Table 5. Summary of adverse events experienced by at least 10% of 52 patients treated with lapatinib plus capecitabine.
Adverse event | Grade 1 | Grade 2 | Grade 3 | Grade 4 | Total |
PPE | 25 (48.1) | 6 (11.5) | 0 | 0 | 31 (59.6) |
Diarrhea | 20 (38.5) | 4 (7.7) | 0 | 0 | 25 (48.1)a |
Rash | 22 (42.3) | 1 (1.9) | 2 (3.8) | 0 | 25 (48.1) |
Hyperbilirubinemia | 4 (7.7) | 12 (23.1) | 2 (3.8) | 0 | 18 (34.6) |
Fatigue | 11 (21.2) | 4 (7.7) | 1 (1.9) | 0 | 16 (30.8) |
Nausea | 9 (17.3) | 1 (1.9) | 0 | 0 | 10 (19.2) |
Neutropenia | 0 | 4 (7.7) | 1 (1.9) | 2 (3.8) | 7 (13.5) |
Data are presented as number of patients, with the percentage in parentheses.
aThe grade of diarrhea for one patient (1.9%) was unknown.
PPE, palmar-plantar erythrodysesthesia.