Advances in the management of higher-risk myelodysplastic syndromes: future prospects.
Georgina Gener-RicosJuan José Rodríguez SevillaSamuel UrrutiaAlex BatallerAlexandre BazinetGuillermo Garcia-ManeroPublished in: Leukemia & lymphoma (2024)
Higher-risk myelodysplastic syndromes (HR-MDS) are defined using a number of prognostic scoring systems that include the degree of cytopenias, percentage of blasts, cytogenetic alterations, and more recently genomic data. HR-MDS encompasses characteristics such as progressive cytopenias, increased bone marrow blasts, unfavorable cytogenetics, and an adverse mutational profile. Survival is generally poor, and patients require therapy to improve outcomes. Hypomethylating agents (HMAs), such as azacitidine, decitabine, and more recently, oral decitabine/cedazuridine, are the only approved therapies for HR-MDS. These are often continued until loss of response, progression, or unacceptable toxicity. Combinations including an HMA plus other drugs have been investigated but have not demonstrated better outcomes compared to single-agent HMA. Moreover, in a disease of high genomic complexity such as HR-MDS, therapy targeting specific genomic abnormalities is of interest. This review will examine the biological underpinnings of HR-MDS, its therapeutic landscape in the frontline and relapsed settings, as well as the impact of hematopoietic stem cell transplantation, the only known curative intervention for this disease.
Keyphrases
- acute myeloid leukemia
- bone marrow
- end stage renal disease
- copy number
- prognostic factors
- ejection fraction
- randomized controlled trial
- chronic kidney disease
- multiple sclerosis
- current status
- acute lymphoblastic leukemia
- mesenchymal stem cells
- emergency department
- peritoneal dialysis
- machine learning
- single cell
- electronic health record
- gene expression
- type diabetes
- cancer therapy
- insulin resistance
- metabolic syndrome
- patient reported outcomes
- weight loss
- adipose tissue
- big data
- rectal cancer
- cell therapy
- genome wide
- patient reported
- adverse drug