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. 2020 Jan 31;20:83. doi: 10.1186/s12885-020-6579-z

Table 1.

Demographic and clinicopathologic characteristics in the development cohort

Variable Value
Sex, n (%)
 Male 132 (46.6)
 Female 151 (53.4)
Age, median (range) 65.4 y (27.5–90.2 y)
Race/ethnicity, n (%)
 Caucasian 215 (76.0)
 Asian 27 (9.5)
 Black 19 (6.7)
 Hispanic 21 (7.4)
 Unknown 1 (0.3)
Smoking status, n (%)
 Never-smoker 64 (22.6)
 Former smoker 136 (48.1)
 Current smoker 82 (29.0)
 Unknown 1 (0.3)
Vital status, n (%)
 Alive 172 (60.8)
 Deceased 111 (39.2)
Molecular platform, n (%)
 NGS 218 (77.0)
 PCRa 55 (19.5)
 Not done 10 (3.5)
Molecular subtype, n (%) (n = 233)
 sTRU – EGFR (%) 34 (14.6)
 sPP – KRAS (%) 43 (18.5)
 sPI – TP53 (%) 46 (19.7)
 Co-mutation 60 (25.8)
EGFR/TP53 26 (11.2)
KRAS/ TP53 34 (14.6)
 Non-TRUPPPI 21 (9.0)
 No mutations detected by NGS 29 (12.4)
FISH results, n (%)
 Negative 250 (88.3)
 Positive 24 (8.5)
ALK 16 (5.7)
ROS1 1 (0.4)
RET 2 (0.7)
MET 5 (1.8)
 Indeterminate 9 (3.2)
 Aneuploidy 193 (68.2)

NGS Next-generation sequencing, PCR Polymerase chain reaction, sTRU Simplified terminal respiratory unit, sPP Simplified proximal-proliferative, sPI Simplified proximal-inflammatory, non-TRUPPPI Mutations in genes other than EGFR, KRAS, and TP53, FISH Fluorescence in situ hybridization

aSanger sequencing or pyrosequencing