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. 2021 Jun 10;19:168. doi: 10.1186/s12957-021-02280-9

Table 4.

Adverse events occurring during adjuvant sorafenib therapy in seven comparative studies

Author Sample size Fatigue, N (%) Hand-foot skin reaction, N (%) Alopecia, N (%) Rash or desquamation, N (%) Hypertension, N (%) Anorexia, N (%) Hematological events, N (%) Transaminase elevation, N (%) Diarrhea, N (%)
All grades Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4 All grade Grade 3 or 4
Bruix J 556 73 (13) 9 (1) 389 (70) 154 (28) 179 (32) 91 (16) 4 (3) 108 (19) 24 (4) 33 (6) 2 (< 1) 32 (6) 9 (1) 100 (18) 56 (10) 215 (38) 34 (6)
Li J 12 NA NA 11 (92) NA NA NA NA NA NA 10 (83) NA NA NA NA NA NA 10 (83.3) NA
Chen BF 24 12 (50) NA 10 (42) NA 9 (38) NA 7 (29) NA 5 (21) NA 14 (58) NA 5 (21) NA NA NA 7 (29) NA
Zhuang L 27 3 (11.1) 0 (0) 16 (59.2) 2 (7.4) 3 (11.1) 0 (0) 5 (18.5) 0 (0) 1 (3.7) 0 (0) 3 (11.1) 0 (0) NA NA NA NA 5 (18.5) 1 (3.7)
Wang DS 98 NA NA 3 (2.8) NA NA NA NA NA NA NA NA NA 21 (21.4) NA 20 (20.4) NA 7 (6.5) NA
Zhang W 32 Grade 3 adverse effects occurred in 6 patients with sorafenib treatment (18.8%)
Xia F 34 With only grades 1 and 2 drug-related adverse events (14 patients, 41.2% in this study)

NA not available