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. 2023 Nov 24;23:1140. doi: 10.1186/s12885-023-11608-5

Table 4.

Comparison of adverse reactions between the two groups

Adverse reactions Nimotuzumab group(n=52) Control group(n=57) P value
Grade –2(%) Grade 3–4
(%)
Grade 1–2(%) Grade 3–4(%)
Leukopenia 35 (67.3) 1 (1.9) 40 (70.1) 3 (5.3) 0.739
Hemoglobin decreased 20 (38.5) 0 (0.0) 30 (52.6) 0 (0.0) 0.138
Thrombocytopenia 4 (7.7) 0 (0.0) 6 (10.5) 2 (3.5) 0.515
ALT increased 9 (17.3) 0 (0.0) 16 (28.1) 0 (0.0) 0.182
AST increased 2 (3.8) 0 (0.0) 5 (8.8) 0 (0.0) 0.511
Urea increased 2 (3.8) 0 (0.0) 2 (3.5) 0 (0.0) 0.925
Nausea 18 (34.6) 0 (0.0) 17 (29.8) 0 (0.0) 0.593
Vomiting 7 (13.5) 0 (0.0) 11 (19.3) 0 (0.0) 0.412
Oral mucositis 44 (84.6) 8 (15.4) 50 (87.7) 7 (12.3) 0.638
Radiodermatitis 51 (98.1) 1 (1.9) 56 (98.2) 1 (1.8) 1.000
Pharyngeal and esophageal reactions 49 (94.2) 3 (5.8) 56 (98.2) 1 (1.8) 0.546
Weight loss 52 (100.0) 0 (0.0) 57 (100.0) 0 (0.0) -
Hyponatremia 4 (7.7) 0 (0.0) 3 (5.3) 0 (0.0) 0.900
Hypokalemia 17 (32.7) 2 (3.8) 12 (21.1) 2 (3.5) 1.000
Skin rash 1(1.9) 0 (0.0) 0 (0.0) 0 (0.0) -
Infusion reaction 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) -

—is unable to calculate statistics