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. 2020 Mar 6;10:202. doi: 10.3389/fonc.2020.00202

Table 2.

Treatment-related adverse events.

Event Gradea 1 Grade 2 Grade 3 Grade 4/5
n (%)
Fever 22 (65) 1 (3) 0 0
Nausea 9 (26) 1 (3) 0 0
Musculoskeletal pain 8 (24) 1 (3) 1 (3) 0
Vomiting 6 (18) 0 0 0
Asthenia 5 (15) 3 (9) 1 (3) 0
Headache 3 (9) 0 0 0
Injection site reaction/erythema 2 (6) 0 0 0
Bradycardia 1 (3) 0 0 0
Diarrhea 1 (3) 1 (3) 0 0
Nail dyschromia 1 (3) 0 0 0
Local pain 1 (3) 0 0 0
Epigastric pain 1 (3) 1 (3) 0 0
Injection site reaction/swelling 1 (3) 0 0 0
Herpes labialis 1 (3) 0 0 0
Injection site reaction/hyperemia 1 (3) 0 0 0
Hypotension 1 (3) 0 0 0
Mild visus decrease 1 (3) 0 0 0
Loss of appetite 1 (3) 0 0 0
Agitation 1 (3) 0 0 0
Vertigo 1 (3) 0 0 0
Anemia 0 1 (3) 0 0
Abdominal pain 0 1 (3) 0 0
Neutropenia 0 1 (3) 0 0
Persistent coughing 0 1 (3) 0 0
a

Grades of adverse events were defined according to the National Cancer Institute CTCAE, version 4.0.