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. 2021 Apr 20;10(5):473–484. doi: 10.1159/000515552

Table 7.

Adverse events (>10%) during treatment with regorafenib after lenvatinib in patients with advanced HCC

Events Regorafenib (any lines) (n = 22) Regorafenib (third line) (n = 17)
any (%) grade ≥3 (%) any (%) grade ≥3 (%)
Aspartate aminotransferase increased 13 (59.1) 2 (9.1) 11 (64.7) 2 (11.8)
Proteinuria 12 (54.6) 0 9 (52.9) 0
Hypertension 10 (45.6) 2 (9.1) 9 (52.9) 2 (11.8)
Fatigue 9 (40.9) 0 7 (41.2) 0
Palmar-plantar erythrodysesthesia 8 (36.4) 2 (9.1) 4 (23.5) 0
Hypoalbuminemia 8 (36.4) 0 8 (47.1) 0
Anorexia 7 (31.8) 0 6 (35.3) 0
Bilirubin increased 7 (31.8) 3 (13.6) 7 (41.2) 3 (17.6)
Diarrhea 6 (27.3) 1 (4.5) 4 (23.5) 1 (5.9)
Hypothyroidism 5 (22.7) 0 4 (23.5) 0
Anemia 5 (22.7) 0 5 (29.4) 0
Thrombocytopenia 5 (22.7) 2 (9.1) 5 (29.4) 2 (11.8)
Serum amylase increased 4 (18.2) 0 3 (17.6) 0
Weight loss 3 (13.6) 0 3 (17.6) 0

HCC, hepatocellular carcinoma.