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临床试验/NCT01919866
NCT01919866Unknown1 期

Haploidentical Stem Cell Transplantation With CD3/CD19 Depleted Stem Cells in Pediatric Patients With Refractory Hematological and Oncological Diseases

University Children's Hospital Tuebingen7 个研究点 分布在 2 个国家目标入组 120 人开始时间: 2004年3月最近更新:
适应症

试验速览

阶段
1 期
入组人数
120
试验地点
7
主要终点
Engraftment rate and transplant related mortality

研究概览

简要总结

Feasibility and toxicity of haploidentical transplantation of CD3/CD19 depleted stem cells in combination with a toxicity reduced conditioning regimen or with standard conditioning regimens according to underlying disease.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Year 至 25 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • patients with primary refractory or relapsed disease (including relapse after previous SCT and active disease)
  • AML in complete remission of refractory
  • MDS RAEB-t/secondary AML
  • Non-Hodgkin Lymphoma / Hodgkin Lymphoma
  • non malignant diseases (aplastic anemia, thalassemia, SCID)
  • relapsed Neuroblastoma
  • relapsed soft tissue sarcoma (Rhabdomyosarcoma, Ewing sarcoma, PNET
  • soft tissue sarcoma with primary bone metastases or bone marrow
  • in whom no matched donor was available,

排除标准

  • < 6 months after previous HSCT
  • active cerebral seizure conditions
  • massive progression of leukemias or solid tumours before planned trp.
  • left ventricular ejection fraction <25%
  • creatinine clearance <40ml/min before conditioning
  • respiratory insufficiency with oxygen demand or DLCO <30%
  • Bilirubin >4mg/dl, GOT/GPT >400
  • severe infection (HIV, Aspergillosis)
  • pregnancy

结局指标

主要结局

Engraftment rate and transplant related mortality

时间窗: 365 days

engraftment rate will be evaluated by leukocyte counts in peripheral blood . Definition of engraftment: \>500 neutrophiles/µl blood. Transplant related mortality will be evaluated at day 100 and day 365 post transplant

次要结局

  • Graft versus Host disease and speed of immune reconstitution(365 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Lang

Prof. Dr. med.

University Children's Hospital Tuebingen

研究点 (7)

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