treatment. The aim of our prospective, non-interventional study is to measure the plasma levels of FLT3-L at different times of the management of patients with acute lymphoblastic leukemia but also myeloid. For this, analyzes of the samples collected in the usual care will be conducted to study the relationship between the plasma concentration of FLT3-L and outcomes. If there is any link, the FLT3-L could serve as a predictor of treatment response.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Acute myelogenous leukemia diagnosis or lymphoblastic
  • Patient intensively treated
  • Patients who agreed to participate in the study and having signed the consent biocollection
  • Non-Inclusion Criteria:
  • Patient aged under 18

排除标准

  • 未提供

结局指标

主要结局

Dosage of plasma FLT3-L in adult patients with acute leukemia

时间窗: up to three months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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