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UnknownNCT05453552

G-CSF+DAC+BUCY vs G-CSF+DAC+BF Conditioning Regimen for High-risk MDS Undergoing Allo-HSCT

G-CSF+DAC+BUCY vs. G-CSF+DAC+BF Conditioning Regimen for Patients With High-risk MDS Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
242 (estimated)
Sponsor
Nanfang Hospital, Southern Medical University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Allo-HSCT is the most effective way to cure high-risk MDS patients. At present, the best conditioning regimen for high-risk MDS patients undergoing allo-HSCT remains in discussion. In this prospective study, the safety and efficacy of G-CSF+DAC+BUCY and G-CSF+DAC+BF conditioning regimens in high-risk MDS patients undergoing allo-HSCT are evaluated.

Detailed description

Allo-HSCT is the most effective way to cure high-risk MDS patients. At present, the best conditioning regimen for high-risk MDS patients undergoing allo-HSCT remains in discussion. A previous study by the investigators has showed that G-CSF +DAC+BUCY conditioning regimen could reduce the relapse and improve the survival compared with BUCY conditioning regimen, while the two conditioning regimens both have high non-relapse mortality (NRM). Several retrospective and prospective studies have demonstrated that BF conditioning regimen has a lower NRM compared with BUCY conditioning regimen, while the relapse and survival are similar in patients undergoing BF and BUCY conditioning regimens. Based on the above, the investigators design the prospective randomized controlled study to evaluate the safety and efficacy of G-CSF+DAC+BUCY and G-CSF+DAC+BF conditioning regimens in high-risk MDS patients undergoing allo-HSCT.

Conditions

Interventions

TypeNameDescription
DRUGGranulocyte Colony-Stimulating Factor(G-CSF)G-CSF was administered at 5 ug/kg/day on days-17 to -10. When white blood cell is more than 20G/L, stop using G-CSF.
DRUGDecitabine (DAC)Decitabine was administered at 20mg/m2/day on days -14 to -10.
DRUGBusulfanBusulfan was administered at 3.2 mg/kg/day on days -7 to -4 in G-CSF+DAC+BUCY group.
DRUGFludarabine (FLU)Fludarabine was administered at 30 mg/m2/day on days -7 to -3.
DRUGCyclophosphamide (CY)Cyclophosphamide was administered at 60 mg/kg/day on days -3,-2.
DRUGBusulfan (BU)Busulfan was administered at 3.2 mg/kg/day on days -6 to -3 in G-CSF+DAC +BF group.

Timeline

Start date
2022-07-01
Primary completion
2023-12-01
Completion
2024-12-01
First posted
2022-07-12
Last updated
2023-03-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05453552. Inclusion in this directory is not an endorsement.