Skip to main content

Table 3 Treatment-emergent serious adverse events (safety population)

From: Safety and tolerability of quizartinib, a FLT3 inhibitor, in advanced solid tumors: a phase 1 dose-escalation trial

Serious adverse events (SAEs)

Treatment group, 90 mg (n = 8)

Treatment group, 135 mg (n = 5)

Total (N = 13)

Patients with any SAE n (%)

2 (25.0)

2 (40.0)

4 (30.8)

 Anemia

1 (12.5)

0

1 (7.7)

 Febrile neutropenia

0

1 (20.0)

1 (7.7)

 Leukopenia

1 (12.5)

0

1 (7.7)

 Pancytopenia

0

1 (20.0)

1 (7.7)

 Thrombocytopenia

1 (12.5)

0

1 (7.7)

 Pneumonia

1 (12.5)

0

1 (7.7)

 Urosepsis

0

1 (20.0)

1 (7.7)

 Peritoneal hemorrhage

1 (12.5)

0

1 (7.7)

  1. The same patient may have experienced more than 1 SAE