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Recruiting NCT06816134

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

Phase II Interventional Acute Myeloid Leukemia Acute Lymphoblastic Leukemia Transplantation, Stem Cell Conditioning Therapy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: TmBU conditioning Regimen, mBUCY conditioning regimen.
Who it may be relevant to
Registry conditions: Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Transplantation, Stem Cell, Conditioning Therapy. Basic parameters: 15 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Prospective, Randomized Controlled Clinical Study on the Efficacy and Safety of the TmBU Regimen Versus mBUCY Regimen for Conditioning Before Allo-HSCT in High-risk or Relapsed/Refractory Acute Leukemia

Overview

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.

Interventions

  • Drug TmBU conditioning Regimen
    TmBU conditioning Regimen and GVHD Prophylaxis of Haploid transplantation (Haplo-HSCT) and unrelated donor transplantation (UDT) : Cyclosporine A (CsA) + Mycophenolate mofetil dispersible tablets (MMF) + short-term low-dose methotrexate (MTX) + rabbit anti-human antithymocyte globulin (ATG) or GVHD Prophylaxis of Matched Sibling Donor Hematopoietic Stem Cell Transplantation (MSD-HSCT)：Cyclosporine A (CsA) + short-term low-dose methotrexate (MTX), then stem cells are infused into patient's blood.
  • Drug mBUCY conditioning regimen
    mBUCY conditioning Regimen and GVHD Prophylaxis of Haploid transplantation (Haplo-HSCT) and unrelated donor transplantation (UDT): Cyclosporine A (CsA) + Mycophenolate mofetil dispersible tablets (MMF) + short-term low-dose methotrexate (MTX) + rabbit anti-human antithymocyte globulin (ATG) or GVHD Prophylaxis of Matched Sibling Donor Hematopoietic Stem Cell Transplantation (MSD-HSCT)：Cyclosporine A (CsA) + short-term low-dose methotrexate (MTX), then stem cells are infused into patient's blood.

Primary outcome measures

  • Cumulative incidence of relapse（CIR） [Time frame: 2 years]
Secondary outcome measures (6)
  • Time period for hematopoietic reconstruction [Time frame: 24 weeks]
  • Incidence of acute graft-versus-host disease (aGVHD) [Time frame: 100 days]
  • Progressing-free survival（PFS） [Time frame: 2 years]
  • Overall survival（OS） [Time frame: 2 years]
  • Non-relapse mortality（NRM） [Time frame: 2 years]
  • Graft-versus-host disease (GVHD)-free relapse-free survival (GRFS) [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • The First Affiliated Hospital of Soochow University — Suzhou

Identifiers

NCT: NCT06816134 · SZConditioning01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗