Study on the Efficacy and Safety of the TmBU Conditioning Regimen in High-risk or Relapsed/Refractory Acute Leukemia

Recruiting now · Phase 2

Conditions studied: Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Transplantation, Stem Cell, Conditioning Therapy

In brief

This project is a prospective, single-center, randomized controlled clinical study. The subjects were high-risk or relapsed/refractory AML or ALL patients aged ≤ 65 years diagnosed by bone marrow cell morphology, immunology, genetics and therapeutic efficacy evaluation. The TmBU scheme or modified Bu/Cy (mBuCy) scheme was used for pretreatment in allo-HSCT. The primary endpoint of the study was the 2-year cumulative incidence of relapse (CIR) after allo-HSCT, and the secondary endpoints were 2-year overall survival rate (OS), progressing-free survival rate (PFS), non-relapse mortality rate (NRM), graft-versus-host disease (GVHD)-free relapse-free survival (GRFS) rate.

Key facts

Study ID

NCT06816134

Run by

The First Affiliated Hospital of Soochow University

People needed

48

Starts

2025-01-30

Expected to finish

2030-01-30

Last updated by the study team

2026-04-23

Who can join

Age: 15 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Confirmed diagnosis of AML or ALL according to WHO 2022 guideline criteria, with indications for allo-HSCT list below:
• Relapsed/primary refractory (definitions refer to NCCN 2025) or genetic high-risk group AML at diagnosis (risk stratification refers to ELN 2022)
• High-risk at diagnosis (risk stratification refers to ELN 2022) or MRD positive before transplantation B-ALL
• Confirmed diagnosis of T-ALL
• History of central nervous system leukemia (CNSL) or histopathologically confirmed extramedullary manifestation (EMD) during the course of the AML or ALL
• Age 15-65 years old (≤ 65 years old)
• HCT-CI score < 2 points ECOG 0-2 points
• Adequate organ function:
• Cardiac NYHA grade ≤ 2, left ventricular ejection fraction ≥55%
• Creatinine clearance ≥ 50ml/min
• ALT and AST ≤ 2.5 times the upper limit of the normal range, and total bilirubin ≤ 1.5 times the upper limit of the normal range
• Oxygen saturation > 92% without oxygen
• Expected survival time ≥ 3 months
• Ability to understand and voluntarily sign the informed consent form

You may not qualify if…

• With other malignant tumors and have received any treatment for this tumor within the past 3 years
• Previous or current other CNS disease (such as epilepsy, generalized seizure disorder, paresis, aphasia, stroke, severe brain injuries, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis) or any CNS-related autoimmune disease
• HIV/Syphilis infection or uncontrolled active other infections (bacteria or fungus or virus is included)
• With active hepatitis B or hepatitis C infection
• Patients received cardiac angioplasty or stent implantation within 12 months before signing the informed consent form, or have symptoms requiring medical treatment for coronary heart disease
• With primary immunodeficiency or active autoimmune disease
• Previous history of severe immediate hypersensitivity reactions to any of the drugs to be used in this study
• Received a live vaccine within 6 weeks prior to screening
• Pregnant, lactating females and patients of childbearing potential who are unwilling to use contraception
• Inability to cooperate with the requirements of study, treatment and monitoring due to psychiatric illness or other conditions
• Patients not suitable for the study according to the investigator's assessment

Where it is running

• The First Affiliated Hospital of Soochow University — Suzhou, Jiangsu, China (enrolling)

Full record on ClinicalTrials.gov

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