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Table 2 Summary of treatment-related adverse events

From: Intensive cycles of neoadjuvant camrelizumab combined with chemotherapy in locally advanced esophageal squamous cell carcinoma: a single-arm, phase II trial

All events

No. of patients (%)

Total

Grade 1–2

Grade 3–4

Alopecia

32 (68.1)

32 (68.1)

0 (0)

Reactive cutaneous capillary endothelial proliferation

28 (59.6)

28 (59.6)

0 (0)

Fatigue

26 (55.3)

25 (53.2)

1 (2.1)

Anemia

25 (53.2)

24 (51.1)

1 (2.1)

Muscle soreness

20 (42.6)

20 (42.6)

0 (0)

Limb numbness

20 (42.6)

19 (40.4)

1 (2.1)

Increased alanine transaminase

11 (23.4)

11 (23.4)

0 (0)

Constipation

8 (17.0)

8 (17.0)

0 (0)

Diarrhea

4 (8.5)

4 (8.5)

0 (0)

Immune-related hyperthyroidism

4 (8.5)

4 (8.5)

0 (0)

Leukopenia

3 (6.4)

3 (6.4)

0 (0)

Vomiting

2 (4.3)

2 (4.3)

0 (0)

Nausea

2 (4.3)

2 (4.3)

0 (0)

Immune-related hypothyroidism

2 (4.3)

2 (4.3)

0 (0)

Thrombocytopenia

2 (4.3)

2 (4.3)

0 (0)

Immune-related myocarditis

1 (2.1)

0 (0)

1 (2.1)

Cough

0 (0)

0 (0)

0 (0)

Immune-related pneumonia

0 (0)

0 (0)

0 (0)

Immune-related hepatitis

0 (0)

0 (0)

0 (0)

Immune-related nephritis

0 (0)

0 (0)

0 (0)

  1. All adverse events were reported according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0