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Table 3 Incidence, severity, treatment and outcomes of patients who had irAEs

From: Patterns and outcomes of immune-related adverse events in solid tumor patients treated with immune checkpoint inhibitors in Thailand: a multicenter analysis

irAEs

Grade (n = 414)

Median onset,days (range)

Median Time to Resolution, days (range)

irAE specific Treatment (n, %)

Termination of ICI due to irAE (n, %)

irAE Recovery (n, %)

ICI rechallenge (n, %)

Recurrence of irAE after rechallenge (n, %)

All

Gr 1–2

Gr 3–5

Overall

98 (23.7)

75 (18.1)

23 (5.6)

63 (1–526)

51 (1–951)

56/98 (57.1)

22/98 (22.5)

84/98 (85.7)

68/98 (69.4)

11/68 (11.2)

Endocrine

 Hypothyroid

31 (7.5)

31 (7.5)

–

112 (19–574)

168 (11–804)

25/31 (80.7)

5/31 (16.1)

25/31 (80.7)

21/31 (67.7)

1/21 (4.8)

 Hyperthyroid

11 (2.7)

11 (2.7)

–

47 (15–203)

35 (12–751)

6/11 (54.6)

0

10/11 (90.9)

8/11 (72.7)

0/8

 Hypophysitis

5 (1.2)

4 (1.0)

1 (0.2)

178 (1–348)

208 (54–807)

5/5 (100)

1/5 (20.0)

5/5 (100)

4/5 (80.0)

0/4

GI

 Colitis

1 (< 0.01)

–

1 (< 0.01)

475

181

1

0

1

1

0

 Hepatitis

27 (6.5)

22 (5.3)

5 (1.2)

42 (7–400)

42 (7–632)

5/27 (18.5)

8/27 (29.6)

23/27 (85.2)

17/27 (63.0)

3/17 (17.7)

 Pancreatitis

11 (2.7)

9 (2.2)

2 (0.5)

30 (14–254)

84 (1–707)

1/11 (9.1)

1/11 (9.1)

9/11 (81.8)

10/11 (90.9)

4/10 (40.0)

Lung

 Pneumonitis

6 (1.4)

3 (0.7)

3 (0.7)

34 (23–139)

18.5 (8–33)

5/6 (83.3)

2/6 (33.3)

6/6 (100)

3/6 (50.0)

0/3

Skin

 Rash

20 (4.8)

17 (4.1)

3 (0.7)

55.5 (3–420)

34 (7–253)

14/20 (70.0)

4/20 (20.0)

18/20 (90.0)

17/20 (85.0)

4/17 (23.5)

 Vitiligo

1 (< 0.01)

1 (< 0.01)

–

70

951

1

0

0

1

1

Others

 Others

8 (2.0)

4 (1.0)

4 (1.0)

181.5 (2–505)

31.5 (20–86)

4/8 (50.0)

2/8 (25.0)

7/8 (87.5)

4/8 (50.0)

0/4

  1. Gr grade, irAE immune related adverse events, ICI immune checkpoint inhibitor, GI gastrointestinal adverse events, n number of patients