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Table 3 Adverse events (All cycles)

From: Feasibility study of first-line chemotherapy using Pemetrexed and Bevacizumab for advanced or recurrent nonsquamous non-small cell lung cancer in elderly patients: TORG1015

N = 12

CTC-AE grade (Ver. 4.03)

1

2

3

4

3/4 (%)

Leukopenia

1

3

3

0

3 (25 %)

Neutropenia

2

3

3

0

3 (25 %)

Anemia

4

1

1

0

1 (8 %)

Thrombocytopenia

4

0

1

0

1 (8 %)

Febrile Neutropenia

0

0

1

0

1 (8 %)

Hypoalbuminemia

7

1

0

0

0 (0 %)

T-Bil elevation

1

1

0

0

0 (0 %)

AST elevation

6

0

0

0

0 (0 %)

ALT elevation

4

0

0

0

0 (0 %)

ALP elevation

4

0

0

0

0 (0 %)

Cre elevation

3

0

0

0

0 (0 %)

Hyperkalemia

2

0

0

0

0 (0 %)

Hypercalcemia

2

0

0

0

0 (0 %)

Hyponatremia

2

0

0

0

0 (0 %)

Fatigue

3

1

1

0

1 (8 %)

Anorexia

4

3

1

0

1 (8 %)

Weight loss

1

1

0

0

0 (0 %)

Nausea

1

2

1

0

1 (8 %)

Vomiting

2

0

0

0

0 (0 %)

Constipation

2

4

0

0

0 (0 %)

Perforation (colon)

0

0

1

0

1 (8 %)

Hypertension

1

2

0

0

0 (0 %)

Epistaxis

3

0

0

0

0 (0 %)

Stroke

0

1

0

0

0 (0 %)

Urticaria

1

1

0

0

0 (0 %)

Pruritus

2

0

0

0

0 (0 %)

Pneumonitis

2

0

0

0

0 (0 %)

  1. CTC-AE common terminology criteria for adverse events