Skip to main content

Table 6 AEs in advanced NSCLC patients who received combination therapy with PD-1 inhibitors and antiangiogenic agents

From: Efficacy and safety of combined immunotherapy and antiangiogenic therapy for advanced non-small cell lung cancer: a real-world observation study

Adverse events

Any Grade n (%)

 ≥ Grade 3(n/%)

Fatigue

28(32.9)

1(1.2)

Proliferation of capillaries

27(31.8)

0(0)

Hypertension

25(29.4)

4(4.7)

Proteinuria

23(27.1)

3(3.5)

Abnormal thyroid function

22(25.9)

2(2.4)

Hand-foot syndrome

20(23.5)

3(3.5)

Rash

18(21.2)

3(3.5)

Anorexia

17(20)

0(0)

Dyslipidaemia

15(17.6)

1(1.2)

Thrombocytopenia

14(16.5)

3(3.5)

Hepatic dysfunction

13(15.3)

2(2.4)

Oedema

12(14.1)

1(1.2)

Anaemia

11(12.9)

1(1.2)

Diarrhoea

11(12.9)

0(0)

Haemorrhage

10(11.8)

0(0)

Nausea

10(11.8)

0(0)

Pruritus

9(10.6)

1(1.2)

Oral mucositis

8(9.4)

0(0)

Myalgia

7(8.2)

0(0)

Leukopenia

6(7.1)

1(1.2)

Pneumonitis

5(5.9)

1(1.2)

Hypophysitis

2(2.4)

0(0)

Myocarditis

2(2.4)

1(1.2)

Encephalitis

1(1.2)

0(0)

  1. AEs Treatment-related adverse events, NSCLC Non-small cell lung cancer, PD-1 Programmed death 1