Shanghai General Hospital
Shanghai, China
Location status: Recruiting
NCT Number: NCT06686108
This study is a prospective, phase II clinical trial with the primary objective of assessing the effectiveness of demethylating agents combined with venetoclax in the prevention of recurrence after allogeneic hematopoietic stem cell transplantation (allo-HSCT) of high risk T-lymphoblastic lymphoma/leukemia (T-LBL/ALL) patients.
Interested in participating?
Request Info14 year–55 year
All sexes
Interventional
Phase 2
Shanghai, China
Location status: Recruiting
The experimental group included high risk T-ALL/LBL patients after allo-HSCT, who received relapse prevention treatment with demethylating agents such as azacitidine or decitabine, combined with venetoclax.
The historical control consisted of high-risk T-ALL/LBL patients who received allo-HSCT but did not receive any prophylactic treatment from multiple centers, and their basic information, disease information, treatment details, and efficacy data were collected. Propensity score matching was conducted with historical data to compare the advantages and disadvantages of the experimental regimen with the control group.
The primary endpoint was the relapse-free survival(RFS) rate after prophylaxis, while secondary endpoints included cumulative incidence of relapse (CIR), overall survival (OS), and the GVHD-relapse-free survival (GRFS). This study aims to provide a effective and safer prophylaxis treatment for high-risk T-LBL/ALL patients after all-HSCT.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
:
Azacitidine, ih, 32mg/m2/d, days 1-5 of each 28-day cycle
decitabine, 5mg/m2/d, days 1-5 of each 28-day cycle.
venetoclax, 400mg/d, days 1-7 of each 28-day cycle
Time frame: 1 year
1-year relapse-free survival
Time frame: 2 year
2-year relapse-free survival
Time frame: 1 year
1-year cumulative incidence of relapse
Time frame: 2 year
2-year cumulative incidence of relapse
Time frame: 1 year
1-year overall survival
Time frame: 2 year
2-year overall survival
Time frame: 1 year
1-year graft-versus-host disease (GVHD)-free/relapse-free survival (GRFS) rates
Time frame: 2 year
2-year graft-versus-host disease (GVHD)-free/relapse-free survival (GRFS) rates
Time frame: 1 year
1-year cumulative incidence of cGVHD
Time frame: 2 year
2-year cumulative incidence of cGVHD
Time frame: at the end of every cycle (each cycle is 28 days)
adverse events during research
Contact information is provided by the study sponsor or research team.
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Other
Safety and Efficacy Study of Demethylating Agents With Venetoclax in Preventing Recurrence of High-risk T-cell Lymphoblastic Lymphoma/Leukemia After Transplantation
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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