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10.6004/jnccn.2015.0038

http://scihub22266oqcxt.onion/10.6004/jnccn.2015.0038
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C4696005!4696005 !25736003
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suck abstract from ncbi


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pmid25736003
      J+Natl+Compr+Canc+Netw 2015 ; 13 (3 ): 261-72
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  • Myelodysplastic syndromes, version 2 2015 #MMPMID25736003
  • Greenberg PL ; Stone RM ; Bejar R ; Bennett JM ; Bloomfield CD ; Borate U ; De Castro CM ; Deeg HJ ; DeZern AE ; Fathi AT ; Frankfurt O ; Gaensler K ; Garcia-Manero G ; Griffiths EA ; Head D ; Klimek V ; Komrokji R ; Kujawski LA ; Maness LJ ; O'Donnell MR ; Pollyea DA ; Scott B ; Shami PJ ; Stein BL ; Westervelt P ; Wheeler B ; Shead DA ; Smith C
  • J Natl Compr Canc Netw 2015[Mar]; 13 (3 ): 261-72 PMID25736003 show ga
  • The NCCN Guidelines for Myelodysplastic Syndromes (MDS) comprise a heterogeneous group of myeloid disorders with a highly variable disease course that depends largely on risk factors. Risk evaluation is therefore a critical component of decision-making in the treatment of MDS. The development of newer treatments and the refinement of current treatment modalities are designed to improve patient outcomes and reduce side effects. These NCCN Guidelines Insights focus on the recent updates to the guidelines, which include the incorporation of a revised prognostic scoring system, addition of molecular abnormalities associated with MDS, and refinement of treatment options involving a discussion of cost of care.
  • |Cost-Benefit Analysis [MESH]
  • |Disease Management [MESH]
  • |Genetic Testing [MESH]
  • |Humans [MESH]
  • |Myelodysplastic Syndromes/*diagnosis/genetics/therapy [MESH]


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