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临床试验/NCT05558943
NCT05558943尚未招募不适用

Study of Management and Prognosis of Patients With Acute Myeloblastic Leukemia in Saint-Antoine Hospital

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2025年10月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
750
试验地点
1
主要终点
Overall survival

研究概览

简要总结

AML in adults represents a group of heterogeneous diseases; the prognosis remains poor despite significant therapeutic advances in recent years. In order to optimize patient care, it is necessary to have "real life" data that exhaustively reports on the patients treated in our department. The objective of this study is:

  • To describe the AML treated within the hematology department
  • To optimize the management of patients with AML.

详细描述

Current state of knowledge:

Acute myeloblastic leukemia are the most common leukemias in adults. This pathology is very heterogeneous. It has a poor prognosis despite numerous therapeutic advances. The lack of randomized clinical trials can make certain treatment decisions difficult. In addition, patients with comorbidities or the elderly are most often excluded from these trials even though they represent a significant proportion of new diagnoses.

Objectives:

Primary objective Evaluate the overall survival of adult patients treated for AML in our hematology department at Saint-Antoine Hospital.

Secondary objectives

研究设计

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

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

  • Age :18 years and older
  • Patients with AML
  • Non objection to research

排除标准

  • Minor patients
  • Acute promyelocytic leukemia (AML3)

结局指标

主要结局

Overall survival

时间窗: 2 years after diagnosis

次要结局

  • Incomplete cytological remission rate(after the phase of induction up to 24 months)
  • Side effects(24 months)
  • Cytological remission rate(after the phase of induction up to 24 months)
  • Leukemia free survival rate(24 months)
  • the rate of patients receiving intensive treatment(24 months)
  • Overall survival(1 year after diagnosis)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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