Table 3.
Any Grade Adverse Events That Occurred in ≥2 Patients | N (%) |
---|---|
Fatigue | 4 (66.7) |
Pruritis | 2 (33.3) |
Rash | 3 (50) |
Decreased appetite | 2 (33.3) |
Headaches | 2 (33.3) |
Neuropathy | 2 (33.3) |
Dyspnea (pneumonitis ruled out) | 2 (33.3) |
Nausea | 4 (66.7) |
Diarrhea (colitis ruled out) | 3 (50) |
Rectal bleeding | 2 (33.3) |
Dehydration | 2 (33.3) |
Grade ≥3 adverse events that occurred in ≥1 patient | N, (%) |
Hepatitis (grade 3) | 1 (16.7) |
Nausea (grade 3) | 1 (16.7) |
Mouth sores (grade 3) | 1 (16.7) |
Diarrhea (colitis ruled out) (grade 3) | 1 (16.7) |
Adverse events of special interest | |
Focal pneumonitis (grade 2) | 1 (16.7) |