Table 6.

Incidence of WHO grade-3 to grade-4 side effects during induction therapy




Group A, G-CSF-/-

Group B, G-CSF+/-

Group C, G-CSF-/+

Group D, G-CSF+/+
N   178   172   173   177  
Hemorrhage   9 (5.0)   15 (8.8)   13 (7.5)   7 (4.0)  
Hepatic   14 (7.9)   13 (7.5)   21 (12.1)   22 (12.4)  
Cardiovascular*  23 (12.9)   11 (6.4)   15 (8.7)   20 (11.3)  
Hypotension   2 (1.1)   2 (1.2)   8 (4.6)   7 (4.0)  
Diarrhea   10 (5.6)   3 (1.8)   8 (4.6)   7 (4.0)  
Nausea   38 (21.4)   40 (23.3)   30 (17.4)   28 (15.8)  
Rigors/chills   0 (0)   0 (0)   2 (1.2)   1 (0.6)  
Bone pain   1 (0.6)   0 (0)   1 (0.6)   2 (1.1)  
Rash/itch   2 (1.1)   4 (2.3)   6 (3.5)   7 (4.0)  
Infection
 
48 (27.0)
 
57 (23.1)
 
54 (31.2)
 
45 (25.4)
 



Group A, G-CSF-/-

Group B, G-CSF+/-

Group C, G-CSF-/+

Group D, G-CSF+/+
N   178   172   173   177  
Hemorrhage   9 (5.0)   15 (8.8)   13 (7.5)   7 (4.0)  
Hepatic   14 (7.9)   13 (7.5)   21 (12.1)   22 (12.4)  
Cardiovascular*  23 (12.9)   11 (6.4)   15 (8.7)   20 (11.3)  
Hypotension   2 (1.1)   2 (1.2)   8 (4.6)   7 (4.0)  
Diarrhea   10 (5.6)   3 (1.8)   8 (4.6)   7 (4.0)  
Nausea   38 (21.4)   40 (23.3)   30 (17.4)   28 (15.8)  
Rigors/chills   0 (0)   0 (0)   2 (1.2)   1 (0.6)  
Bone pain   1 (0.6)   0 (0)   1 (0.6)   2 (1.1)  
Rash/itch   2 (1.1)   4 (2.3)   6 (3.5)   7 (4.0)  
Infection
 
48 (27.0)
 
57 (23.1)
 
54 (31.2)
 
45 (25.4)
 

Results are presented as absolute numbers, with the percentages in parentheses.

-/-, indicates not administered on days 1 to 7; +/-, administered on days 1 to 7; -/+, not administered on days 8 to 28; and +/+, administered on days 8 to 28.

*

Includes nonspecific cardiac events and dysrhythmias.

or Create an Account

Close Modal
Close Modal