Table 6.

Common Terminology Criteria for Adverse Events (CTCAE) reporting gastrointestinal toxicity scores at time-points after salvage high- dose-rate brachytherapy (sHDR-BT)

Parameter		1 month post-sHDR-BT	3 months post-sHDR-BT
Anal pain, n (%)
	0	16 (94)	16 (94)
	1	1 (6)	0 (0)
	2	0 (0)	1 (6)
Diarrhea, n (%)
	0	16 (94)	17 (100)
	1	1 (6)	0 (0)
Flatulence, n (%)
	0	16 (94)	16 (94)
	1	1 (6)	1 (6)
Nausea, n (%)
	0	16 (94)	17 (100)
	1	1 (6)	0 (0)
Proctitis, n (%)
	0	17 (100)	16 (94)
	1	0 (0)	1 (6)
Rectal mucositis, n (%)
	0	15 (88)	16 (94)
	1	2 (12)	1 (6)
Rectal pain, n (%)
	0	17 (100)	16 (94)
	1	0 (0)	1 (6)