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Table 2 Newly diagnosed cardiovascular disease after ICI initiation

From: Newly diagnosed cardiovascular disease in patients treated with immune checkpoint inhibitors: a retrospective analysis of patients at an academic tertiary care center

Immune Checkpoint Inhibitor

Cardiomyopathy, n (%)

Heart failure, n (%)

Arrhythmia, n (%)

Pericardial disease, n (%)

Heart block, n (%)

Myocarditis, n (%)

Any cardiotoxicity, n (%)

Median (IQR) time to cardiotoxicity, days

PD-1 inhibitors

 nivolumab (n = 217)

1 (0.46)

10 (4.61)

15 (6.91)

7 (3.23)

6 (2.76)

1 (0.46)

33 (15.21)

52 (37–203)

 pembrolizumab (n = 123)

0

6 (4.88)

3 (2.44)

1 (0.81)

1 (0.81)

0

11 (8.94)

65 (30–175)

PD-L1 inhibitors

 atezolizumab (n = 17)

0

1 (5.88)

2 (11.76)

0

0

0

3 (17.65)

22 (2–172)

 durvalumab (n = 4)

1 (25)

0

0

0

0

0

1 (25.00)

30

CTLA-4 inhibitor

 ipilimumab (n = 13)

0

4 (30.77)

1 (7.69)

0

1 (7.69)

0

6 (46.15)

709 (78–1469)

CTLA-4 + PD-1/PD-L1 inhibitor combination

 ipilimumab + nivolumab (n = 29)

2 (6.9)

1 (3.45)

4 (13.79)

0

1 (3.45)

0

7 (24.14)

95 (11–119)

 ipilimumab + pembrolizumab (n = 7)

0

1 (14.29)

1 (14.29)

0

0

0

1 (14.29)

62

 tremelimumab + durvalumab (n = 3)

0

0

0

0

0

0

0

 

PD-1/PD-L1 dual sequential

 nivolumab - > pembrolizumab (n = 4)

0

0

0

0

0

0

0

 

 nivolumab - > atezolizumab (n = 3)

0

0

0

0

0

0

0

 

 pembrolizumab - > atezolizumab (n = 3)

0

0

0

0

0

0

0

 

Three-drug sequential

 ipilimumab + nivolumab - > pembrolizumab (n = 1)

0

0

0

0

0

0

0

 

Total (n = 424)

4 (0.94)

23 (5.42)

26 (6.13)

8 (1.89)

9 (2.12)

1 (0.24)

62 (14.62)

63 (30–175)

  1. IQR inter-quartile range