Main characteristics of the landmark cohort (n = 807) at inclusion and landmark
Variable . | Inclusion visit (n = 807) . | 6-mo landmark visit . | ||
---|---|---|---|---|
n or median . | % or IQR . | n 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 | 1 | 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 | 5 | 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 | 2 | 0.3% | 4 | 0.5% |
HMA | 1 | 0.1% | 16 | 2.0% |
HY | 0 | 0% | 3 | 0.4% |
LEN | 3 | 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 |
Variable . | Inclusion visit (n = 807) . | 6-mo landmark visit . | ||
---|---|---|---|---|
n or median . | % or IQR . | n 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 | 1 | 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 | 5 | 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 | 2 | 0.3% | 4 | 0.5% |
HMA | 1 | 0.1% | 16 | 2.0% |
HY | 0 | 0% | 3 | 0.4% |
LEN | 3 | 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.