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. 2016 May 12;16:306. doi: 10.1186/s12885-016-2338-6

Table 3.

Adverse events (All cycles)

N = 12 CTC-AE grade (Ver. 4.03)
1 2 3 4 3/4 (%)
Leukopenia 1 3 3 0 3 (25 %)
Neutropenia 2 3 3 0 3 (25 %)
Anemia 4 1 1 0 1 (8 %)
Thrombocytopenia 4 0 1 0 1 (8 %)
Febrile Neutropenia 0 0 1 0 1 (8 %)
Hypoalbuminemia 7 1 0 0 0 (0 %)
T-Bil elevation 1 1 0 0 0 (0 %)
AST elevation 6 0 0 0 0 (0 %)
ALT elevation 4 0 0 0 0 (0 %)
ALP elevation 4 0 0 0 0 (0 %)
Cre elevation 3 0 0 0 0 (0 %)
Hyperkalemia 2 0 0 0 0 (0 %)
Hypercalcemia 2 0 0 0 0 (0 %)
Hyponatremia 2 0 0 0 0 (0 %)
Fatigue 3 1 1 0 1 (8 %)
Anorexia 4 3 1 0 1 (8 %)
Weight loss 1 1 0 0 0 (0 %)
Nausea 1 2 1 0 1 (8 %)
Vomiting 2 0 0 0 0 (0 %)
Constipation 2 4 0 0 0 (0 %)
Perforation (colon) 0 0 1 0 1 (8 %)
Hypertension 1 2 0 0 0 (0 %)
Epistaxis 3 0 0 0 0 (0 %)
Stroke 0 1 0 0 0 (0 %)
Urticaria 1 1 0 0 0 (0 %)
Pruritus 2 0 0 0 0 (0 %)
Pneumonitis 2 0 0 0 0 (0 %)

CTC-AE common terminology criteria for adverse events