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临床试验/NCT00716690
NCT00716690Unknown1 期

Enhancement of Hematopoietic Stem Cell Engraftment by Multi Donor Stem Cell Transplantation (MDT) From 2 Mismatched Donors, a Phase I-II Open Study

Hadassah Medical Organization1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2008年7月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
入组人数
10
试验地点
1
主要终点
Day of neutrophil engraftment

研究概览

简要总结

The proposed research focuses on the development of innovative protocol of mismatched stem cell transplantation with combined 2 different haplo stem cell transplantation (SCT) donors which are mismatched to the recipient (and preferably to each other), in a patient in need for SCT, lacking an HLA match related or an unrelated donor. This innovative protocol named multi donor stem cell transplantation (MDT) is designed to facilitate engraftment even when reduced intensity conditioning or a low cell dose are used, improve the graft vs. leukemia (GVL) effect and enhance immune reconstitution (using quantitative and qualitative parameters).

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
— 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patient age 0-70 years old with leukemia in 1st remission at high risk of relapse because of unfavorable prognostic features, at 2nd CR or MDS without an readily available matched donor (related or unrelated).
  • •Patients must have a mismatched donor willing and capable of donating peripheral blood stem cells and/or bone marrow progenitor cells using conventional techniques, and lymphocytes if indicated (mismatched defined as 3/6-4/6 HLA matching).
  • •Each patient / patient's guardian must sign written informed consent.
  • •Patients must have an ECOG PS ≤ 2; Creatinine <2.0 mg/dl; Ejection fraction >40%; DLCO >50% of predicted; Serum bilirubin <3 gm/dl; elevated GPT or GOT <3 x normal values.

排除标准

  • •Not fulfilling any of the inclusion criteria.
  • •Not in CR (if the indication for transplant is leukemia).
  • •Active life-threatening infection.
  • •Overt untreated infection.
  • •HIV seropositivity, Hepatitis B or C antigen positivity with evidence of active hepatitis.
  • •Pregnant or lactating women.
  • •Donor contraindication (HIV seropositive confirmed by Western Blot, Hepatitis B antigenemia, HCV, evidence of bone marrow disease, unable to donate bone marrow or peripheral blood due to concurrent medical condition).
  • •Previous autologous or allogeneic stem cell transplantation.
  • •Inability to comply with study requirements.

研究组 & 干预措施

treatment

Experimental

干预措施: Multi donor stem cell transplantation (Procedure)

结局指标

主要结局

Day of neutrophil engraftment

时间窗: 30d

Day of platelet engraftment>20x10(9)L

时间窗: 30

Acute GVHD occurrence>2

时间窗: 100d

Disease free survival

时间窗: 100d

次要结局

  • Immune reconstitution(100d)
  • Transplant related toxicity(100d)
  • Day of platelet engraftment>50x10(9)/L(30d)
  • Time of acute GVHD(100d)
  • GVHD grade(100d)
  • Overall survival(100 days)
  • Infections incidence(100d)
  • transplant-related mortality(100d)

研究者

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

SHAPIRA MICHAEL

Prof Shapira

Hadassah Medical Organization

研究点 (1)

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