AML (Acute Myelogenous Leukemia)
Conditions
Brief summary
This is a single-center, prospective, single-arm, exploratory clinical study. To explore the efficacy and safety of avapritinib in patients with recurrent acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation with C-KIT mutation RUNX1::RUNX1T1 or CBFB::MYH11.
Detailed description
We enrolled 20 patients with recurrent acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation of RUNX1::RUNX1T1 or CBFB::MYH11 with C-KIT mutation. The study was divided into induction therapy period and consolidation therapy period, and the study design was as follows: A: Induction therapy period: After patients were screened and enrolled, they began to receive 1-2 cycles of induction therapy, and the specific administration regimen was as follows: Avapritinib 100mg po qd D1-D14, azacitidine 35mg/m2 ih D1-D5, Venetoclax 100mg po qd D1-D14. The 28-day cycle was followed by curative effect evaluation at the end of each cycle. Patients who achieved complete remission entered the consolidation treatment stage. B: Consolidation therapy period: Patients who achieved complete remission after 1-2 cycles of induction therapy continued to receive avapritinib 100mg/d po. monotherapy for consolidation therapy, with a cycle of 28 days and a total of 4 cycles.
Interventions
DRUGAvapritinib, azacitidine, Venetoclax
A: Induction therapy period: After patients were screened and enrolled, they began to receive 1-2 cycles of induction therapy, and the specific administration regimen was as follows: Avapritinib 100mg po qd D1-D14, azacitidine 35mg/m2 ih D1-D5, Venetoclax 100mg po qd D1-D14. The 28-day cycle was followed by curative effect evaluation at the end of each cycle. Patients who achieved complete remission entered the consolidation treatment stage. B: Consolidation therapy period: Patients who achieved complete remission after 1-2 cycles of induction therapy continued to receive avapritinib 100mg/d po. monotherapy for consolidation therapy, with a cycle of 28 days and a total of 4 cycles
Sponsors
Institute of Hematology & Blood Diseases Hospital, China
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Subjects met the criteria for recurrence after allogeneic transplantation: re-emergence of leukemia cells or bone marrow original cells in peripheral blood \>5% (except for other causes such as bone marrow recovery period) or extramedullary leukemia cell infiltration or molecular or cytogenetic recurrence. 2. Bone marrow molecular biology detected C-KIT D816 or C-KIT N822 mutations 3. Patients with CBFB::MYH11 gene or RUNX1::RUNX1T1 fusion gene detected. 4. Eastern Cancer Collaboration Group (ECOG) physical status score 0-2 points. 5. Liver, kidney and cardiopulmonary functions met the following requirements: Within 2 weeks before enrollment ① creatinine ≤1.5 upper limit of normal value; ② Left ventricular ejection fraction ≥50%; ③ Blood oxygen saturation \>91%; ④ Total bilirubin ≤2×ULN; ALT and AST≤2.5 x ULN; Myocardial enzymes \< 2 times the upper limit of normal (for the same age) 6. Volunteer to participate in clinical studies and sign informed consent, willing to follow and able to complete all trial procedures.
Exclusion criteria
1. Known allergy to KIT inhibitor drug analogues. 2. Patients who have received previous treatment with Midostaurin. 3. Patients who have previously been treated with mutation-specific C-KIT inhibitors and have developed disease progression during treatment. 4. FLT3-ITD mutation in patients with recurrent/refractory disease (except low gene ratio). 5. HIV infected persons, HBV, HCV active infected persons. 6. Accompanied by uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, serious infectious diseases and other diseases. 7. With uncontrolled active GVHD (NIH for GVHD diagnosis and classification standards, aGVHD classification refer to the improved Glucksberg standard). 8. Central nervous system leukemia.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 2-month ORR after induction therapy | 2 months after induction therapy | 2-month objective remission rate after induction therapy |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| CR rate after induction therapy | 2 months after induction therapy | CR rate after 2 months |
| MRD negative rate after induction therapy | 2 months after induction therapy | MRD negative rate after 2 months |
| Response rate after Consolidation treatment | 6 months after Consolidation treatment | Response rate after 6 months |
| Safety | 2 years | Types of adverse events (AE), AE severity, Relevance to study drugs |
Countries
China
Contacts
Primary ContactErlie Jiang
Backup ContactYigeng Cao
Outcome results
None listed