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. 2021 Apr 28;9(2):471–488. doi: 10.1007/s40487-021-00150-8

Table 2.

Demographic and clinical characteristics of the analytical cohort by histology

Baseline characteristics Histology
Overall Non-squamousa Squamous Not otherwise specified
n %b n %b n %b n %b
81,628 100% 46,670 57% 21,540 26% 13,418 16%
Year of diagnosis
 2008 2535 3.1% 1125 2.4% 613 2.8% 797 5.9%
 2009 3781 4.6% 1809 3.9% 998 4.6% 974 7.3%
 2010 5186 6.4% 2566 5.5% 1362 6.3% 1258 9.4%
 2011 6575 8.1% 3455 7.4% 1533 7.1% 1587 11.8%
 2012 8037 9.8% 4334 9.3% 1966 9.1% 1737 12.9%
 2013 9423 11.5% 5275 11.3% 2483 11.5% 1665 12.4%
 2014 10254 12.6% 5909 12.7% 2674 12.4% 1671 12.5%
 2015 10077 12.3% 6072 13.0% 2740 12.7% 1265 9.4%
 2016 9870 12.1% 6097 13.1% 2696 12.5% 1077 8.0%
 2017 8948 11.0% 5590 12.0% 2523 11.7% 835 6.2%
 2018 6942 8.5% 4438 9.5% 1952 9.1% 552 4.1%
Gender
 Male 39987 49.0% 20762 44.5% 12722 59.1% 6503 48.5%
 Female 41599 51.0% 25885 55.5% 8809 40.9% 6905 51.5%
 Unknown 42 0.1% 23 0.0% 9 0.0% 10 0.1%
Region
 Midwest 38317 46.9% 21450 46.0% 10708 49.7% 6159 45.9%
 South 23171 28.4% 13070 28.0% 6445 29.9% 3656 27.2%
 West 7559 9.3% 4671 10.0% 1828 8.5% 1060 7.9%
 Northeast 10380 12.7% 6263 13.4% 1974 9.2% 2143 16.0%
Other/Unknown 2201 2.7% 1216 2.6% 585 2.7% 400 3.0%
Race
 Caucasian 69138 84.7% 38996 83.6% 18659 86.6% 11483 85.6%
 African American 7270 8.9% 4385 9.4% 1795 8.3% 1090 8.1%
 Asian 1164 1.4% 869 1.9% 137 0.6% 158 1.2%
 Other/unknown 4056 5.0% 2420 5.2% 949 4.4% 687 5.1%
Ethnicity
 Non-Hispanic 73931 90.6% 42329 90.7% 19718 91.5% 11884 88.6%
 Hispanic 1507 1.8% 970 2.1% 320 1.5% 217 1.6%
 Unknown 6190 7.6% 3371 7.2% 1502 7.0% 1317 9.8%
Age at diagnosis (in years)
 Mean (SD) 69.1 (10.12) 68.5 (10.44) 70.3 (9.32) 69.4 (10.02)
 Median (IQR) 70 (62–77) 69 (61–77) 71 (64–78) 70 (63–77)
 Min–Max (18–89) (18–89) (23–89) (21–89)
  ≤ 34 117 0.1% 89 0.2% 11 0.1% 17 0.1%
 35–44 835 1.0% 614 1.3% 92 0.4% 129 1.0%
 45–54 6161 7.5% 4004 8.6% 1151 5.3% 1006 7.5%
 55–64 18797 23.0% 11475 24.6% 4423 20.5% 2899 21.6%
 65+ 55718 68.3% 30488 65.3% 15863 73.6% 9367 69.8%
ECOG score
 Index ± 30 days
  0 3054 28.8% 2201 31.5% 701 23.5% 152 23.9%
  1 4372 41.2% 2866 41.0% 1261 42.3% 245 38.5%
  2 1909 18.0% 1143 16.3% 633 21.3% 133 20.9%
  3 1010 9.5% 630 9.0% 301 10.1% 79 12.4%
  4 262 2.5% 155 2.2% 80 2.7% 27 4.2%
  5 4 0.0% 2 0.0% 2 0.1% 0 0.0%
  Missing 71017 39673 18562 12782 -
Stage
 Index through follow-up (localized unknown) ± 30 days (locally advanced metastatic)
  Localized (stage ≤ 3a) 20425 59.4% 13103 54.0% 6807 70.6% 515 100.0%
  Locally advanced/metastasis (≥ 3b) 13973 40.6% 11142 46.0% 2831 29.4% 0 0.0%
  Unknown 24516 11395 6270 6851
  Missing 22714 11030 5632 6052
Cytogenetics
 Any time
  EGFR-positivec 9267 38.3% 8208 44.6% 704 15.6% 355 27.2%
  EGFR-negative 5575 23.0% 4303 23.4% 988 22.0% 284 21.7%
  PD-L1–positive 1933 8.0% 1140 6.2% 730 16.2% 63 4.8%
  PD-L1–negative 487 2.0% 354 1.9% 122 2.7% 11 0.8%
  Both 448 1.8% 399 2.2% 38 0.8% 11 0.8%
  Other 6510 26.9% 4010 21.8% 1917 42.6% 583 44.6%
  Missing 57408 28256 17041 12111 -
 Charlson comorbidityd n = 81778 n = 38455 n = 18004 n = 6715
  Mean (SD) 1.8 (2.56) 2 (2.74) 1.7 (2.34) 1.4 (2.22)
  Median 1 (0–3) 1 (0–3) 1 (0–2) 0 (0–2)
  Min–Max (0–16) (0–15) (0–16) (0–14)

ECOG Eastern Cooperative Oncology Group; EGFR epidermal growth factor receptor; PD-L1 programmed death-ligand 1; IQR interquartile range; SD standard deviation

aPatients with squamous cell carcinoma were compared against patients with non-squamous cell carcinoma only; non-squamous NSCLC includes adenocarcinoma and large cell lung cancer; patients with unknown histology were excluded from this analysis

bPercentages are based on non-missing values in respective cohort

cA patient was EGFR-mutant if identified as EGFR-positive from the SDS data set or had received osimertinib, erlotinib, afatinib, gefitinib or dacomitinib (monotherapy or in combination with chemotherapy drugs) in LOT1. Chemotherapy drugs: Carboplatin, cisplatin, docetaxel, gemcitabine, nab-paclitaxel, paclitaxel, pemetrexed, or vinorelbine

dComorbidities identified during the 180-day pre-index period