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Table 3 Treatment-related adverse events during anti-PD(L)-1 and anti-tuberculosis treatment (N=45)

From: Assessment of anti-PD-(L)1 for patients with coexisting malignant tumor and tuberculosis classified by active, latent, and obsolete stage

TRAEs

Any grade

Grade 1

Grade 2

Grade 3-5

Any event

33 (73.3)

12 (26.7)

15 (33.3)

6 (13.3)

Hematotoxicity

27 (60)

8 (17.8)

14 (31.1)

5 (11.1)

Hepatic toxicity

4 (8.9)

3 (6.7)

1 (2.2)

0

Pneumonitis

1 (2.2)

0

0

1 (2.2)

Gastrointestinal toxicity

2 (4.4)

2 (4.4)

0

0

Rash

4 (8.9)

3 (6.7)

1 (2.2)

0

Fatigue

3 (6.7)

2 (4.5)

1 (2.2)

0

Endocrine toxicity

1 (2.2)

1 (2.2)

0

0

Cardiovascular toxicity

0

0

0

0

Any event leading to discontinuation of ICI

1 (2.2)

0

0

1 (2.2)

Any event leading to death

0

0

0

0

  1. Abbreviation: TRAEs Treatment-related adverse events, ICI immune checkpoint inhibitors