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Table 2 Association of expression of PD-L1 to clinicopathological characteristics in 261 patients of lung adenocarcinoma

From: Heterogeneous components of lung adenocarcinomas confer distinct EGFR mutation and PD-L1 expression

 

PD-L1 TPS (%)

p value

< 1%

1–49%

> = 50%

Sex

Male (n = 131)

75 (57.3)

24 (18.3)

32 (24.4)

0.92

Female(n = 130)

72 (55.4)

27 (20.8)

31 (23.8)

 

Clinical stage

I-II (n = 117)

74 (50.3)

23 (45.1)

20 (31.7)

0.04

III + IV (n = 144)

73 (49.7)

28 (54.9)

43 (68.3)

 

LAC predominant components

Acinar

57 (38.8)

15 (29.4)

18 (28.6)

< 0.01

Lepidic

10 (6.8)

3 (5.9)

1 (1.6)

 

Microp

11 (7.5)

4 (7.8)

7 (11.1)

 

Mucinous

10 (6.8)

0 (0)

0 (0)

 

Papillary

39 (26.5)

16 (31.4)

11 (17.5)

 

Solid

20 (13.6)

13 (25.5)

26 (41.3)

 

LACs

With uniform component (n = 114)

71 (48.3)

21 (41.2)

22 (34.9)

0.04*

With two components (n = 104)

53 (36.1)

17 (33.3)

34 (54)

 

With > two components (n = 43)

23 (15.6)

13 (25.5)

7 (11.1)

 

EGFR status

Mutated (n = 154)

84 (57.1)

30 (58.8)

40 (63.5)

0.7

Wild-typed (n = 107)

63 (42.9)

21 (41.2)

23 (36.5)

 
  1. Abbreviations: LAC lung adenocarcinoma, Microp Miropapillary; *P, with some component compared with those without corresponding component