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临床试验/NL-OMON38951
NL-OMON38951已完成不适用

Treatment guided by detection of Minimal Residual Disease after allogeneic stem cell transplantation in Acute Myeloid Leukaemia - VUHEM-MRD-2013

Vrije Universiteit Medisch Centrum0 个研究点目标入组 31 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
31

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • *Patients with Acute Myeloid Leukemia according to WHO classification 2008
  • *Age 18-75
  • *Indication for allogeneic stem cell transplantation based on risk group profile
  • *Related or unrelated 8/8 HLA matched donor available
  • *Presence of Leukemia Associated Phenotype(s) (LAPs)
  • *Written informed consent

排除标准

  • -Myelodysplastic syndrome with refractory anaemia with excess blasts (RAEB)
  • Acute Promyelocytic Leukemia (AML M3)
  • -Absence of LAP(s)
  • -Previous allogeneic stem cell transplantation
  • -Severe cardiovascular disease (arrhythmias requiring chronic treatment, congestive heart failure or symptomatic ischemic heart disease)
  • *Severe pulmonary dysfunction (CTCAE grade III-IV, see appendix D)
  • *Severe neurological or psychiatric disease
  • *Significant hepatic dysfunction (serum bilirubin or transaminases * 3 times upper limit of normal) unless related to treatment
  • *Significant renal dysfunction (creatinine clearance < 30 ml/min after rehydration)
  • *Concurrent severe and/or uncontrolled medical condition (e.g. uncontrolled diabetes, infection, hypertension, cancer, etc.)
  • *Patient known to be HIV-positive
  • *Pregnant or breast-feeding female patients
  • *Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol and follow-up schedule

研究者

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