Table 4.

Treatment Related Adverse Events.

Adverse Events	Any Grade, n (%)	Grade 3/4, n (%)
Rash	4(25.0%)	1(6.3%)
Diarrhea	4(25.0%)	0
Aspartate aminotransferase increase	3(18.8%)	1(6.3%)
Alanine transaminase increase	3(18.8%)	1(6.3%)
Decreased appetite	3(18.8%)	0
Fatigue	3(18.8%)	0
Pruritus	2(12.5%)	0
Dental ulcer	2(12.5%)	0
Nausea	2(12.5%)	0
Hypertension	1(6.3%)	0
Infusion-related reaction	1(6.3%)	0
Gastrointestinal hemorrhage	1(6.3%)	1(6.3%)
Blood bilirubin increase	1(6.3%)	0
Weight decrease	1(6.3%)	0