Table 1 Most common pimasertib-related TEAEs (incidence 10% in any regimen; safety analysis set)

From: Clinical, pharmacokinetic and pharmacodynamic data for the MEK1/2 inhibitor pimasertib in patients with advanced hematologic malignancies

Treatment-related TEAEs

Regimen 1 (N=33)

Regimen 2 (N=32)

Regimen 3 (N=15)

Patients with at least one event, n (%)

25 (75.8)

21 (65.6)

14 (93.3)

 

Grade 1/2

Grade 3/4

Grade 1/2

Grade 3/4

Grade 1/2

Grade 3/4

Diarrhea

10 (30.3)

12 (34.4)

1 (3.1)

6 (40.0)

3 (20.0)

Nausea

7 (21.2)

2 (6.3)

2 (13.3)

1 (6.7)

Vomiting

4 (12.1)

1 (3.1)

2 (13.3)

1 (6.7)

Retinal detachment

2 (6.1)

5 (15.6)

1 (6.7)

Blurred vision

4 (12.1)

2 (6.3)

Peripheral edema

4 (12.1)

2 (6.3)

3 (20.0)

Fatigue

2 (6.1)

3 (9.4)

3 (20.0)

Face edema

1 (3.0)

1 (3.1)

3 (20.0)

Skin rash

3 (9.1)

4 (12.5)

4 (26.7)

Hypocalcemia

1 (3.1)

2 (13.3)

Hyperuricemia

2 (13.3)

AST increased

4 (12.1)

1 (3.1)

1 (6.7)

1 (6.7)

Blood ALP increased

2 (6.1)

1 (3.0)

1 (3.1)

2 (13.3)

  1. Abbreviations: ALP, alkaline phosphatase; AST, aspartate transaminase; TEAE, treatment-emergent adverse event.