Azacitidine and Venetoclax in Treating Patients with Acute Myeloid Leukemia in Remission
This phase II trial studies how well azacitidine and venetoclax work in treating patients with acute myeloid leukemia that is in remission. Drugs used in chemotherapy, such as azacitidine and venetoclax, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
Inclusion Criteria
- Patients aged >/= 18 years AML who have achieved their FIRST complete remission (CR) or complete remission with incomplete count recovery (CRi) and are not immediately candidates for allogeneic stem cell transplant.
- Patients who have received intensive therapy (defined as receiving standard or higher dose cytarabine-based therapy) to achieve remission (CR/CRi) should have received remission induction therapy and at least 1 consolidation cycle. These patients are eligible as long as they are not greater than 2 months from their last consolidation therapy and will be enrolled in COHORT 1.
- Patients who have received lower intensity therapy (defined as receiving low-dose cytarabine [LDAC] or hypomethylating agent [HMA]-based therapy) to achieve remission should have received at least 2 cycles of lower intensity therapy between the time they have achieved CR/CRi and enrollment on this protocol. They will be treated on COHORT 2. – Closed to enrollment following institutional review board (IRB) approval of amendment version 7.
- For either subgroup (lower or higher intensity), patients who have measurable residual disease may be enrolled on their respective cohort at any time without maximum ‘time from consolidation’ requirement.
- Eastern Cooperative Oncology Group (ECOG) performance status of < or = 3.
- Serum total bilirubin < or = to 1.5 x the upper limit of normal (ULN).
- Serum creatinine < or = to 2.5 x ULN.
- Absolute neutrophil count (ANC) > 0.5 x k/mcgL.
- Platelet count > or = 30 x k/mgcL.
- For females of childbearing age, they may participate if they: * Have a negative serum or urine pregnancy test within 10 to 14 days of enrolling. * Agree to either abstinence or 2 effective contraceptive methods throughout the treatment period and up to 30 days after discontinuing treatment.
- For male patients with a female partner of childbearing age, they may participate if they agree to either abstinence or 2 effective contraceptive methods throughout the treatment period and up to 30 days after discontinuing treatment.
- Ability to understand and sign informed consent.
Exclusion Criteria
- Diagnosis of acute promyelocytic leukemia (APL), AML - M3 by FAB classification based on morphology, immunophenotype, molecular, or cytogenetics studies.
- Diagnosis of AML associated t(15;17) or APL variant. Patients with t(9;22) are also ineligible unless they are unable or unwilling to receive therapy with a tyrosine kinase inhibitor.
- Uncontrolled intercurrent illness including, but not limited to active uncontrolled infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Patients with active central nervous system (CNS) disease.
- Patients with documented hypersensitivity to any components of the study program.
- Females who are pregnant or lactating or intending to become pregnant during the study.
- Patients with history of extramedullary AML, except for CNS involvement that is currently controlled, will not be eligible for enrollment.
- Patient should be removed from current trial if they wish to participate and get treatment on another trial.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT04062266.
PRIMARY OBJECTIVE:
I. To assess relapse-free survival (RFS) of patients with acute myeloid leukemia (AML) treated with 5-azacytidine (azacitidine; AZA) combined with venetoclax (VEN) as maintenance therapy after achieving remission.
SECONDARY OBJECTIVES:
I. To assess modified RFS of patients with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.
II. To assess overall survival (OS) of patients with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.
III. To assess event-free survival (EFS) of patients with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.
IV. To assess the duration of remission (CRd) of patients with AML treated 5-azacytidine combined with venetoclax as maintenance therapy.
V. To assess toxicity and safety of 5-azacytidine combined with venetoclax as maintenance therapy in patients with AML.
VI. To assess the effects of 5-azacytidine combined with venetoclax on dynamics of minimal residual disease (MRD) and their relationship to outcomes.
VII. To assess the feasibility of maintenance therapy with 5-azacytidine combined with venetoclax in patients with AML who have achieved a remission.
OUTLINE:
Patients receive azacitidine subcutaneously (SC) or intravenously (IV) over 1 hour daily on days 1-5, and venetoclax orally (PO) daily on days 1-14. Treatment repeats every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and/ or biopsy and blood sample collection on study.
After completion of study treatment, patients are followed up at 30 days and then every 6-12 months thereafter.
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationM D Anderson Cancer Center
Principal InvestigatorTapan M. Kadia
- Primary ID2019-0226
- Secondary IDsNCI-2019-04987
- ClinicalTrials.gov IDNCT04062266