Dynamics of Resistance Emergence to Azacitidine-based Therapies in Acute Myeloid Leukemia

Phase

N/A

Condition

Acute Myeloid Leukemia

Leukemia

Platelet Disorders

Treatment

Bone marrow specimens

Biobanking blood

Clinical Study ID

NCT06225128

APHP230805

Ages 18-100
All Genders

Study Summary

Acute myeloid leukemia (AML) is a malignancy of aging endowed with poor prognosis. The combination of the hypomethylating agent azacitidine (AZA) with the BCL-2 inhibitor venetoclax (VEN) is the first-line treatment of older AML patients but is endowed with substantial resistance. The project leverages functional precision oncology, single-cell studies and mouse experiments to dissect the mechanisms of primary and adaptive resistance to AZA/VEN. The primary objective is to prospectively validate an ex vivo drug sensitivity testing (DST) assay as predictor of primary resistance to first-line AZA/VEN in 100 unfit AML patients. The study will also explore whether newer DST assays with enhanced niche mimicry can improve on the standard assay.

By serially interrogating the short-term fate of both leukemic and immune cells upon AZA/VEN exposure in patients primed towards refractoriness, transient or prolonged remission, the aim is to dissect the cell-intrinsic and immune-mediated mechanisms of primary versus adaptive resistance. A parallel flow cytometry study will interrogate the role of senescence in AZA/VEN activity. These translational studies will be mirrored by experiments in a transplantable AML model derived from syngeneic mice harboring the age-related Tet2-/- leukemia-predisposing genotype. Lineage tracing single-cell experiments will backtrack AZA/VEN resistance to determine whether it is driven by selection or adaptation. The actionable stress sensor Pml will be invalidated in the same model to determine whether Pml-driven senescence contributes to AZA/VEN anti-leukemic activity in vivo. The project will pave the way to the clinical implementation of functional precision oncology in a high-risk malignancy. By simultaneously interrogating cell-intrinsic and immune-mediated drug resistance in vivo in a prospective patient cohort mirrored by controlled mice experiments, the project will provide a framework for the integrative analysis of drug resistance in cancers.

Eligibility Criteria

Inclusion

Inclusion Criteria:

be ≥18 years old,
have a newly diagnosed AML according to ICC 2022 criteria,
patients with AML related to prior chemotherapy or radiotherapy for anothercancer will be eligible,
patients with MDS/AML per ICC 2022 criteria will be eligible,
have signed the informed consent form of the eTHEMA observatory trial
have ≥10% blasts on the bone marrow smear at screening,
have not received any treatment for AML except for hydroxyurea and/or steroids,
Patients having previously received hypomethylating agents for an antecedentmyelodysplastic syndrome are ineligible,
be eligible to AZA/VEN or AZA/IVO therapy, due to general health status,
have an ECOG performance status ≤ 2,
be planned to receive azacitidine and venetoclax (AZA/VEN) or azacitidine andivosidenib (AZA/IVO) as frontline therapy,
weigh ≥ 40 kg (compliance to Loi Jardé for PB sampling),
have provided written informed consent obtained prior to any screening procedures

Exclusion

Exclusion Criteria:

At screening, patients must NOT:

have suspected or proven acute promyelocytic leukemia based on morphology, karyotypeor molecular assay, including APL with non-PML::RARA rearrangements,
have suspected or proven AML with t(9;22)(q34.1;q11.2)/BCR::ABL1 based on karyotypeor molecular assay,
have myeloid sarcoma,
have failed to perform bone marrow aspiration at screening,
have received previous therapy for AML with any investigational agent or cytotoxicdrug, within 28 days before starting treatment. Only hydroxyurea is permitted forthe control of blood counts. Aside from hypomethylating agents, other treatments foran antecedent myeloid neoplasm (MDS or MPN) are not considered as exclusioncriteria,
be pregnant or breastfeeding (for women),
present any of concurrent severe and/or uncontrolled medical condition, which couldcompromise participation in the study,
be enrolled in a clinical trial which could compromise participation in the study.

Study Design

Bone marrow specimens

January 16, 2024

June 19, 2027

Connect with a study center

Hôpital Saint Louis
Paris,
France
Active - Recruiting

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