Table 3 –

Adverse event data

Adverse event a	Acute b	Late c	Overall
Nausea	3	0	3
Vomiting	2	0	2
Creatinine increase	0	2	2
Urinary frequency	1	0	1
Thrombocytopenia	0	1	1
Hematuria	1	0	1
Fatigue	0	1	1
Total	7	4	11

^aAll events were grade 1.

^bPresent in the first 3 mo of follow-up.

^cPresent at longer than 3-mo follow-up.