Overview
Very high-risk acute lymphoblastic leukemia
Description
- Arm A : Philadelphia chromosome-positive : Induction (Except Consolidation #3 using
Blinatumomab, all administration should be given with Dasatinib.)
- Morphologic Complete Remission after the Induction : Consolidation #1 →
Consolidation #2 → Consolidation #3
- If Minimal Residual Disease & qPCR not detected after the post-consolidation #1 : Consolidation #3 using High Dose Methotrexate, High Dose Cytarabine → DI(Delayed Intensification) #1 → IM(Interim Maintenance) #2 → DI(Delayed Intensification) #2 → Maintenance
- If Minimal Residual Disease or qPCR(Quantitative Polymerase Chain Reaction) positivie after the post-consolidation #1 : Consolidation #3 using Blinatumomab →Allogeneic HSCT(Hematopoietic Stem Cell Transplantation)
- M2 or M3 after the Induction : Re-induction → Consolidation #2 → Consolidation
#3 → Allogeneic HSCT(Hematopoietic Stem Cell Transplantation)
- If Minimal Residual Disease & qPCR(Quantitative Polymerase Chain Reaction) not detected after the post-consolidation #1 : Consolidation #3 using High Dose Methotrexate, HD Cytarabine
- If Minimal Residual Disease or qPCR(Quantitative Polymerase Chain Reaction) positivie after the post-reinduction : Consolidation #3 using Blinatumomab
- In Arm A, except Consolidation #3 using Blinatumomab, all administration should be given with Dasatinib.
- Arm B : Other VHR ALL except Philadelphia chromosome-positive : Induction
- Morphologic Complete Remission after the Induction : Consolidation #1 →
Consolidation #2 → Consolidation #3
- If Minimal Residual Disease not detected after the post-consolidation #1 : Consolidation #3 using High Dose Methotrexate, High Dose Cytarabine → Allogeneic HSCT(Hematopoietic Stem Cell Transplantation)
- If Minimal Residual Disease positivie after the post-consolidation #1 : Consolidation #3 using Blinatumomab →Allogeneic HSCT(Hematopoietic Stem Cell Transplantation)
- M2 or M3 after the Induction : Re-induction → Consolidation #2 → Consolidation
#3 → Allogeneic HSCT(Hematopoietic Stem Cell Transplantation)
- If Minimal Residual Disease not detected after the post-consolidation #1 : Consolidation #3 using High Dose Methotrexate, High Dose Cytarabine
- If Minimal Residual Disease positivie after the post-reinduction : Consolidation #3 using Blinatumomab
- Morphologic Complete Remission after the Induction : Consolidation #1 →
Consolidation #2 → Consolidation #3
Eligibility
Inclusion Criteria:
- Pediatric patients diagnosed with ALL between the ages of 1 and 19 years at the time
of diagnosis who meet one or more of the following conditions:
- Philadelphia chromosome-positive t(9;22)(q34;q11) or
- Patients with failed remission who had blast > 5% on bone marrow test after initial remission induction therapy or
- Hypodiploidy (Number of chromosomes < 44 (less than 44)) or
- E2A-HLF(Hepatic Leukemia Factor) translocation-positive or
- When the prognosis is judged to be poor according to NGS-MRD results among high-risk ALL patients (i) In B-ALL, the NGS-MRD(Next Generation Sequencing-Minimal Residual Disease) after consolidation therapy is 0.01% or more, and the NGS-MRD followed during interim maintenance treatment is also 0.01% or more, (ii) In T-ALL, NGS-MRD(Next Generation Sequencing-Minimal Residual Disease) is more than 0.01% after consolidation therapy
Exclusion Criteria:
- Participants with contraindications to medications
- When the study participant or their legal representative withdraws consent
- Pregnant or lactating women (patients of child-bearing potential require adequate contraception during the study period)
- Participants who are medically unsuitable to participate in this study at the discretion of the investigator Participants participating in other interventional studies other than this protocol