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Table 2 TEAEs in > 20% of patients receiving ripretiniba

From: Patient-reported outcomes in individuals with advanced gastrointestinal stromal tumor treated with ripretinib in the fourth-line setting: analysis from the phase 3 INVICTUS trial

Preferred term, n (%)

Ripretinib

(n = 85)

Placebo

(n = 43)

All grades

Grade 3–4

All grades

Grade 3–4

Alopecia

44 (52)

N/A

2 (4.7)

N/A

Fatigue

36 (42)

3 (3.5)

10 (23)

1 (2.3)

Nausea

33 (39)

3 (3.5)

5 (12)

0

Abdominal pain

31 (37)

6 (7.1)

13 (30)

2 (4.7)

Constipation

29 (34)

1 (1.2)

8 (19)

0

Myalgia

27 (32)

1 (1.2)

5 (12)

0

Diarrhea

24 (28)

1 (1.2)

6 (14)

1 (2.3)

Decreased appetite

23 (27)

1 (1.2)

9 (21)

1 (2.3)

PPESb

18 (21)

0

0

0

Vomiting

18 (21)

3 (3.5)

3 (7.0)

0

  1. N/A Not applicable, PPES Palmar-plantar erythrodysesthesia syndrome, TEAE Treatment-emergent adverse event
  2. aIncludes all TEAEs regardless of drug relatedness
  3. bThe highest severity classification for PPES is Grade 3