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. 2020 Nov 27;112(1):72–80. doi: 10.1111/cas.14705

TABLE 1.

Clinical characteristics

All (n = 68) PD‐L1 high (n = 27) PD‐L1 low (n = 41) P value
n (%) n (%) n (%)
Age (y), median (range) 70 (31, 91) 70 (55, 91) 71 (31, 85) .405
Gender
Male 51 (75) 22 (85) 29 (71) .310
Female 17 (25) 5 (19) 12 (29)
Smoking status, n (%)
Never 11 (16) 2 (7) 9 (22) .602
Ex or current 57 (84) 25 (93) 32 (78)
PS
0‐1 52 (76) 23 (85) 29 (71) .160
2 16 (24) 4 (15) 12 (29)
Histology
Squamous cell 24 (35) 8 (30) 16 (39) .682
Adenocarcinoma 38 (56) 16 (59) 22 (54)
Others 6 (9) 3 (11) 3 (7)
Previous chemotherapy
0 26 (38) 22 (81) 4 (10) <.001*
1 27 (40) 3 (11) 24 (59)
>2 15 (22) 2 (7) 13 (32)
Treatment
Nivolumab 26 (38) 2 (7) 24 (59) <.001*
Pembrolizumab 33 (49) 24 (89) 9 (22)
Atezolizumab 9 (13) 1 (4) 8 (20)
Stage
III 11 (16) 3 (11) 8 (20) .333
IV 38 (56) 18 (67) 20 (49)
Recurrence 19 (28) 6 (22) 13 (32)
PD‐L1 tumor expression
High (≥50%) 27 (40) 27 (100) 0
Low (<50%) 41 (60) 0 41 (100)
Gene alterations
WT 39 (57) 18 (67) 21 (51) .116
EGFR 5 (7) 0 5 (12)
ALK 2 (3) 1 (4) 1 (2)
NE 22 (32) 8 (30) 14 (34)

Abbreviations: ALK, anaplastic lymphoma kinase; EGFR, epidermal growth factor receptor; NE, not examined; PD‐L1, programmed death–ligand 1; PS, East Cooperative Oncology Group performance status; WT, wild type.

*

P < .05.