ately 4% of hairy cell leukemia patients, in each arm, died more than 60 days after the last dose of either treatment and there was no outstanding cause of death among these patients.
All Adverse
Events a
|
Percent of Patients |
Frontline, Treated With
NIPENT
N=180 |
Frontline, Treated With
IFN
N=176 |
IFN-Refractory Treated With
NIPENT
N=197 |
Nausea and/or
Vomiting
|
63 |
22 |
53 b |
Fever
|
46 |
59 |
42 |
Rash
|
43 |
30 |
26 |
Fatigue
|
42 |
55 |
29 |
Leukopenia
|
22 |
15 |
60 |
Pruritus
|
21 |
6 |
10 |
Coughing/Increased
Cough
|
20 |
15 |
17 |
Myalgia
|
19 |
36 |
11 |
Chills
|
19 |
34 |
11 |
Headache
|
17 |
29 |
13 |
Diarrhea
|
17 |
17 |
15 |
Abdominal Pain
|
16 |
15 |
4 |
Anorexia
|
13 |
10 |
16 |
Upper Respiratory
Infection
|
13 |
8 |
16 |
Asthenia
|
12 |
13 |
10 |
Stomatitis
|
12 |
7 |
5 |
Rhinitis
|
11 |
15 |
10 |
Dyspnea
|
11 |
13 |
8 |
Anemia
|
8 |
5 |
35 |
Pain
|
8 |
19 |
20 |
Pharyngitis
|
8 |
11 |
10 |
Sweating Increased/
Sweating
|
8 |
21 |
10 |
Viral Infection
|
8 |
17 |
NR |
Infection
|
7 c |
2 c |
36 |
Arthralgia
|
6 |
14 |
3 |
Thrombocytopenia
|
6 |
6 |
32 |
Skin Disorder
|
4 |
5 |
17 |
Allergic Reaction
|
2 |
1 |
11 |
Hepatic Disorder/
Elevated Liver
Function Tests d
|
2 |
2 |
|
|