Table 1

Baseline characteristics

Rituximab (n = 33)Placebo (n = 27)
Females, N (%) 19 (57.6) 16 (59.3) 
Age, median (IQR) 40 (30-59) 40 (31-59) 
ITP stage, N (%)   
    Newly diagnosed 17 (51.5) 11 (40.7) 
    Relapsed 16 (48.5) 16 (59.3) 
Duration of ITP, mo (median, IQR) 3 (1-47) 8 (1-40) 
Baseline platelet count, × 109/L (median, IQR) 15 (4-23) 14 (10-23) 
Standard treatments, N (%)   
    Prednisone 18 (54.5) 17 (63.0) 
    Dexamethasone 13 (39.4) 8 (29.6) 
    IVIg 13 (39.4) 9 (33.3) 
    Rhesus Ig 2 (6.1) 1 (3.7) 
    Solumedrol 2 (6.1) 
    Methylprednisolone 2 (6.1) 
    Romiplostim 1 (3.7) 
    Platelet transfusions 1 (3.0) 
    Combination 11 (33.3) 7 (25.9) 
Evaluation period, days* (median, IQR) 138 (130-144) 137 (114-142) 
Rituximab (n = 33)Placebo (n = 27)
Females, N (%) 19 (57.6) 16 (59.3) 
Age, median (IQR) 40 (30-59) 40 (31-59) 
ITP stage, N (%)   
    Newly diagnosed 17 (51.5) 11 (40.7) 
    Relapsed 16 (48.5) 16 (59.3) 
Duration of ITP, mo (median, IQR) 3 (1-47) 8 (1-40) 
Baseline platelet count, × 109/L (median, IQR) 15 (4-23) 14 (10-23) 
Standard treatments, N (%)   
    Prednisone 18 (54.5) 17 (63.0) 
    Dexamethasone 13 (39.4) 8 (29.6) 
    IVIg 13 (39.4) 9 (33.3) 
    Rhesus Ig 2 (6.1) 1 (3.7) 
    Solumedrol 2 (6.1) 
    Methylprednisolone 2 (6.1) 
    Romiplostim 1 (3.7) 
    Platelet transfusions 1 (3.0) 
    Combination 11 (33.3) 7 (25.9) 
Evaluation period, days* (median, IQR) 138 (130-144) 137 (114-142) 

IQR indicates interquartile range.

*

Evaluation period was from the completion of standard treatment (8 weeks from the start of standard treatment) until the end of follow-up (6 months from randomization).

Close Modal

or Create an Account

Close Modal
Close Modal