Leukemia, Leukemia, Acute, Leukemia, B-cell, Leukemia, Lymphoblastic
Conditions
Keywords
Acute Lymphoblastic Leukemia, Ph-like, Tyrosine Kinase Inhibitor, Histone Deacetylase Inhibitor
Brief summary
Ph-like ALL is a recently recognized high-risk subgroup and the optimal therapeutic approaches are poorly characterized. Based on the pediatric-inspired, PEG-L-asparaginase-intensified and MRD-directed PDT-ALL-2016 protocol, this open-label, two-arm, multi-site trial PDT-Ph-like-ALL is aimed to evaluate the safety and effect of oral histone deacetylase inhibitor chidamide and dasatinib for adult Ph-like ALL.
Detailed description
Ph-like, or BCR-ABL1-like lymphoblastic leukemia is neoplasm of lymphoblasts committed to the B-cell lineage that lack the BCR-ABL1 translocation but show a pattern of the expression very similar to that seen in BCR-ABL1-positive ALL. Chidamide is a novel oral HDACi with promising activity in non-Hodgkin lymphoma (NHL). Based on the pediatric-inspired, PEG-L-asparaginase-intensified and MRD-directed PDT-ALL-2016 protocol, this open-label, two-arm, multi-site trial is aimed to evaluate the safety and effect of oral histone deacetylase inhibitor (HDACi) chidamide and tyrosine kinase inhibitor (TKI) dasatinib for adult Ph-like ALL/LBL. HDACi chidamide and TKI dasatinib will be added to chidamide and dasatinib group, respectively, from induction therapy to consolidation therapy (total courses of chidamide treatment: 5 courses for allo-HSCT after Consolidation Module-3; 12 courses for patients non-allo-HSCT after Consolidation Module 1-9). Primary study endpoint is event-free survival and secondary study endpoints are complete remission and MRD after induction, adverse event and overall survival. Pretreatment: Dexamethasone, -3 to 0d; Chidamide for chidamide arm: 10mg/d, po qd. Dasatinib for Dasatinib arm: 100mg/d, po qd. Induction:VCR: 1, 8, 15, 22; IDA: 1, 8; CTX: 1g/m2, 1; PEG-asp: 2000-2500IU/m2, 1, 15; Pred: 1-24; MRD assessment: d14, 24, 45, and pre-allo-HSCT. VLCAM (MRD1/d14\>1%): CTX, d25; AraC 50mg/m2, d25-31, 26; 6-MP: 25-31, PEG-asp: 26; Consolidation Module: CM1: AraC 2g/m2, q12h, 1-2, Dex: 10mg/m2, 1-2, PEG-asp: 2, 6-MP: 1-7. IT: d1; CM2: MTX 3g/m2, 1, Dex: 10mg/m2, 1-2, PEG-asp: 2; 6-MP: 1-7; IT: d1; CM3: CTX 0.5g/m2, 1-3, PEG-asp: 2, 6-MP: 1-7, IT: d1. Allo-HSCT: after CM3 when donors available. Non-HSCT: finish CM 4-9 and POMP maintenance. CM4-6: repeat CM1-3. Re-Induction: after CM6. CM7-9: repeat CM1-3. Maintenance: POMP-Pred: x12m; VCR x12m; MTX: x24m; 6-MPx24m.
Interventions
Chidamide will be administrated at dose of 10mg/day in chidamide arm in PDT-Ph-Like protocol. PDT-Ph-Like protocol for chidamide arm consists of diagnostic test (bone marrow aspiration, flow immunophenotyping, karyotyping,FISH, NGS, Flow-MRD), induction regimen (chidamide, prednisone, vincristine, cyclophosphamide, idarubicin, pegaspargase), consolidation regimen (chidamide, cytarabine, methotrexate, dexamethasone, cyclophosphamide, etoposide, 6-mercaptopurine, pegaspargase), MRD assessment and maintenance regimen, intrathecal injection chemotherapy, radiation therapy for CNS-involved leukemia and allogeneic hematopoietic stem cell transplantation.
Dasatinib will be administrated at a dose of 100mg/day in dasatinib arm in PDT-Ph-Like protocol. PDT-Ph-Like protocol for dasatinib arm consists of diagnostic test (bone marrow aspiration, flow immunophenotyping, karyotyping,FISH, NGS, Flow-MRD), induction regimen (dasatinib, prednisone, vincristine, cyclophosphamide, idarubicin, pegaspargase), consolidation regimen (dasatinib, cytarabine, methotrexate, dexamethasone, cyclophosphamide, etoposide, 6-mercaptopurine, pegaspargase), MRD assessment and maintenance regimen, intrathecal injection chemotherapy, radiation therapy for CNS-involved leukemia and allogeneic hematopoietic stem cell transplantation.
Sponsors
Study design
Eligibility
Inclusion criteria
* 14-55 years old; * Ph-like ALL newly diagnosed; * signed written informed consent
Exclusion criteria
* Pregnant women; * History of pancreatitis; * History of diabetes; * History of active peptic ulcer disease in the past 6 months; * History of arteriovenous thrombosis in the past 6 months; * Severe active infection; * Allergic to any drugs in PDT-Ph-like-ALL.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Event free survival | 3 years | EFS of Ph-like ALL group |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| CR after Induction Therapy | 3 months | CR rate of Ph-like group |
| Death in induction | 3 months | — |
| Adverse events | 3 years | AE during PDT-Ph-like |
| Minimum residual disease after induction | 3 months | MRD after 1 course |
| Relapse free survival | 3 years | RFS |
| Overall survival | 3 years | OS |
| Relapse | 3 years | Relapse of Ph-like ALL |
Countries
China