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• W2101227132 abstract "Allogeneic hematopoietic stem cell transplantation (HSCT) for myelodysplastic syndrome (MDS) is a potentially curative procedure, but is associated with a significant risk of morbidity and mortality. With the recent approval of disease-modifying agents, the appropriate timing of allogeneic HSCT needs to be addressed. Similarly, the optimal use of these disease-modifying agents before HSCT needs to be determined. In severe aplastic anemia, HSCT is a proven cure, but HLA-matched sibling donors are found in fewer than 25% of newly diagnosed patients. The use of early unrelated donor HSCT is an evolving concept that will become more accepted as improvements in HSCT outcomes continue." @default.
• W2101227132 created "2016-06-24" @default.
• W2101227132 creator A5029278364 @default.
• W2101227132 date "2014-12-05" @default.
• W2101227132 modified "2023-10-01" @default.
• W2101227132 title "Timing of allogeneic stem cell transplantation for myelodysplastic syndromes and aplastic anemia" @default.
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• W2101227132 doi "https://doi.org/10.1182/asheducation-2014.1.77" @default.
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