Table 1

Baseline characteristics for patients enrolled on lenalidomide monotherapy and lenalidomide and (rhu-EPO) combined therapy

Monotherapy (n = 39)Combination therapy (n = 23)
Mean age, y 70.8 70.1 
Sex 
    Male 28 (71.8%) 18 (78.3%) 
    Female 11 (28.2%) 5 (21.7%) 
ECOG performance status 
    0 7 (17.9%) 6 (26.1%) 
    1 31 (79.5) 17 (73.9%) 
    2 1 (2.6%) 
Median duration of MDS, y (range) 1.9 (0.4-13.3) 3.2 
Median RBC transfusion burden for 4 weeks, n (range) 4 (2.0-10.0)  
MDS FAB subtype, n (%) 
    RA 11 (28%) 7 (30%) 
    RARS 15 (38.5%) 7 (30%) 
    RCMD 4 (10.0%) 3 (13%) 
    RAEB 8 (21%) 5 (22%) 
    CMML 1 (2.5%) 1 (4.3%) 
Cytogenetics, n (%) 
    Non-del(5q) 32 (82%) 19 (83%) 
    del(5q) 7 (18%) 4 (17%) 
IPSS, n (%) 
    Low risk 18 (46.2%) 11 (47.8%) 
    Intermediate-1 risk 21 (53.8%) 12 (52.2%) 
Serum EPO level 
    Mean, IU (SD) 955 (1652) 600 (921) 
    Patients > 500 IU, n (%) 15/36 (39%) 7/23 (30%) 
Monotherapy (n = 39)Combination therapy (n = 23)
Mean age, y 70.8 70.1 
Sex 
    Male 28 (71.8%) 18 (78.3%) 
    Female 11 (28.2%) 5 (21.7%) 
ECOG performance status 
    0 7 (17.9%) 6 (26.1%) 
    1 31 (79.5) 17 (73.9%) 
    2 1 (2.6%) 
Median duration of MDS, y (range) 1.9 (0.4-13.3) 3.2 
Median RBC transfusion burden for 4 weeks, n (range) 4 (2.0-10.0)  
MDS FAB subtype, n (%) 
    RA 11 (28%) 7 (30%) 
    RARS 15 (38.5%) 7 (30%) 
    RCMD 4 (10.0%) 3 (13%) 
    RAEB 8 (21%) 5 (22%) 
    CMML 1 (2.5%) 1 (4.3%) 
Cytogenetics, n (%) 
    Non-del(5q) 32 (82%) 19 (83%) 
    del(5q) 7 (18%) 4 (17%) 
IPSS, n (%) 
    Low risk 18 (46.2%) 11 (47.8%) 
    Intermediate-1 risk 21 (53.8%) 12 (52.2%) 
Serum EPO level 
    Mean, IU (SD) 955 (1652) 600 (921) 
    Patients > 500 IU, n (%) 15/36 (39%) 7/23 (30%) 

CMML indicates chronic myelomonocytic leukemia; FAB, French-American-British system; RA, refractory anemia; RAEB, refractory anemia with excess blasts; RARS, refractory anemia with ring sideroblasts; and CMD, refractory cytopenia with multilineage dysplasia.

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