Table 1 Association between the PD-L1 expression and patient clinicopathological variables.

From: PD-L1 expression as a predictor of postoperative recurrence and the association between the PD-L1 expression and EGFR mutations in NSCLC

Variables

Total

(N = 280)

PD-L1 expression

< 1%

(N = 78)

1–49%

(N = 146)

≥ 50%

(N = 56)

P

Age: ≥ 70 years—no. (%)

156 (55.7)

39 (50.0)

88 (60.3)

29 (51.8)

0.27

Sex: male—no. (%)

157 (56.1)

30 (38.5)

84 (57.5)

43 (76.8)

< 0.001

Current or former smoker—no. (%)

174 (62.1)

40 (51.3)

87 (59.6)

47 (83.9)

< 0.001

Histological type—no. (%)

< 0.001

ADC

216 (77.1)

76 (97.4)

115 (78.7)

25 (44.6)

 

SCC

46 (16.4)

1 (1.3)

22 (15.1)

23 (41.1)

 

Othera

18 (6.4)

1 (1.3)

9 (6.2)

8 (14.3)

 

Pathological stage—no. (%)

< 0.001

I

202 (72.1)

63 (80.8)

109 (74.7)

30 (53.6)

 

II

50 (17.8)

12 (15.4)

23 (15.8)

15 (26.8)

 

IIIA

28 (10.0)

3 (3.8)

14 (9.6)

11 (19.6)

 

Surgical procedure—no. (%)

0.74

Lobectomy

262 (93.6)

76 (97.4)

135 (92.5)

51 (91.1)

 

Bilobectomy

6 (2.1)

1 (1.3)

3 (2.1)

2 (3.6)

 

Lobectomy with combined resection

12 (4.3)

1 (1.3)

8 (5.5)

3 (5.4)

 

Lymph node dissection—no. (%)

< 0.001

ND1

25 (8.9)

17 (21.8)

7 (4.8)

1 (1.8)

 

ND2

255 (91.1)

61 (78.2)

139 (95.2)

55 (98.2)

 

Adjuvant therapy—no. (%)

0.018

Platinum-based chemotherapy

28 (10.0)

4 (5.1)

13 (8.9)

11 (19.6)

 

EGFR mutation—no. (%)

< 0.001

Wild-type

181 (64.6)

38 (48.7)

92 (63.0)

51 (91.1)

 

Ex21

48 (17.1)

19 (24.4)

28 (19.2)

1 (1.8)

 

Ex19

31 (11.1)

15 (19.2)

14 (9.6)

2 (3.6)

 

Minor mutationb

20 (7.1)

6 (7.7)

12 (8.2)

2 (3.6)

 
  1. PD-L1 programmed cell death-ligand 1, ADC adenocarcinoma, SCC squamous cell carcinoma, EGFR epidermal growth factor receptor gene, Ex21 exon 21 L858R mutation, Ex19 exon19 deletion mutation.
  2. aDefined as histological types of NSCLC with the exclusion of ADC and SCC. Of 18 cases, 2 patients with large cell carcinoma, 3 patients with adenosquamous carcinoma, 7 patients with large cell neuroendocrine carcinoma and 6 patients with pleomorphic carcinoma.
  3. bDefined as all mutations except Ex21 and Ex19.