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- W3202198377 abstract "Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders with heterogeneous presentation, ranging from indolent disease courses to aggressive diseases similar to acute myeloid leukemia (AML). Approximately 90% of MDS patients harbor recurrent mutations , which - with the exception of mutated SF3B1 -have not (yet) been included into the diagnostic criteria or risk stratification for MDS. Accumulating evidence suggests their utility for diagnostic workup, treatment indication and prognosis. Subsequently, in patients with unexplained cytopenia or dysplasia identification of these mutations may lead to earlier diagnosis. The acquisition and expansion of additional driver mutations usually antecedes further disease progression to higher risk MDS or secondary AML and thus, can be clinically helpful to detect individuals that may benefit from aggressive treatment approaches. Here, we review our current understanding of somatic gene mutations, gene expression patterns and flow cytometry regarding their relevance for disease evolution from pre-neoplastic states to MDS and potentially AML." @default.
- W3202198377 created "2021-10-11" @default.
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- W3202198377 date "2021-11-01" @default.
- W3202198377 modified "2023-10-05" @default.
- W3202198377 title "Myelodysplastic syndromes: Biological and therapeutic consequences of the evolving molecular aberrations landscape" @default.
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- W3202198377 doi "https://doi.org/10.1016/j.neo.2021.09.002" @default.
- W3202198377 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8495032" @default.
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