跳至主要内容
临床试验/jRCTs031220607
jRCTs031220607招募中不适用

Phase II study of salvage haploidentical allogeneic hematopoietic stem cell transplantation using posttransplant cyclophosphamide for engraftment failure (JSCT Salvage PTCy-Haplo)

未提供0 个研究点目标入组 20 人开始时间: 2023年7月5日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
20
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
No limit 至 70age old under(—)
性别
All

入选标准

  • primary engraftment failure after allogeneic hematopoietic stem cell transplantation for hematological disease, primary immunodeficiency, and congenital metabolic disorder
  • any stage and disease status
  • any history of autologous or allogeneic stem cell transplantation
  • no evidence of severe organ dysfunction (ejection fraction >=50, total bilirubin <=2.0, CCr >=30, SpO2 >=90% (O2 <=4L/min)
  • consent to join this study
  • a HLA haploidentical donor is available

排除标准

  • positive anti-HIV antibody
  • active cancer
  • need for vasopressor
  • allergic to cyclophosphamide, melphalan, fludarabine, tacrolimus, and mycophenolate Mofetil
  • need for chemotherapy before protocol therapy
  • concomitant relapse of primary malignancy
  • recurrent engraftment failure
  • presence of donor-specific anti-HLA antibody
  • judgment by physician

结局指标

主要结局

-

Overall survival at 1 year

次要结局

  • neutrophil and platelet engraftment rate(30 days)
  • incidence and severity of acute and chronic GVHD(180 and 365 days)
  • relapse rate(180 and 365 days)
  • nonrelapse mortality(180 and 365 days)
  • relapse-free survival(180 and 365 days)
  • GVHD-free relapse-free survival(180 and 365 days)
  • incidence of infection(180 days)
  • incidence of non-hematological toxicity graded>=3(100 days)

研究者

发起方
未提供

相似试验