Venetoclax and Azacitidine for the Management of Molecular Relapse/Progression in Adult NPM1-mutated Acute Myeloid Leukemia

Gruppo Italiano Malattie EMatologiche dell'Adulto

Status and phase

Enrolling

Phase 2

Conditions

NPM1 Mutation

Acute Myeloid Leukemia, in Relapse

Acute Myeloid Leukemia

Treatments

Drug: Venetoclax+azacitidine

Study type

Interventional

Funder types

Other

Identifiers

NCT04867928

AML2521

Details and patient eligibility

About

This is a phase 2, non-randomized, interventional, open-label, multicenter trial evaluating the efficacy of VEN-AZA as a bridge-to-transplant therapy in chemotherapy-treated adult NPM1mut AML patients who experience molecular relapse or progression during treatment or follow-up. Subjects will receive cycles of venetoclax plus azacitidine. After each cycle, MRD will be evaluated and at any time of MRD-negativity, AlloSCT will be performed.

Full description

Subjects will receive venetoclax 400 mg orally QD on Days 1 - 28 plus azacitidine 75 mg/m2 SC or IV daily for 7 days. Cycle Length: 28 Days.

Subjects will continue treatment until subsequent alloSCT, documented morphological bone marrow and/or extramedullary disease progression, toxicity, withdrawal of consent, or the subject meets other protocol criteria for discontinuation (whichever occurs first).

After each cycle, MRD will be evaluated. AlloSCT is recommended at any time of MRD-negativity. After 6 cycles of treatment, regardless MRD status, patients will proceed to alloSCT.

Enrollment

35 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subject must be ≥ 18 years of age
Subject must have received previous diagnosis of NPM1mut AML with or without concomitant FLT3-TKD or FLT3-ITD
At screening, subject must have confirmed NPM1 type A, B, or D mutant transcripts
Subject must be eligible for alloSCT, according to transplant center policy
Subject must have undergone at least two cycles of conventional anthracycline- and cytarabine-based chemotherapy, achieving first CR (CR1)
Subject must be in morphological CR1 with bone marrow detectable minimal residual disease (MRD) positivity, defined as qRT-PCR NPM1 transcript ≥ 0.01/100 ABL1 copies and confirmed in two consecutive determinations performed at 2 to 4 weeks' distance
1. Molecular progression is defined in patients with molecular persistence at low copy number as an increase of MRD copy number ≥ 1 log10 between 2 positive samples.
2. Molecular relapse is defined in patients previously tested MRD negative as an increase in MRD copy number ≥ 1 log10 between 2 positive samples
Subject must have a projected life expectancy of at least 12 weeks.
Subject must have an Eastern Cooperative Oncology Group (ECOG) Performance status < 2
Subject must have adequate renal and hepatic function per local laboratory reference range as follows:
- Aspartate transaminase (AST) and alanine transaminase (ALT) < 3.0X ULN
- Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin)
- Subject must have adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL/min; calculated by the Cockcroft Gault formula or measured by 24 hours' urine collection.
Female subjects of childbearing potential must have negative results for pregnancy test at screening
Female and male patients who are fertile must agree to use an effective form of contraception with their sexual partners from screening through 3 months after the end of treatment.
Signed written informed consent according to ICH/EU/GCP and national local laws.

Exclusion criteria

Subject has acute promyelocytic leukemia (APL)
Subject has known active CNS involvement with AML
Subject has received previous treatment with venetoclax and/or hypomethylating agents
Subject has undergone alloSCT for AML
Subject has more than 5% of bone marrow blast cells at screening bone marrow aspirate
Subject is known to be positive for HIV
Evidence of other clinically significant uncontrolled condition(s) including, but not limited to:
1. Uncontrolled and/or active systemic infection (viral, bacterial or fungal)
2. Chronic hepatitis B virus (HBV) or hepatitis C (HCV) requiring treatment. Note: subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.
Cardiac history of CHF requiring treatment or Ejection Fraction ≤ 50% or chronic stable angina;
DLCO ≤ 65% or FEV1 ≤ 65%;
Creatinine clearance < 30 ml/min
Subject has a cardiovascular disability status of New York Heart Association Class > 2

a. Class 2 is i. defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity ii. results in fatigue, palpitations, dyspnea, or anginal pain
Patients who are pregnant or breast feeding and adults of reproductive potential not employing an effective method of birth control (women of childbearing potential must have a negative serum pregnancy test within 48 hrs prior to administration of induction therapy). Post-menopausal women must be amenorrhoic for at least 12 months to be considered of non-child bearing potential. Male and female patients must agree to employ an effective barrier method of birth control throughout the study and for up to 3 months following discontinuation of study drugs.
Patients unwilling or unable to comply with the protocol.