Table 2.

Treatment-Related Toxicity

	All treated patients (N=12)
	Grade 1	Grade 2	Total
Any treatment-related adverse event	5 (42%)	3 (25%)	8 (67%)
Diarrhea	5 (42%)	1 (8%)	6 (50%)
Fatigue	1 (8%)	1 (8%)	2 (17%)
Dermatitis acneiform	2 (17%)	-	2 (17%)
Mucosal inflammation	1 (8%)	-	1 (8%)
Folliculitis	1 (8%)	-	1 (8%)
Tinea cruris	1 (8%)	-	1 (8%)
Myalgia	1 (8%)	-	1 (8%)
Dysgeusia	-	1 (8%)	1 (8%)
Headache	1 (8%)	-	1 (8%)
Oropharyngeal pain	1 (8%)	-	1 (8%)
Sinus Congestion	1 (8%)	-	1 (8%)
Flushing	1 (8%)	-	1 (8%)

All treatment-related toxicity was ≤ grade 2. Data are shown as n (%).