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临床试验/NCT01751997
NCT01751997已完成2 期

The Comparison of Transplantation From Family-mismatched/Haploidentical Donors With Matched Unrelated Donors in Adult Patients With Acute Myeloid Leukemia

Byung-Sik Cho1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2013年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
116
试验地点
1
主要终点
Overall survival

研究概览

简要总结

This study will compare the clinical outcomes of transplants from family-mismatched/haploidentical donors (FMT) with transplants from 8/8-matched unrelated donor (MUT), which is a current gold standard donors when lacking of HLA-matched-siblings

  1. Primary objectives: Overall survival of FMT may be similar to that of MUT
  2. Secondary objectives:

i. Comparison of disease-free survival, relapse, non-relapse mortality, immune reconstitution cytomegalovirus infection, and acute or chronic graft-versus-host disease between FMT and MUT.

ii. Investigation of possible biomarkers related with above events after transplantation

详细描述

For patients lacking an HLA-identical sibling, 8/8-matched unrelated donors are currently the "gold standard" for a donor, since outcomes after HLA-identical sibling have been compared to 8/8-matched unrelated donors. Currently, there are three alternative graft sources, including mismatched unrelated donors, familial mismatch/haploidentical donors, and umbilical cord bloods. Compared with other sources, transplants from familial mismatch/haploidentical donors (FMT) have the benefit of an immediate availability of a donor, particularly for those patients who urgently need transplantation. Initial reports had characterized FMT to a poor engraftment and a high incidence of graft-versus-host disease. However, outcomes of FMT have significantly improved over the past decade in the optimization of conditioning regimen and graft selection to allow a stable engraftment across major HLA barriers, with promising leukemia-free survival in adults with acute leukemia. Despite the encouraging results and potential benefit of FMT, there have been few studies comparing clinical outcomes of FMT with other donor types, particularly in acute myeloid leukemia (AML) as a single disease. Since August 2008, we have been continuously performing FMT using unmanipulated donor cells and a less aggressive conditioning regimen in high-risk AML lacking an HLA-identical sibling, 8/8 or 7/8-matched unrelated donors. We reported the feasibility of FMT using our novel reduced-intensity regimen without ex vivo T-cell depletion, showing early results similar to outcomes of transplant from 8/8-matched unrelated donors (MUT). This study will test the hypothesis that overall survival at 3 years after FMT is similar to overall survival after MUT.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
17 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Transplants from 8/8-matched unrelated

Active Comparator

Participants will receive transplants from 8/8-matched unrelated donors using myeloablative or reduced-intensity conditioning according to age or comorbidity.

干预措施: Transplants from 8/8-matched Unrelated donors (Drug)

Transplants from family-mismatched/haploidentical donors

Experimental

Participants will receive FMT using a reduced intensity conditioning regimens.

干预措施: Transplants from family-mismatched/haploidentical donors (Drug)

结局指标

主要结局

Overall survival

时间窗: annually through 3 years

Overall survival is defined as the time interval between date of enrollment and death from any cause or for surviving patients, to last follow-up

次要结局

  • Neutrophil recovery(56 days)
  • Donor cell engraftment(56 days)
  • Acute graft-versus-host disease (aGVHD)(every 3 months through 3 years)
  • Chronic graft-versus-host disease (cGVHD)(every 3 months through 3 years)
  • T cells reconstitution(before and 2 weeks and 1 month after transplantation, then every 3 months through 1 year)
  • Secondary Graft failure(100 days)
  • NK cells reconstitution(before and 2 weeks and 1 month after transplantation, then every 3 months through 1 year)
  • B cells reconstitution(before and 2 weeks and 1 month after transplantation, then every 3 months through 1 year)
  • Primary Graft failure(56 days)
  • Platelet recovery(100 days and 180 days)
  • Non-relapse mortality(annually through year 3)
  • WT1 MRD assessment(before and 1 month after transplantation, then every 3 months through 3 years)
  • BAALC MRD assessment(before and 1 month after transplantation, then every 3 months through 3 years)
  • Disease free survival(annually through year 3)
  • Infection(annually through year 3)
  • NGS-based MRD assessment(before and 1 month after transplantation, then every 3 months through 3 year)

研究者

发起方
Byung-Sik Cho
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Byung-Sik Cho

Assistant Professor

Seoul St. Mary's Hospital

研究点 (1)

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