Table 5.

Adverse events that have been reported in at least 20% of the patients in at least one of the treatment arms



DNR/Ara-C; N = 211

DNR/Ara-C + PSC-833; N = 202*
AE
CTC 1-2, %
CTC 3-4, %
CTC 1-2, %
CTC 3-4, %
Abdominal pain   21   1   31   3  
Anorexia   16   4   17   3  
Constipation   26   1   34   1  
Coughing   23   1   25   2  
Diarrhea   43   8   58   6  
Dizziness   11   1   25   2  
Dyspnea   18   10   22   11  
Epistaxis   21   1   20   1  
Febrile neutropenia/fever   51   38   51   33  
Fluid overload   18   3   21   2  
Headache   25   1   24   2  
Herpes simplex   20   1   22   3  
Hypertension   5   8   17   8  
Hypokalemia   31   4   35   4  
Hypotension   9   6   16   9  
Infection   11   14   11   13  
Injection site reaction   28   4   25   6  
Mucositis n.o.s.   18   4   20   8  
Nausea   49   5   47   9  
Purpura   17   2   22   0  
Rash   30   2   29   6  
Rash erythematous   24   1   27   4  
Rigors   27   1   27   2  
Sepsis   12   24   20   19  
Thrombocytopenia   4   19   3   17  
Vomiting
 
43
 
0
 
48
 
2
 


DNR/Ara-C; N = 211

DNR/Ara-C + PSC-833; N = 202*
AE
CTC 1-2, %
CTC 3-4, %
CTC 1-2, %
CTC 3-4, %
Abdominal pain   21   1   31   3  
Anorexia   16   4   17   3  
Constipation   26   1   34   1  
Coughing   23   1   25   2  
Diarrhea   43   8   58   6  
Dizziness   11   1   25   2  
Dyspnea   18   10   22   11  
Epistaxis   21   1   20   1  
Febrile neutropenia/fever   51   38   51   33  
Fluid overload   18   3   21   2  
Headache   25   1   24   2  
Herpes simplex   20   1   22   3  
Hypertension   5   8   17   8  
Hypokalemia   31   4   35   4  
Hypotension   9   6   16   9  
Infection   11   14   11   13  
Injection site reaction   28   4   25   6  
Mucositis n.o.s.   18   4   20   8  
Nausea   49   5   47   9  
Purpura   17   2   22   0  
Rash   30   2   29   6  
Rash erythematous   24   1   27   4  
Rigors   27   1   27   2  
Sepsis   12   24   20   19  
Thrombocytopenia   4   19   3   17  
Vomiting
 
43
 
0
 
48
 
2
 

Per treatment arm and per AE, the proportion of patients with a maximum grade 1-2 or 3-4 are shown. Proportions are rounded to the nearest integer. AEs were graded according to the NCIC Expanded CTC.

n.o.s. indicates not otherwise specified.

*

The 6 patients in the PSC-833 arm who did not receive any protocol treatment have been excluded.

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