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This is a prospective, single-center, observational study to evaluate the efficacy and safety of salvage haploidentical allogeneic hematopoietic stem cell transplantation (haplo-HSCT) combined with post-transplant relapse prevention strategies in patients with relapsed/refractory acute myeloid leukemia (R/R AML).
Eligible patients are adults aged 18-65 years with active AML (bone marrow blasts >5% or extramedullary disease) and HCT-CI score ≤5. All patients will receive a uniform conditioning regimen consisting of fludarabine, busulfan, and MECCNU, with addition of targeted agents (such as sorafenib, midostaurin, or venetoclax) according to mutation status. Graft-versus-host disease (GVHD) prophylaxis includes reduced-dose ATG (6 mg/kg), FK506, MMF, and basiliximab. Post-transplant maintenance with targeted therapy or azacitidine and prophylactic donor lymphocyte infusion (DLI) will be administered to reduce relapse risk.
The primary endpoints are cumulative incidence of relapse (CIR), overall survival (OS), and progression-free survival (PFS). Secondary endpoints include incidence of acute and chronic GVHD, CMV/EBV reactivation, non-relapse mortality (NRM), and GVHD-free, relapse-free survival. Patients will be followed for 24 months after transplantation. This study aims to explore an optimized transplant strategy to improve long-term survival in this high-risk population.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Salvage Haploidentical HSCT Cohort | Patients with relapsed/refractory acute myeloid leukemia (R/R AML) who have active disease (bone marrow blasts >5% or extramedullary involvement) before transplantation, aged 18-65 years, and HCT-CI score ≤5. All patients in this single-arm prospective observational cohort will receive salvage haploidentical allogeneic hematopoietic stem cell transplantation (haplo-HSCT) followed by standardized post-transplant relapse prevention strategies. Participants will be followed for 24 months after transplantation. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (haplo-HSCT) | Procedure | Salvage haploidentical allogeneic hematopoietic stem cell transplantation using a conditioning regimen of Fludarabine (120-180 mg/m²), Busulfan (3-4 mg/kg), and MECCNU 250 mg/m² (intensity adjusted based on prognostic index). Targeted agents (sorafenib, midostaurin, or venetoclax) are added according to genetic mutations (e.g., FLT3) until stem cell infusion. GVHD prophylaxis includes ATG 6 mg/kg, tacrolimus (FK506), mycophenolate mofetil (MMF), and basiliximab on day +4. No MTX or post-transplant cyclophosphamide (PTCY) is used. Immunosuppressants are tapered within 100 days if no significant GVHD. |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative Incidence of Relapse (CIR) | Up to 24 months post-transplantation | |
| Overall Survival (OS) | Up to 24 months post-transplantation |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Acute GVHD (aGVHD) | Within 100 days post-transplantation | |
| Incidence of Chronic GVHD (cGVHD) | Up to 24 months post-transplantation |
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Inclusion Criteria:
Exclusion Criteria:
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This is a single-center prospective observational study enrolling adult patients (18-65 years) with relapsed/refractory acute myeloid leukemia (R/R AML) who have active disease (bone marrow blasts >5% or extramedullary involvement) and are scheduled to undergo salvage haploidentical allogeneic hematopoietic stem cell transplantation (haplo-HSCT) at Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. The study population consists of high-risk AML patients with HCT-CI ≤5 who are eligible for intensive transplant therapy according to institutional practice.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| wei MD, PhD | Contact | +86 027-85726003 | shiwei076@hust.edu.cn |
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| Post-transplant Maintenance Therapy | Drug | Starting from approximately day +30 after transplantation, patients receive mutation-guided targeted therapy (sorafenib 200 mg daily for FLT3/ITD mutation) or azacitidine 75 mg/m² on days 1-3. Maintenance therapy aims to reduce the risk of relapse. |
|
| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| D012008 | Recurrence |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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