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Table 2 Summary of adverse events

From: S-1 plus cisplatin with concurrent radiotherapy versus cisplatin alone with concurrent radiotherapy for stage III non-small cell lung cancer: a pilot randomized controlled trial

Adverse events

SCCR (n = 20)

CCR (n = 20)

G3/4 (≥G3) (%)

G3/4 (≥G3) (%)

Haematolgic

  Leukopenia

4/1 (25.0%)

3/1 (20.0%)

  Thrombocytopenia

4/0 (20.0%)

3/1 (20.0%)

  Neutropenia

4/0 (20.0%)

3/0 (15.0%)

  Febrile neutropenia

3/0 (15.0%)

3/0 (15.0%)

  Anaemia

3/0 (15.0%)

2/0 (10.0%)

Non-haematolgic

  Anorexia

3/0 (15.0%)

2/0 (10.0%)

  Nausea

1/1 (10.0%)

2/0 (10.0%)

  Constipation

2/0 (10.0%)

2/0 (10.0%)

  Oesophagitis

2/0 (10.0%)

1/0 (5.0%)

  Fatigue

1/0 (5.0%)

2/0 (10.0%)

  ALT, AST

1/0 (5.0%)

0/0 (0%)

  Pneumonitis

1/0 (5.0%)

0/0 (0%)

  Diarrhoea

0/0 (0%)

1/0 (5.0%)