Skip to main content

Table 3 Treat-related adverse events (n = 52)

From: Nimotuzumab combined with docetaxel and cisplatin as first-line treatment for patients with recurrent or metastatic nasopharyngeal carcinoma: a multicenter, phase 2 trial

TRAEs

All grades

Grade 1–2

Grade 3 or more

Neutropenia

29 (55.8%)

7 (13.5%)

22 (42.3%)

Leukopenia

30 (57.7%)

13 (25.0%)

17 (32.7%)

Febrile neutropenia

6 (11.5%)

0

6 (11.5%)

Thrombocytopenia

11 (21.2%)

10 (19.2%)

1 (1.9%)

Anemia

41 (78.8%)

41 (78.8%)

0

Nausea

19 (36.5%)

15 (28.8%)

4 (7.7%)

Fatigue

13 (25.0%)

10 (19.2%)

3 (5.8%)

Infection

4 (7.7%)

1 (1.9%)

3 (5.8%)

Anorexia

6 (11.5%)

5 (9.6%)

1 (1.9%)

Oral ulcers

3 (5.8%)

2 (3.8%)

1 (1.9%)

Hypertriglyceridemia

20 (38.5%)

20 (38.5%)

0

Hypercholesterolemia

20 (38.5%)

20 (38.5%)

0

Hyperglycemia

14 (26.9%)

14 (26.9%)

0

Limb numbness

14 (26.9%)

14 (26.9%)

0

Creatinine elevated

11 (21.2%)

11 (21.2%)

0

Rash

11 (21.2%)

11 (21.2%)

0

ALT elevated

10 (19.2%)

10 (19.2%)

0

Diarrhea

8 (15.4%)

8 (15.4%)

0

Hypertension

6 (11.5%)

6 (11.5%)

0

AST elevated

6 (11.5%)

6 (11.5%)

0

Edema

4 (7.7%)

4 (7.7%)

0

Alopecia

3 (5.8%)

3 (5.8%)

0

Otitis

2 (3.8%)

2 (3.8%)

0

Hyperkalemia

2 (3.8%)

2 (3.8%)

0

Pigmentation

1 (1.9%)

1 (1.9%)

0

Dyspnea

1 (1.9%)

1 (1.9%)

0

  1. Data are shown as number (%)
  2. Abbreviations: ALT Alanine aminotransferase, AST Aspartate aminotransferase, TRAEs Treat-related adverse events