Actively Recruiting
A Single-Arm, Prospective Study of TBI+BUMEL as Conditioning for SCT2 in Patients With Malignant Hematologic Diseases
Led by The First Affiliated Hospital of Soochow University · Updated on 2025-03-13
40
Participants Needed
1
Research Sites
155 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Each year, over 20,000 patients in China undergo hematopoietic stem cell transplantation (HSCT). Unfortunately, the prognosis in patients with disease relapse or graft failure is often inferior. A second allogeneic hematopoietic stem cell transplantation (SCT2) has emerged as a vital salvage therapy option. Despite varying prognoses, most patients undergoing SCT2 have a five-year overall survival (OS) rate of less than 30%. The primary challenges of SCT2 include treatment strategy, immune regulation, complication management, and transplantation technique improvements. By optimizing these key aspects, SCT2 can effectively address issues that arose after the first transplant, reduce complications, and provide more effective treatment for patients. Clinical practice indicates that SCT2 is crucial in treating various hematologic diseases. For patients who failed the first transplant (SCT1), SCT2 can more effectively treat the primary disease, provide timely hematopoietic engraftment, extend survival time, and improve the quality of life. Additionally, the successful application of SCT2 provides clinicians with more treatment options and hope. Currently, the modified BU/CY conditioning regimen, which consists of busulfan (BU) and cyclophosphamide (CY), is commonly used in SCT1 in China. However, for patients who relapse after SCT1, these drugs may become ineffective, and the physical condition often worsens, with a higher likelihood of infections and organ dysfunction. Therefore, finding new conditioning regimens is crucial. Studies have shown that a melphalan (MEL)-based conditioning regimen may have better outcomes for patients with acute myeloid leukemia (AML) compared to a Cy-based regimen. The Conditioning regimen that includes total body irradiation (TBI) has also been considered effective for patients with acute leukemia. Thus, low-dose TBI combined with a BU + MEL regimen could be a promising conditioning regimen for SCT2. In the investigators' preliminary studies, three patients who underwent SCT2 with this regimen successfully achieved engraftment and were discharged. Based on this, the investigators plan to conduct a clinical study to observe the effects of the TBI+BUMEL regimen combined with SCT2 on the engraftment rate, disease relapse rate, GVHD incidence, and survival rate in patients with malignant hematologic diseases who relapsed after SCT1.
CONDITIONS
Official Title
A Single-Arm, Prospective Study of TBI+BUMEL as Conditioning for SCT2 in Patients With Malignant Hematologic Diseases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 14 to 70 years
- Diagnosed with malignant hematologic diseases as defined by WHO criteria
- Indication for second hematopoietic stem cell transplantation after first transplant failure or relapse
- Cardiac, liver, and kidney function within specified laboratory limits
- Having a suitable allogeneic hematopoietic stem cell donor
- Expected survival of at least 3 months
- Karnofsky score of 60% or higher and ECOG status of 2 or less
- Fully understand the study and voluntarily consent to participate
You will not qualify if you...
- History of serious allergic reactions to study drugs
- History of immunodeficiency or organ transplantation
- Recent severe cardiovascular events within the past 6 months
- Major surgery within 4 weeks prior to enrollment
- Active viral infections
- Pregnant or breastfeeding
- Currently enrolled in another clinical trial
- Deemed unsuitable by investigators for any reason
AI-Screening
AI-Powered 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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