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. 2016 May 12;114(11):1185–1190. doi: 10.1038/bjc.2016.125

Table 3. Adverse events.

NCI-CTCAE v4.03 Any grade Grades 1–2 Grades 3–4
Anaemia 41 (91%) 31 (69%) 10 (22%)
Neutropenia 36 (80%) 18 (40%) 18 (40%)
Thrombocytopenia 29 (64%) 24 (53%) 5 (11%)
Febrile neutropenia 1 (2%) 0 1 (2%)
Alopecia 12 (27%) 12 (27%) 0
Anorexia 42 (93%) 28 (62%) 14 (31%)
Nausea 33 (73%) 30 (67%) 3 (7%)
Vomiting 17 (38%) 13 (29%) 4 (9%)
Constipation 17 (38%) 17 (38%) 0
Diarrhoea 17 (38%) 16 (36%) 1 (2%)
Abdominal pain 18 (40%) 15 (33%) 3 (7%)
Fatigue 42 (93%) 27 (60%) 15 (33%)
Hand-foot skin reaction 19 (42%) 18 (40%) 1 (2%)
Hyperpigmentation 18 (40%) 18 (40%) 0
Nail change 10 (22%) 10 (22%) 0
Neuropathy–sensory 14 (31%) 13 (29%) 1 (2%)
Stomatitis 26 (58%) 20 (44%) 6 (13%)
Dysgeusia 14 (31%) 14 (31%) 0
Thrombosis/embolism 12 (27%) 0 12 (27%)
Arterial 5 (11%) 0 5 (11%)
Venous 7 (16%) 0 7 (16%)

Abbreviation: NCI-CTCAE v4.03=National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03.