Table 1.

Prognostic systems proposed for patients with myelodysplastic syndromes.

Stated Major Components of Prognostic System
Prognostic systemPt. PSPt. AgeHb. or Transf.WBC/ANCPlt.LDHBlood blastsMarrow blastsMarrow morphology*Cyto-geneticsFAB classificationWHO classificationFirst AuthorJournal/Year Published
* Includes abnormal localization of immature precursors (ALIP), marrow fibrosis, marrow cellularity, myeloid:erythroid ratio, or cellular dysplasia. 
Comments: The list of prognostic systems excludes systems proposed specifically for chronic myelomonocytic leukemia (CMML), such as the modified Bournemouth score and the MD Anderson CMML proposal, since CMML is classified separately from MDS by the WHO. 
Note that some columns are not entirely independent of others; for instance, blood counts and marrow and blood blast proportion contribute to the WHO classification. 
IPSS indicates International Prognostic Scoring System; WPSS, WHO-based Prognostic Scoring System; MDACC, MD Anderson Cancer Center; Pt., patient; PS, performance status; Hb., hemoglobin; WBC, white blood count; ANC, absolute neutrophil count; Plt, platelet count; LDH, lactate dehydrogenase; Trans., transfusion requirement; Cytogen, cytogenetic results (either complexity, specific abnormalities, or proportion of abnormal metaphases); FAB, French-American-British classification; class., classification. 
Bournemouth         Mufti Br J Haem 1985 
Dutch         Kerkhofs Br J Haem 1987 
Sanz (Spanish)        Sanz Blood 1989 
Pavia          Cassano Haematologica 1990 
Rennes “3-D”          Goasquen Leuk Res 1990 
Düsseldorf         Aul Leukemia 1992 
Japanese        Toyama Leukemia 1993 
Hannover Histopathology          Maschek Eur J Haem 1994 
Lille       Morel Leukemia 1996 
IPSS       Greenberg Blood 1997 
WPSS          Malcovati J Clin Onc 2007 
MDACC (Lower-risk)        Garcia-Manero Leukemia 2008 
MDACC (General)      Kantarjian Cancer 2008 
Modified WPSS         Della Porta Haematologica 2009 
Stated Major Components of Prognostic System
Prognostic systemPt. PSPt. AgeHb. or Transf.WBC/ANCPlt.LDHBlood blastsMarrow blastsMarrow morphology*Cyto-geneticsFAB classificationWHO classificationFirst AuthorJournal/Year Published
* Includes abnormal localization of immature precursors (ALIP), marrow fibrosis, marrow cellularity, myeloid:erythroid ratio, or cellular dysplasia. 
Comments: The list of prognostic systems excludes systems proposed specifically for chronic myelomonocytic leukemia (CMML), such as the modified Bournemouth score and the MD Anderson CMML proposal, since CMML is classified separately from MDS by the WHO. 
Note that some columns are not entirely independent of others; for instance, blood counts and marrow and blood blast proportion contribute to the WHO classification. 
IPSS indicates International Prognostic Scoring System; WPSS, WHO-based Prognostic Scoring System; MDACC, MD Anderson Cancer Center; Pt., patient; PS, performance status; Hb., hemoglobin; WBC, white blood count; ANC, absolute neutrophil count; Plt, platelet count; LDH, lactate dehydrogenase; Trans., transfusion requirement; Cytogen, cytogenetic results (either complexity, specific abnormalities, or proportion of abnormal metaphases); FAB, French-American-British classification; class., classification. 
Bournemouth         Mufti Br J Haem 1985 
Dutch         Kerkhofs Br J Haem 1987 
Sanz (Spanish)        Sanz Blood 1989 
Pavia          Cassano Haematologica 1990 
Rennes “3-D”          Goasquen Leuk Res 1990 
Düsseldorf         Aul Leukemia 1992 
Japanese        Toyama Leukemia 1993 
Hannover Histopathology          Maschek Eur J Haem 1994 
Lille       Morel Leukemia 1996 
IPSS       Greenberg Blood 1997 
WPSS          Malcovati J Clin Onc 2007 
MDACC (Lower-risk)        Garcia-Manero Leukemia 2008 
MDACC (General)      Kantarjian Cancer 2008 
Modified WPSS         Della Porta Haematologica 2009 
Close Modal

or Create an Account

Close Modal
Close Modal