| Literature DB >> 28189174 |
Abstract
Myelodysplastic syndrome (MDS) is a heterogeneous, clonal stem cell disorder of the blood and marrow typically diagnosed based on the presence of persistent cytopenia(s), dysplastic cells, and genetic markers. Common issues that arise in the clinical management include difficulty confirming MDS diagnosis, lack of a standard approach with novel agents in MDS, and few prospective long-term, randomized controlled MDS clinical studies to guide allogeneic blood and marrow transplant. With the recent genetic characterization of MDS, certain aspects of these issues will be better addressed by integrating genetic data into clinical study design and clinical practice.Entities:
Keywords: Anemia; Azacitidine; Blood and marrow transplant; Myelodysplastic syndrome; Therapy-related myelodysplastic syndrome
Mesh:
Year: 2017 PMID: 28189174 PMCID: PMC5358800 DOI: 10.1016/j.mcna.2016.09.006
Source DB: PubMed Journal: Med Clin North Am ISSN: 0025-7125 Impact factor: 5.456