Table 3 Treatment-related adverse events

From: Neoadjuvant camrelizumab (an anti-PD-1 antibody) plus chemotherapy or apatinib (a VEGFR-2 inhibitor) for initially unresectable stage II–III non-small-cell lung cancer: a multicentre, two-arm, phase 2 exploratory study

Events, n (%)a

Arm A (n = 30)

Arm B (n = 21)

Any grade

Grade ≥ 3

Any grade

Grade ≥ 3

Any

24 (80.0)

8 (26.7)

18 (85.7)

3 (14.3)

White blood cell count decreased

10 (33.3)

2 (6.7)

0

0

Anemia

9 (30.0)

2 (6.7)

2 (9.5)

0

Alanine aminotransferase increased

9 (30.0)

1 (3.3)

3 (14.3)

2 (9.5)

Neutrophil count decreased

8 (26.7)

5 (16.7)

1 (4.8)

0

Platelet count decreased

8 (26.7)

3 (10.0)

0

0

Gamma-glutamyltransferase increased

8 (26.7)

1 (3.3)

3 (14.3)

0

Aspartate aminotransferase increased

5 (16.7)

0

3 (14.3)

1 (4.8)

Alkaline phosphatase increased

3 (10.0)

1 (3.3)

1 (4.8)

0

Pruritus

2 (6.7)

0

1 (4.8)

0

Proteinuria

2 (6.7)

0

2 (9.5)

0

Lymphocyte count decreased

2 (6.7)

0

0

0

Reactive cutaneous capillary endothelial proliferation

1 (3.3)

0

5 (23.8)

0

Blood bilirubin increased

1 (3.3)

0

1 (4.8)

1 (4.8)

Autoimmune hepatitis

1 (3.3)

1 (3.3)

0

0

Hyperuricemia

0

0

3 (14.3)

0

Blood glucose increased

0

0

3 (14.3)

0

Blood lactate dehydrogenase increased

0

0

2 (9.5)

0

  1. aData presented for treatment-related adverse events (TRAEs) occurring in at least 5% of patients, or any TRAEs of grade 3 or above in either arm