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临床试验/NCT02047578
NCT02047578招募中2 期

Targeted Busulfan, Fludarabine, Etoposide Conditioning Regimen for Hematopoietic Stem Cell Transplantation in Childhood and Adolescent Acute Lymphoblastic Leukemia

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2014年2月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
38
试验地点
1
主要终点
1-year event free survival after hematopoietic stem cell transplantation.

研究概览

简要总结

To evaluate the outcome of hematopoietic stem cell transplantation using targeted busulfan, fludarabine, etoposide conditioning regimen in childhood and adolescent ALL.

详细描述

Busulfan is a highly toxic drug with narrow therapeutic window used for the conditioning of hematopoietic stem cell transplantation. High exposure is associated with systemic toxicity such as veno-occlusive disease (VOD) and underexposure is associated with graft failure or relapse. In this study the investigators plan to improve the outcome of hematopoietic stem cell transplantation by using optimal busulfan dose through pharmacokinetic study.

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 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are diagnosed as ALL.
  • Patients who need hematopoietic stem cell transplantation
  • Age: up to 21 years
  • Performance status: ECOG 0-
  • Patients must be free of significant functional deficits in major organs, but the following eligibility criteria may be modified in individual cases.
  • Heart: a shortening fraction > 30% and ejection fraction > 45%.
  • Liver: total bilirubin < 2 × upper limit of normal; ALT < 3 × upper limit of normal.
  • Kidney: creatinine <2 × normal or a creatinine clearance (GFR) > 60 ml/min/1.73m
  • Patients must lack any active viral infections or active fungal infection.
  • Appropriate donor is available: Matched in 6/6 of A, B, DR loci.
  • Patients (or one of parents if patients age < 19) should sign informed consent.

排除标准

  • Pregnant or nursing women.
  • Malignant or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complications of study therapy.
  • Psychiatric disorder that would preclude compliance.

研究组 & 干预措施

Busulfan

Experimental

Drug: Busulfan First dose: busulfan (120 mg/m2 ivs once daily) (if age<1 yr: 80 mg/ m2) Second to forth dose: according to the daily pharmacokinetic study

干预措施: Busulfan (Drug)

结局指标

主要结局

1-year event free survival after hematopoietic stem cell transplantation.

时间窗: at 1 year

To evaluate 1-year event free survival after hematopoietic stem cell transplantation.

次要结局

  • Engraftment rate(1, 3, 6 and 12 months after transplantation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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