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. 2016 Jul 4;10:59–66. doi: 10.4137/CMO.S38335

Table 3.

Treatment-related adverse events.

TOXICITY TYPE ANY GRADE (G) GRADE ≤2 GRADE 3 GRADE 4
Any event n(%) 25 (86) 13 (45) 7 (24) 3* (10)
Clinical adverse events
Fatigue 10 (35) 9 (31) 1 (3,5)
Diarrhea 6 (20) 6 (20)
Hand foot syndrome 6 (20) 4 (14) 2 (7)
Rash 5 (17) 3 (10) 1 (3,5) 1*(3,5)
Anorexia 4 (14) 4 (14)
Oral mucositis 4 (14) 4 (14)
Muscle pain 3 (10) 3 (10)
Abdominal pain 3 (10) 3 (10)
Voice changes 3 (10) 3 (10)
Bleed 2 (7,0) 1 (3,5) 1*(3,5)
Nausea/Vomiting 1 (3,5) 1 (3,5)
Hypertension 1 (3,5) 1 (3,5)
Heart failure 1 (3,5) 1*(3,5)
Laboratory abnormalities
Thrombocytopenia 5 (17) 3 (10) 2 (7,0)
Neutropenia 3 (10) 2 (7,0) 1 (3,5)
Anemia 1 (3,5) 1 (3,5)

Note:

*

Hospitalization due to severe adverse events.