Myelodysplastic syndromes have been reclassified by new WHO proposals published in 2008. So far, there are no data on haematological features of the newly composed subtypes. We analyzed 2063 patients with MDS diagnosed according to the WHO 2008 classification. Patients were characterized by their initial haematological features. We especially payed attention towards isolated cytopeniae with regard to the new classification of MDS subcategories. Analyses were performed by the use of the MDS registry Duesseldorf and included hemoglobin level, platelets, leukocytes and karyotype (available in 1091 patients) as well as age, gender, IPSS and WPSS at the time of diagnosis. All items have been assessed in our haematological laboratory and in the department of human genetics, respectively. The table shows characteristic features of MDS patients according to their WHO subtype. The patients’ median age did not differ substantially. There was a preponderance of females in the del(5q), RARS and RC group. Median hemoglobin level ranked lowest in the del(5q) and RAEB II group. Median thrombocyte, leukocyte as well as granulocyte level progressively decreased with more advanced WHO risk groups. Chromosomal aberrations were more frequent with increasing medullary blasts and degree of dysplasia. Likewise, patients with these characteristics were categorized into more advanced WPSS subtypes. About 90% of all patients were anemic, that is patients with a hemoglobin level of under 12 g/dl. Leukocytopenia as well as thrombocytopenia were more severe with increasing medullary blast counts. Of interest, 46% of RC patients showed a leukocytopenia (<4000/μl) and 37% had thrombocytopenia (<150.000/μl). 26% of this group showed an isolated anemia, whereas only 1–3% of the patients presented with an isolated leukocytopenia or thrombocytopenia. The majority of MDS patients presents with bicytopenia, regardless of subtypes. The degree of hematopoietic insufficiency is strongly correlated with the amount of medullary blasts, but as well with the degree of dysplasia in blood and marrow. An inclusion of the number of cytopenia into the WHO classification would lead to an alteration of subcategories and result in a shift towards a higher percentage of multilineage MDS.

RCRARSMDS with del(5q)RCMDRAEB IRAEB II
Frequency  184 162 68 950 306 393 
Age  70 70 64 72 69 67 
Gender (%) 48 48 35 55 58 56 
 52 52 65 45 42 44 
Hemoglobin (g/dl) 9,5 9,5 9,2 9,2 
Thrombocytes (1000/μl) 124 293 284 146 96 80 
Leukocytes (/μl) 4800 5500 4300 3900 3100 2800 
Granulocytes  1950 3200 2400 2200 1400 1200 
Chromosomal Low 70 87 96 63 57 51 
risk by IPSS Intermediate 19 10 18 16 19 
(%) High 11 19 27 30 
Initial IPSS (%) 48 83 72 34 
 42 14 26 53 
 10 13 55 50 
 40 43 
Initial WPSS        
 48 73 40 30 
(%)        
 30 27 60 40 
 22 30 33 
 50 59 
 18 41 
Cytopenia (%) Anemia (<12 g/dl) 85 97 98 89 86 90 
 Leukopenia 46 18 39 50 64 89 
 (<4000/μl)       
 Thrombocytopenia 37 35 52 80 
 (<150.000/μl)       
Isolated (%) Anemia 26 78 51 27 14 
 Leukocytopenia 1,5 
 Thrombocytopenia 
Pancytopenia        
  22 24 35 44 
(%)        
Survival (mths.)  561 69 80 36 19 10 
AML after        
  15 15 32 63 
3 yrs. (%)        
RCRARSMDS with del(5q)RCMDRAEB IRAEB II
Frequency  184 162 68 950 306 393 
Age  70 70 64 72 69 67 
Gender (%) 48 48 35 55 58 56 
 52 52 65 45 42 44 
Hemoglobin (g/dl) 9,5 9,5 9,2 9,2 
Thrombocytes (1000/μl) 124 293 284 146 96 80 
Leukocytes (/μl) 4800 5500 4300 3900 3100 2800 
Granulocytes  1950 3200 2400 2200 1400 1200 
Chromosomal Low 70 87 96 63 57 51 
risk by IPSS Intermediate 19 10 18 16 19 
(%) High 11 19 27 30 
Initial IPSS (%) 48 83 72 34 
 42 14 26 53 
 10 13 55 50 
 40 43 
Initial WPSS        
 48 73 40 30 
(%)        
 30 27 60 40 
 22 30 33 
 50 59 
 18 41 
Cytopenia (%) Anemia (<12 g/dl) 85 97 98 89 86 90 
 Leukopenia 46 18 39 50 64 89 
 (<4000/μl)       
 Thrombocytopenia 37 35 52 80 
 (<150.000/μl)       
Isolated (%) Anemia 26 78 51 27 14 
 Leukocytopenia 1,5 
 Thrombocytopenia 
Pancytopenia        
  22 24 35 44 
(%)        
Survival (mths.)  561 69 80 36 19 10 
AML after        
  15 15 32 63 
3 yrs. (%)        

Disclosures: No relevant conflicts of interest to declare.

Author notes

Corresponding author

Sign in via your Institution