What’s Next after Hypomethylating Agents Failure in Myeloid Neoplasms? A Rational Approach

Author:

Awada Hussein1ORCID,Gurnari Carmelo12ORCID,Xie Zhuoer3,Bewersdorf Jan Philipp4ORCID,Zeidan Amer M.5

Affiliation:

1. Department of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH 44195, USA

2. Department of Biomedicine and Prevention, University of Rome Tor Vergata, 00133 Rome, Italy

3. Department of Hematology, H. Lee Moffitt Cancer Center, Tampa, FL 33612, USA

4. Department of Medicine, Leukemia Service, Memorial Sloan Kettering Comprehensive Cancer Center, New York, NY 10065, USA

5. Section of Hematology, Department of Internal Medicine, Yale University and Yale Cancer Center, New Haven, CT 06511, USA

Abstract

Hypomethylating agents (HMA) such as azacitidine and decitabine are a mainstay in the current management of patients with myelodysplastic syndromes/neoplasms (MDS) and acute myeloid leukemia (AML) as either single agents or in multidrug combinations. Resistance to HMA is not uncommon, and it can result due to several tumor cellular adaptations. Several clinical and genomic factors have been identified as predictors of HMA resistance. However, the management of MDS/AML patients after the failure of HMA remains challenging in the absence of standardized guidelines. Indeed, this is an area of active research with several potential therapeutic agents currently under development, some of which have demonstrated therapeutic potential in early clinical trials, especially in cases with particular mutational characteristics. Here, we review the latest findings and give a rational approach for such a challenging scenario.

Funder

Edward P. Evans Foundation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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