Clinical trial · Interventional
HD-Idarubicin/Etoposide Intensified Conditioning Regimen Allo-HSCT for Adult ALL
An Open-label,Multi-center,Prospective Study of Idarubicin and Etoposide Intensified Conditioning Regimen Allogeneic Hematopoietic Stem Cell Transplantation for Adult Acute Lymphoblastic Leukemia
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Intensified conditioning regimen allo-HSCT is based on a hypothesis of that intensifying condition with less-used drugs could overcome resistance,reduce tumor burden, and most importantly, spare enough time for slow-growing GVL effect following immune reconstitution to finally get rid of MRD and control the disease. Our previous trial of HDE-ALL-2011 (NCT01457040) have confirmed the role of intensified conditioning allo-HSCT in adult ALL, resulting in significantly improved OS and EFS in comparison with previous standard TBI/CY2 conditioning regimen(data not yet published). But at the same time, FA-TBI/CY2-VP16 conditioning regimen was associated with high transplantation-related mortality (TRM), which might be attributed to excessive suppression on both bone marrow and immune. TT-ALL-HIE-2013, substituting FA with idarubicin, is aimed at maintaining anti-tumor effect with less cross-resistance and immune suppression and reducing TRM.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Acute Lymphoblastic Leukemia | Acute Lymphoblastic Leukemia | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CTX | Drug | Cyclophosphamide | ALIAS |
| IDA | Drug | — | UNRESOLVED |
| TBI | Radiation | — | UNRESOLVED |
| VP-16 | Drug | Etoposide | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- IDA-Etoposide Intensified Conditioning
- interventionNames
- Drug: IDA
- Radiation: TBI
- Drug: CTX
- Drug: VP-16
- type
- ACTIVE_COMPARATOR
- label
- Non-IDA Conditioning
- interventionNames
- Radiation: TBI
- Drug: CTX
- Drug: VP-16
Primary outcomes (1)
- measure
- Event-Free Survival
- timeFrame
- 3 year
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 16 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age: 16 years to 65 years; 2. Diagnosis of acute lymphoblastic leukemia; 3. Patient receives allo-HSCT; 4. The informed consent form has been signed; Exclusion Criteria: 1. Patient with severe cardiac dysfunction with less than 50% EF; 2. Patient with severe lung dysfunction; 3. Patient with more than 3 times ULN of serum ALT or AST levels, or with more than 2 times ULN of serum TBIL level, or less than 40% of normal prothrombin time activity (PTA); or with more than 2 times the ULN of serum Cr; 4. Patient with severe active infection; 5. Patient with allergy history about suspected drug in conditioning regimen; 6. Patient with other conditions considered unsuitable for the study.
References
Publications (0)
Data not yet available