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临床试验/NCT07052422
NCT07052422尚未招募2 期

Venetoclax+Decitabine+Busulfan+Fludarabine (VEN+DAC+Bu2Flu4) vs Busulfan+Fludarabine Conditioning Regimen (Bu2Flu5 ) for Older Patients With Myeloid Malignancies Undergoing Allogeneic Hematopoietic Stem Cell Transplantation (Allo-HSCT)

Nanfang Hospital, Southern Medical University0 个研究点目标入组 160 人开始时间: 2025年7月15日最近更新:
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
160
主要终点
Disease-free survival (DFS) rate

研究概览

简要总结

The purpose of this study is to compare the efficacy and safety of venetoclax+decitabine+busulfan+fludarabine (VEN+DAC+Bu2Flu4) regimen with busulfan+fludarabine (Bu2Flu5) regimen in older patients with myeloid malignancies undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).

详细描述

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potent curative approach for myeloid malignancies, but outcomes post-transplantation of older population were unsatisfactory. The conditioning regimen is an essential factor affecting outcomes post-transplantation. Currently, the optimal conditioning for older patients with myeloid malignancies remains unclear. Myeloablative conditioning (MAC) regimens like busulfan plus cyclophosphamide, and busulfan plus fludarabine (Bu4Flu4-5) have low relapse rates, but high non-relapse mortality (NRM) is observed in older patients with myeloid malignancies. The development of reduced-intensity conditioning (RIC) regimens such as Bu2Flu5 has decreased NRM and enhanced the feasibility of allo-HSCT in older patients with myeloid malignancies, but it appears to have higher relapse rate. Neither conventional MAC nor RIC regimens benefit older patients with myeloid malignancies. In recent years, some studies reported that the introduction of venetoclax (VEN) or decitabine (DAC) to MAC reduced relapse without increasing NRM in younger patients with high-risk myeloid malignancies. However, whether VEN and DAC combined with RIC regimen reduce relapse without increasing NRM, then improve survival in older patients with myeloid malignancies is unclear. Therefore, we conducted a randomized controlled study to compare the efficacy and safety of VEN+DAC+Bu2Flu4 with Bu2Flu5 in older patients with myeloid malignancies undergoing allo-HSCT.

研究设计

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

入排标准

年龄范围
60 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 60-75 years
  • Acute myeloid leukaemia in first complete remission or myelodysplastic syndrome
  • Willing to undergo the first allo-HSCT
  • Eastern Cooperative Oncology Group performance status of 0-2

排除标准

  • Any abnormality in a vital sign (e.g., heart rate, respiratory rate, or blood pressure)
  • Patients with any conditions not suitable for the trial (investigators' decision)

研究组 & 干预措施

VEN+DAC+Bu2Flu4

Experimental

Venetoclax+Decitabine+Busulfan+Fludarabine

干预措施: Venetoclax (VEN) (Drug)

VEN+DAC+Bu2Flu4

Experimental

Venetoclax+Decitabine+Busulfan+Fludarabine

干预措施: Decitabine (DAC) (Drug)

VEN+DAC+Bu2Flu4

Experimental

Venetoclax+Decitabine+Busulfan+Fludarabine

干预措施: Busulfan (Bu) (Drug)

VEN+DAC+Bu2Flu4

Experimental

Venetoclax+Decitabine+Busulfan+Fludarabine

干预措施: Fludarabine (Flu) (Drug)

Bu2Flu5

Active Comparator

Busulfan+Fludarabine

干预措施: Busulfan (Bu) (Drug)

Bu2Flu5

Active Comparator

Busulfan+Fludarabine

干预措施: Fludarabine (Flu) (Drug)

结局指标

主要结局

Disease-free survival (DFS) rate

时间窗: 2 year

Will calculate time from random assignment until disease progression or relapse or death from any cause

次要结局

  • Overall survival (OS) rate(2 year)
  • Relapse incidence(2 year)
  • Non-relapse mortality (NRM) incidence(2 year)

研究者

申办方类型
Other
责任方
Sponsor

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