Table 3 Summary of adverse events by preferred terms (30-day safety window).

From: A Phase 2 study of nivolumab in combination with modified FOLFIRINOX for metastatic pancreatic cancer

Adverse event preferred term

Any grade

Grade 3/4

Nausea

25 (80.6)

3 (9.7)

Diarrhoea

19 (61.3)

1 (3.2)

Neutrophil count decreased

19 (61.3)

12 (38.7)

Peripheral sensory neuropathy

19 (61.3)

0

Decreased appetite

18 (58.1)

5 (16.1)

Stomatitis

15 (48.4)

0

Constipation

13 (41.9)

0

Dysgeusia

12 (38.7)

0

Malaise

14 (45.2)

1 (3.2)

Rash

10 (32.3)

1 (3.2)

White blood cell count decreased

9 (29.0)

3 (9.7)

Platelet count decreased

8 (25.8)

0

Alopecia

7 (22.6)

0

Fatigue

7 (22.6)

0

Hiccups

7 (22.6)

0

Pyrexia

7 (22.6)

0

  1. Data are presented as n (%) for adverse events observed in ≥20% of the patients between the first day of the regimen and 30 days after the last dose.
  2. There were no Grade 5 adverse events.