ASH 2013
7. bis 10. Dezember, New Orleans
Neue Behandlungsmöglichkeiten des multiplen Myeloms
ASH 2013: Myelodysplastische Syndrome – quo vadis?
Neues zur Behandlung lymphatischer B-Zell-Neoplasien
Schlüsselwörter: Adriamycin, Afuresertib, alkylierende Substanzen, Arry-520, ASH, Azacitidin, Bortezomib, Brentuximab-Vedotin, Bruton-Tyrosinkinase, BTK, Chlorambucil, CLL, Cohesin-Mutationen, CXCR4-Antagonisten, Cyclophosphamid, Cytarabin, Decitabin, Deletion 5q, Dexa-BEAM, Dexamethason, Elotuzumab, Filanesib, Fludarabin, Hodgkin-Lymphom, Hypomethylierende Substanzen, Idelalisib, Immunmodulatoren, Indatuximab, Ixazomib, JAK/STAT, Lenalidomid, LGH447, Maligne Lymphome, Mantelzell-Lymphom, MDS, Melphalan, Milz-Tyrosinkinase, MM, MOR202, Multiples Myelom, Myelodysplastische Syndrome, New Orleans, NFκB, NHL, Non Hodgkin-Lymphom, Obinutuzumab, Ofatumumab, Panobinostat, PI3K, Pomalidomid, Prednison, Proteasominhibitoren, Ravtansin, R-CHOP, R-DHAP, R-ICE, Rituximab, RNA-Helicase, Rocilinostat , SAR650984, Stammzelltransplantation, Thalidomid, Veliparib, Vincristin, Vorinostat