Venetoclax Resistance in Acute Myeloid Leukemia.
Sylvain GarciazMarie-Anne HospitalYves ColletteNorbert VeyPublished in: Cancers (2024)
Venetoclax is a BH3-mimetics agent interacting with the anti-apoptotic protein BCL2, facilitating cytochrome c release from mitochondria, subsequent caspases activation, and cell death. Venetoclax combined with azacitidine (VEN-AZA) has become a new standard treatment for AML patients unfit for intensive chemotherapy. In the phase III VIALE-A study, VEN-AZA showed a 65% overall response rate and 14.7 months overall survival in comparison with 22% and 8 months in the azacitidine monotherapy control arm. Despite these promising results, relapses and primary resistance to venetoclax are frequent and remain an unmet clinical need. Clinical and preclinical studies have been conducted to identify factors driving resistance. Among them, the most documented are molecular alterations including IDH , FLT3 , TP53 , and the newly described BAX mutations. Several non-genetic factors are also described such as metabolic plasticity, changes in anti-apoptotic protein expression, and dependencies, as well as monocytic differentiation status. Strategies to overcome venetoclax resistance are being developed in clinical trials, including triplet therapies with targeted agents targeting IDH, FLT3, as well as the recently developed menin inhibitors or immunotherapies such as antibody-drug conjugated or monoclonal antibodies. A better understanding of the molecular factors driving venetoclax resistance by single-cell analyses will help the discovery of new therapeutic strategies in the future.
Keyphrases
- cell death
- acute myeloid leukemia
- chronic lymphocytic leukemia
- clinical trial
- phase iii
- single cell
- open label
- end stage renal disease
- tyrosine kinase
- ejection fraction
- small molecule
- high throughput
- chronic kidney disease
- cancer therapy
- allogeneic hematopoietic stem cell transplantation
- stem cells
- radiation therapy
- acute lymphoblastic leukemia
- current status
- prognostic factors
- photodynamic therapy
- cell proliferation
- cell cycle arrest
- squamous cell carcinoma
- low grade
- drug delivery
- double blind
- peritoneal dialysis
- anti inflammatory
- bone marrow
- binding protein
- signaling pathway
- amino acid
- quantum dots
- clinical evaluation