AI Article Synopsis

  • Patients with lower-risk myelodysplastic syndromes (MDS) mainly suffer from chronic anemia and fatigue, with a focus on improving anemia and reducing the need for blood transfusions.
  • Current treatment options for these patients, especially those without chromosome 5q deletion, are limited, but erythropoiesis-stimulating agents (ESAs) are the first-line therapy showing moderate success for up to two years.
  • Ongoing research is exploring new treatments, like lenalidomide and luspatercept, and aims to enhance therapy effectiveness by integrating genetic data and optimizing patient selection.

Article Abstract

Patients with lower-risk myelodysplastic syndromes (MDS) are affected primarily by symptoms of chronic anemia and fatigue rather than progression to acute myeloid leukemia. Severe thrombocytopenia, although less common in lower-risk MDS, is associated with increased risk of bleeding. For anemic patients, the principal aim of treatment is to improve anemia and decrease red blood cell transfusions. For transfusion-dependent patients with lower-risk MDS without chromosome 5q deletion [non-del(5q) MDS], there are limited effective treatments. Erythropoiesis-stimulating agents (ESAs) are generally first-line therapy, yielding frequent responses with a median duration of 18-24 months. Immunosuppressive therapy or allogeneic stem cell transplantation are restricted to select patients. New strategies for ESA-refractory or relapsed patients include lenalidomide, alone or in combination with ESAs; oral azacitidine; and new molecules such as the activin receptor type II ligand traps luspatercept and sotatercept. In thrombocytopenic patients, thrombopoietin receptor agonists are under evaluation. While trials to evaluate these treatment strategies are underway, efforts are needed to optimize therapies through better patient selection and response prediction as well as integrating molecular and genetic data into clinical practice. We provide an overview of current treatment approaches for lower-risk non-del(5q) MDS and explore promising directions for future research.

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Source
http://dx.doi.org/10.1016/j.leukres.2016.11.008DOI Listing

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