Skip to main content
. 2023 Apr 27;28(7):618–623. doi: 10.1093/oncolo/oyad085

Table 3.

Treatment-related adverse events.

Adverse event Maximum grade
1 2 3 4 Total
Abdominal pain 3 0 0 0 3
Alanine aminotransferase—increased 4 0 1 0 5
Alkaline phosphatase—increased 2 0 1 0 3
Anorexia 1 0 0 0 1
Anxiety 1 1 0 0 2
Arthralgia 1 0 0 0 1
Arthritis 0 0 1 0 1
Ascites 0 0 1 0 1
Aspartate aminotransferase—increased 3 0 1 0 4
Blood bilirubin increased 2 0 0 0 2
CPK increased 2 0 0 0 2
Cholecystitis 0 0 1 0 1
Cough 1 0 0 0 1
Creatinine increased 0 1 0 0 1
Dizziness 1 0 0 0 1
Dry mouth 0 1 0 0 1
Dyspnea 0 1 0 0 1
Eosinophilia 1 0 0 0 1
Fatigue 7 3 0 0 10
Fever 1 0 0 0 1
Headache 1 0 0 0 1
Hyperglycemia 1 0 0 0 1
Hyperthyroidism 1 1 0 0 2
Hypokalemia 1 1 1 0 3
Hyponatremia 1 0 1 0 2
Hypothyroidism 0 4 0 0 4
Injection site reaction 0 21 0 0 21
Lipase increased 2 1 0 1 4
Lymphopenia 3 0 0 0 3
Mucositis oral 0 1 0 0 1
Nausea 3 1 0 0 4
Neutropenia 0 0 1 0 1
Pain 0 1 0 0 1
Pain in extremity 1 4 0 0 5
Thrombocytopenia 2 0 0 0 2
Rash maculo-papular 3 0 0 0 3
Serum amylase increased 2 0 1 0 3
Sinus bradycardia 1 0 0 0 1
Vomiting 1 0 0 0 1