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. 2021 Mar 10;3(4):234–240. doi: 10.1253/circrep.CR-21-0008

Table 2.

Adverse Events After Initiation of Axitinib

  All patients (n=22) TKI(−) (n=11) TKI(+) (n=11)
All grades ≥Grade 3 All grades ≥Grade 3 All grades ≥Grade 3
Hypertension 18 (81.8) 8 (36.4) 9 (81.8) 4 (36.4) 9 (81.8) 4 (36.4)
Diarrhea 17 (77.3) 4 (18.2) 10 (90.9) 3 (27.3) 7 (63.6) 1 (9.1)
Hypothyroidism 12 (54.5) 4 (18.2) 7 (63.6) 3 (27.3) 5 (45.4) 1 (9.1)
Proteinuria 10 (45.5) 4 (18.2) 6 (54.5) 3 (27.3) 4 (36.4) 1 (9.1)
Hand–foot syndrome 8 (36.4) A 5 (45.4) A 3 (27.3) A
Hoarseness 6 (27.3) 0 4 (36.4) 0 2 (18.2) 0
Appetite loss 6 (27.3) 0 4 (36.4) 0 2 (18.2) 0
Fatigue 4 (18.2) 0 2 (18.2) 0 2 (18.2) 0
Fever 2 (9.1) 1 (4.5) 1 (9.1) 1 (9.1) 1 (9.1) 0
Vomiting 2 (9.1) 0 1 (9.1) 0 1 (9.1) 0
Sinusitis 1 (9.1) 0 0 0 1 (9.1) 0
Stomatitis 1 (9.1) 0 0 0 1 (9.1) 0
Otitis externa 1 (4.5) 1 (4.5) 1 (9.1) 1 (9.1) 0 0
Cerebral infarct 1 (4.5) 1 (4.5) 1 (9.1) 1 (9.1) 0 0

Data are presented as n (%). AThere was no classification of ≥Grade 3 for hand–foot syndrome according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. TKI, tyrosine kinase inhibitor.