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. 2023 Mar 23;28(8):737–e693. doi: 10.1093/oncolo/oyad019

Table 3.

Incidence of treatment-related adverse events attributed to cabozantinib.

Cabozantinib 20 mg plus avelumab (n = 3) Cabozantinib 40 mg plus avelumab (n = 3) Cabozantinib 60 mg plus avelumab (n = 6) Total (n = 12)
Adverse events, n (%) Any
grade
Grades
3-5
Any
grade
Grades
3-5
Any
grade
Grades
3-5
Any
grade
Grades
3-5
Diarrhea 3 (100) 1 (33.3) 1 (33.3) 6 (100) 1 (16.7) 10 (83.3) 2 (16.7)
Palmar-plantar erythrodysesthesia syndrome 1 (33.3) 2 (66.7) 5 (83.3) 1 (16.7) 8 (66.7) 1 (8.3)
Thromboembolic events 1
(33.3)
1
(33.3)
2 (66.7) 2 (66.7) 5 (83.3) 2 (33.3) 8 (58.3) 5 (25)
Dysgeusia 1 (33.3) 2 (66.7) 4 (66.7) 7 (58.3)
Mucositis oral 1 (33.3) 1 (33.3) 4 (66.7) 1 (16.7) 6 (50) 1 (8.3)
Anorexia 1 (33.3) 1 (33.3) 3 (50) 1 (16.7) 5 (41.7) 1 (8.3)
Fatigue 2 (66.7) 3 (50) 1 (16.7) 5 (41.7) 1 (8.3)
Hypokalemia 1 (33.3) 3 (50) 4 (33.3)
Hypothyroidism 1 (33.3) 1 (33.3) 3 (50) 5 (41.7)
Vomiting 3 (50) 3 (25)
ALT increased 2 (33.3) 1 (16.7) 2 (16.7) 1 (8.3)
AST increased 1 (33.3) 2 (33.3) 1 (16.7) 3 (25) 1 (8.3)
Hoarseness 2 (33.3) 2 (16.7)
Hypertension 1 (33.3) 1 (33.3) 2 (33.3) 2 (33.3) 3 (25) 3 (25)
Weight loss 1 (33.3) 1 (33.3) 2 (33.3) 4 (33.3)
Abdominal pain 1 (33.3) 1 (16.7) 2 (16.7)
Dry mouth 1 (33.3) 1 (16.7) 2 (16.7)
Dry skin 1 (33.3) 1 (16.7) 2 (16.7)
Epistaxis 1 (16.7) 1 (8.3)
Upset stomach 1 (16.7) 1 (8.3)
Cold Sores 1 (16.7) 1 (8.3)
Headache 1 (16.7) 1 (8.3)
Hyponatremia 1 (16.7) 1 (16.7) 1 (8.3) 1 (8.3)
Insomnia 1 (16.7) 1 (8.3)
Nail discoloration 1 (16.7) 1 (8.3)
Nausea 1 (33.3) 1 (16.7) 2 (16.7)
Oral dysesthesia 1 (33.3) 1 (16.7) 2 (16.7)
Pruritus 1 (16.7) 1 (8.3)
Rash maculo-papular 1 (33.3) 3 (100) 1 (33.3) 1 (16.7) 5 (41.7) 1 (8.3)
Skin irritation 1 (16.7) 1 (8.3)
Skin wound 1 (16.7) 1 (8.3)
Skin hyperpigmentation 1 (16.7) 1 (8.3)
Skin ulceration 1 (16.7) 1 (8.3)
Anemia 1 (33.3) 1 (33.3) 1 (8.3) 1 (8.3)
Arthralgia 1 (33.3) 1 (8.3)
Bruising 1 (33.3) 1 (8.3)
Cough 1 (33.3) 1 (8.3)
Dizziness 1 (33.3) 1 (8.3)
Gastroesophageal reflux disease 1 (33.3) 1 (8.3)
Muscle cramping 1 (33.3) 1 (8.3)
Hand-foot sensitivity 1 (33.3) 1 (8.3)
Face rash 1 (33.3) 1 (8.3)
Skin hypopigmentation 1 (33.3) 1 (8.3)
Stomach pain 1 (33.3) 1 (8.3)

€ = there were no grade 5 events in any patient.