Table 3. Adverse events reported in patients (n=30) during CE (115 cycles).

	NCI-CTC grade 3 or 4
Adverse event	No. of patients	%
Thrombocytopenia	0	0
Neutropenia	6	20
Nausea	0	0
Vomiting	0	0
Constipation	0	0
Ototoxicity	1	3.3