Adverse event, (≥10%) | All treatment (n = 30) | Post‐reduction (n = 26) | ||
---|---|---|---|---|
All grade, n (%) | Grade 3–4, n (%) | All grade, n (%) | Grade 3–4, n (%) | |
Any cause | 30 (100) | 14 (47) | 24 (92) | 4 (15) |
Diarrhea | 29 (97) | 3 (10) | 7 (27) | 0 (0) |
Rash/acne | 22 (73) | 2 (4) | 14 (54) | 1 (4) |
Paronychia | 18 (60) | 4 (13) | 15 (58) | 1 (4) |
Stomatitis | 18 (60) | 2 (7) | 5 (19) | 0 (0) |
Elevation of AST/ALT | 11 (37) | 3 (10) | 6 (24) | 2 (8) |
Anorexia | 8 (27) | 2 (7) | 0 (0) | 0 (0) |
Pruritus | 6 (20) | 0 (0) | 2 (8) | 0 (0) |
Dry skin | 4 (13) | 1 (3) | 3 (12) | 0 (0) |
Anemia | 5 (17) | 0 (0) | 3 (12) | 0 (0) |
Interstitial lung disease | 3 (10) | 1 (3) | 2 (8) | 0 (0) |
Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase. | ||||
Adverse Events Legend | ||||
The rate of all‐cause AEs grade ≥ 3 was 57% (17 of 30). Interstitial lung disease occurred in three patients, and one patient died. Two treatment‐related deaths from interstitial lung disease, and acute cardiac failure were observed. |