Actively Recruiting
A Single-arm, Prospective Study of TBI + BUMEL As a Conditioning Regimen for Salvage HSCT in Patients with R/R AML
Led by The First Affiliated Hospital of Soochow University · Updated on 2025-03-17
40
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Acute myeloid leukemia (AML) is one of the hematologic malignancies, for which patients typically undergo chemotherapy to achieve complete remission. However, approximately 30% of patients fail to respond to initial treatment, and many experience relapse after achieving remission. For patients with relapsed or refractory AML, allogeneic hematopoietic stem cell transplantation (HSCT) offers a potentially curative option. Sibling-matched HSCT has demonstrated a disease-free survival rate of 20-30%, while unrelated donor transplants yield an overall survival rate of approximately 22%. Haploidentical transplantation is a viable alternative for patients lacking a sibling donor. A 2019 study involving 1,693 patients with relapsed/refractory (R/R) AML revealed that haploidentical transplants yielded outcomes comparable to other transplant modalities, including HLA-matched and 9/10 matched unrelated donor transplants, thus supporting haploidentical transplantation as a viable therapeutic option. The conditioning regimen is a critical component of the transplantation. In China, the modified BU/CY conditioning regimen, which combines busulfan (BU) and cyclophosphamide (CTX), is widely utilized for tumor cytoreduction and immunosuppression. Some centers also employ post-transplant cyclophosphamide (PTCy) to mitigate the risk of graft-versus-host disease (GVHD). Despite advances, relapse remains a significant challenge. Optimizing conditioning regimens to enhance tumor cell targeting and achieve deeper remission is crucial. Additionally, many patients are unfit due to prior chemotherapy, infections, and organ dysfunction, which may make them unable to tolerate high-intensity conditioning. Recent studies suggest that melphalan (MEL)-based conditioning regimens may offer advantages over CTX-based protocols. While total body irradiation (TBI) has been traditionally used in conditioning for HSCT, it is associated with considerable organ toxicity. A low-dose TBI regimen combined with BU+MEL represents a promising conditioning regimen for R/R AML. In preliminary studies, 7 patients treated with this regimen successfully achieved hematopoietic stem cell engraftment. Building on these results, a clinical study is planned to evaluate further the safety and efficacy of the TBI+BUMEL (IBM) conditioning regimen in relapsed/refractory AML, with a focus on improving engraftment rates, reducing relapse rates, minimizing GVHD incidence, and enhancing overall survival outcomes.
CONDITIONS
Official Title
A Single-arm, Prospective Study of TBI + BUMEL As a Conditioning Regimen for Salvage HSCT in Patients with R/R AML
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 14 and 70 years (inclusive)
- Diagnosis of relapsed or refractory AML according to WHO 2016 criteria
- Relapsed AML defined as leukemic cells reappearing after remission or extramedullary leukemic infiltration
- Refractory AML defined as no response to two standard treatments or multiple relapses
- Liver enzymes ALT and AST no more than 3 times the upper normal limit
- Total bilirubin no more than 3 times the upper normal limit
- Serum creatinine no more than 2 times the upper normal limit or creatinine clearance at least 40 mL/min
- Left ventricular ejection fraction above 50% measured by echocardiography or MUGA scan
- Availability of a suitable allogeneic donor
- Life expectancy of at least 3 months
- Karnofsky Performance Status at least 60% and ECOG performance status 0 to 2
- Ability to understand and voluntarily sign informed consent form
You will not qualify if you...
- History of serious allergic reactions to investigational drugs
- History of immunodeficiency or organ transplantation
- Recent severe cardiovascular events within 6 months such as hypertension, arrhythmia, heart failure, or stroke
- Surgery of Class II or higher within 4 weeks before enrollment
- Active, difficult-to-control infections including HIV or hepatitis B or C
- Active central nervous system leukemia involvement
- Pregnant or lactating
- Participation in other clinical studies
- Any other condition deemed unsuitable by the investigator
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hematology Department, The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China, 215006
Actively Recruiting
Research Team
X
Xiaojin Wu, Prof.
CONTACT
D
Depei Wu, Prof.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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