Table 1.

Main characteristics of the landmark cohort (n = 807) at inclusion and landmark

VariableInclusion visit (n = 807)6-mo landmark visit
n or median% or IQRn or median% or IQR
Sex     
 Male 497 61.6%   
 Female 310 38.4%   
Age, y 73 67-79   
WHO classification at diagnosis     
 RA 141 17.5%   
 RARS 139 17.2%   
 RCMD 309 38.3%   
 RCMD-RS 51 6.3%   
 5q− syndrome 49 6.1%   
 RAEB-1 94 11.7%   
 RAEB-2 0.1%   
 MDS-U 23 2.9%   
IPSS-R cytogenetic risk (n = 730)     
 Very good 84 11.5%   
 Good 543 74.4%   
 Intermediate 89 12.1%   
 Poor/very poor 14 2.00%   
IPSS-R risk (available in 691 patients*)     
 Very low 180 26.0%   
 Low 297 43.0%   
 Intermediate 167 24.2%   
 High 42 6.1%   
 Very high 0.7%   
Hb level, g/dL 10.1 9-11.3   
RBC-TD     
 No 601 74.5% 592 73.4% 
 Yes 206 25.5% 215 26.6% 
Platelets, ×109/L 181 102-277 169 93-263 
Neutrophils, ×109/L 2.4 1.4-3.9 2.3 1.4-3.7 
Treatment before visit     
 ESA with or without G-CSF 115 14.2% 277 34.3% 
 G-CSF alone 0.3% 0.5% 
 HMA 0.1% 16 2.0% 
 HY 0% 0.4% 
 LEN 0.4% 22 2.7% 
 None 686 85% 485 60.1% 
Time from diagnosis to inclusion, d 37 19-61   
Time from inclusion to landmark, mo   6.1 5.7-6.4 
Follow-up from landmark, mo   37.8 17.0-58.8 
VariableInclusion visit (n = 807)6-mo landmark visit
n or median% or IQRn or median% or IQR
Sex     
 Male 497 61.6%   
 Female 310 38.4%   
Age, y 73 67-79   
WHO classification at diagnosis     
 RA 141 17.5%   
 RARS 139 17.2%   
 RCMD 309 38.3%   
 RCMD-RS 51 6.3%   
 5q− syndrome 49 6.1%   
 RAEB-1 94 11.7%   
 RAEB-2 0.1%   
 MDS-U 23 2.9%   
IPSS-R cytogenetic risk (n = 730)     
 Very good 84 11.5%   
 Good 543 74.4%   
 Intermediate 89 12.1%   
 Poor/very poor 14 2.00%   
IPSS-R risk (available in 691 patients*)     
 Very low 180 26.0%   
 Low 297 43.0%   
 Intermediate 167 24.2%   
 High 42 6.1%   
 Very high 0.7%   
Hb level, g/dL 10.1 9-11.3   
RBC-TD     
 No 601 74.5% 592 73.4% 
 Yes 206 25.5% 215 26.6% 
Platelets, ×109/L 181 102-277 169 93-263 
Neutrophils, ×109/L 2.4 1.4-3.9 2.3 1.4-3.7 
Treatment before visit     
 ESA with or without G-CSF 115 14.2% 277 34.3% 
 G-CSF alone 0.3% 0.5% 
 HMA 0.1% 16 2.0% 
 HY 0% 0.4% 
 LEN 0.4% 22 2.7% 
 None 686 85% 485 60.1% 
Time from diagnosis to inclusion, d 37 19-61   
Time from inclusion to landmark, mo   6.1 5.7-6.4 
Follow-up from landmark, mo   37.8 17.0-58.8 

G-CSF, granulocyte colony-stimulating factor; MDS-U, MDS unclassified; RA, refractory anemia; RAEB, refractory anemia with excess of blasts; RARS, refractory anemia with ringed sideroblasts; RCMD, refractory cytopenia with multilineage dysplasia; RCMD-RD, refractory cytopenia with multilineage dysplasia and ringed sideroblasts.

*

Detailed cytogenetics missing in 77 patients; detailed BM blasts (total <5%) missing in 39 patients.

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