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. 2019 Jan 14;53(2):86–93. doi: 10.4132/jptm.2018.12.26

Table 1.

Clinicopathologic characteristics

Characteristic No. (%)
Age (yr)
 Median (range) 65 (23–82)
Sex
 Male 191 (47.4)
 Female 212 (52.6)
Smoking statusa
 Never 242 (60.0)
 Ex-smoker 89 (22.1)
 Current 72 (17.9)
Differentiationb
 Well differentiated 34 (8.4)
 Moderately differentiated 315 (78.2)
 Poorly differentiated 54 (13.4)
Genetic statusc
EGFR mutant 192 (69.1)
ALK mutant 20 (7.2)
KRAS mutant 16 (5.8)
EGFR(–)/ALK(–)/KRAS(–) 50 (18.0)
Tumor size (cm)
 Mean (range) 31.7 (0.8–16.0)
Pleural invasion
 Absent 235 (58.3)
 Present 168 (41.7)
Venous invasion
 Absent 302 (74.9)
 Present 101 (25.1)
Lymphatic invasion
 Absent 213 (52.9)
 Present 190 (47.1)
Perineural invasion
 Absent 380 (94.3)
 Present 23 (5.7)
Pathologic stage
 IA 127 (31.5)
 IB 107 (26.6)
 IIA 64 (15.9)
 IIB 19 (4.7)
 IIIA 77 (19.1)
 IIIB 9 (2.2)
HLA class I IHC (%)
 < 25 249 (61.8)
 25–74 120 (29.8)
 ≥ 75 34 (8.4)
PD-L1 IHC (%)
 < 1 338 (83.9)
 1–49 42 (10.4)
 ≥ 50 23 (5.7)
Total 403 (100)

EGFR, epidermal growth factor receptor; ALK, anaplastic lymphoma kinase; HLA, human leukocyte antigen; IHC, immunohistochemistry; PD-L1, programmed death-ligand 1.

a

Smoking status was defined as follows: never smoker (< 100 cigarettes per lifetime); ex-smoker (≥ 100 cigarettes per lifetime and quit > 1 year prior to the diagnosis); current smoker (≥ 100 cigarettes per lifetime and smoked at the time of lung cancer diagnosis or quit ≤ 1 year prior to the diagnosis);

b

Differentiation was defined as follows: well differentiated (lepidic predominant); moderately differentiated (acinar or papillary predominant); poorly differentiated (micropapillary or solid predominant);

c

Genetic status was evaluable for 278 patients.