Table 3. Adverse events (maximum grade attributable to drug).

Adverse event (n=36)	Grade 1, 2, n [%]	Grade 3, 4, n [%]	Overall, n [%]
Fatigue	19 [53]	7 [19]	26 [72]
Nausea	19 [53]	6 [17]	25 [69]
Neuropathy-sensory	21 [58]	1 [3]	22 [61]
Vomiting	15 [42]	4 [1]	19 [53]
Anorexia	15 [42]	1 [3]	16 [44]
Anemia	11 [31]	3 [8]	14 [39]
Diarrhea	8 [22]	5 [14]	13 [36]
Hand-foot skin reaction	8 [22]	1 [3]	9 [25]
Abdominal pain or cramping	4 [11]	3 [8]	7 [19]
Thrombocytopenia	7 [19]	0 [0]	7 [19]

Note: one patient who received treatment was missing safety data.