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Table 2 Adverse events (grades 1 and 2)

From: Immuno-priming durvalumab with bevacizumab in HER2-negative advanced breast cancer: a pilot clinical trial

Event

Grade 1

Grade 2

Total

Asthenia

4 (16%)

1 (4%)

5 (20%)

Headache

2 (8%)

1 (4%)

3 (12%)

Proteinuria

2 (8%)

0 (0%)

2 (8%)

Hypertension

1 (4%)

1 (4%)

2 (8%)

Diarrhea

2 (8%)

0 (0%)

2 (8%)

Pruritus

0 (0%)

1 (4%)

1 (4%)

Hyporexia

0 (0%)

1 (4%)

1 (4%)

Nausea

0 (0%)

1 (4%)

1 (4%)

Pneumonitis

0 (0%)

1 (4%)

1 (4%)

Thrombosis

0 (0%)

1 (4%)

1 (4%)

Infection

0 (0%)

1 (4%)

1 (4%)

Elevated amylase

1 (4%)

0 (0%)

1 (4%)

Elevated lipase

1 (4%)

0 (0%)

1 (4%)

Rash

1 (4%)

0 (0%)

1 (4%)

Xerosis

1 (4%)

0 (0%)

1 (4%)

Hypothyroidism

1 (4%)

0 (0%)

1 (4%)

Abdominal pain

1 (4%)

0 (0%)

1 (4%)

Vomiting

1 (4%)

0 (0%)

1 (4%)

Pyrexia

1 (4%)

0 (0%)

1 (4%)

Arthralgia

1 (4%)

0 (0%)

1 (4%)

Xerophtalmia

1 (4%)

0 (0%)

1 (4%)