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Table 3 Treatment-related adverse effects of all grades

From: Hepatic artery infusion of FOLFOX chemotherapy plus camrelizumab combined with sorafenib for advanced hepatocellular carcinoma in Barcelona Clinic Liver Cancer stage C (Double-IA-001): a phase II trial

Categories

Any grade

Grades 1 and 2

Grade 3 or higher

Aspartate aminotransferase increased

25 (100.0%)

14 (56.0%)

11 (44.0%)

Alanine aminotransferase increased

22 (88.0%)

15 (60.0%)

7 (28.0%)

Hypoalbuminemia

22 (88.0%)

22 (88.0%)

0 (0.0%)

Neutrophil count decreased

11 (44.0%)

9 (36.0%)

2 (8.0%)

Lymphocyte count decreased

24 (96.0%)

11 (44.0%)

13 (52.0%)

Anemia

20 (80.0%)

17 (68.0%)

3 (12.0%)

Platelet count decreased

15 (60.0%)

10 (40.0%)

5 (20.0%)

Blood bilirubin increased

18 (72.0%)

13 (52.0%)

5 (20.0%)

Proteinuria

9 (36.0%)

9 (36.0%)

0 (0.0%)

Abdominal pain

7 (28.0%)

7 (28.0%)

0 (0.0%)

White blood cell decreased

10 (40.0%)

6 (24.0%)

(16.0%)

Anorexia

8 (32.0%)

8 (32.0%)

0 (0.0)

Hyperglycemia

15 (60.0%)

15 (60.0%)

0 (0.0%)

Hyperuricemia

11 (44.0%)

11 (44.0%)

0 (0.0%)

Hypokalemia

10 (40.0%)

10 (40.0%)

0 (0.0%)

Rash

1 (4.0)

1 (4.0)

0 (0.0)

Hypertension

6 (24.0%)

5 (20.0%)

1 (4.0%)

Hand-foot syndrome

14 (56.0%)

13 (56.0%)

0 (0.0)

RCCEP

1 (4.0%)

1 (4.0%)

0 (0.0%)

Diarrhea

2 (8.0%)

2 (8.0%)

0 (0.0%)

Vomiting

2 (8.0%)

2 (8.0%)

0 (0.0%)

Fatigue

14 (56.0%)

14 (56.0%)

0 (0.0%)

Hematuria

 Upper respiratory infection

0 (0.0%)

0 (0.0%)

0 (0.0%)

 Gingival hemorrhage

5 (20.0%)

5 (20.0%)

0 (0.0%)

 Fever

6 (24.0%)

6 (24.0%)

0 (0.0%)

 Oral mucositis

5 (20.0%)

5 (20.0%)

0 (0.0%)

 Gingivitis

5 (20.0%)

5 (20.0%)

0 (0.0%)

 Ascites

4 (16.0%)

0 (0.0%)

0 (0.0%)

 Epistaxis

0 (0.0%)

0 (0.0%)

0 (0.0%)

 Cough

0 (0.0%)

0 (0.0%)

0 (0.0%)

 Headache

0 (0.0%)

0 (0.0%)

0 (0.0%)