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. 2018 Feb 15;15(4):5671–5679. doi: 10.3892/ol.2018.8064

Table I.

Baseline clinical characteristics for patients in the chemotherapy-bevacizumab group vs. chemotherapy alone group prior and subsequent to propensity score matching.

A, Unmatched dataset

Characteristics Chemotherapy-bevacizumab (n=43) Chemotherapy alone (n=122) P-value
Age, years 0.844
  Median (range) 52 (37–72) 56 (27–76)
  ≤60 32 88
  >60 11 34
Sex, n 0.287
  Male 19 67
  Female 24 55
Smoking history, n 0.583
  Current/previous 14 47
  Never 29 75
Histology, n 0.800
  Adenocarcinoma 38 105
  Squamous cell/adenosquamous carcinoma 5 17
EGFR mutation status 0.716
  Mutant typea 17 44
  Wild-type/unknown 26 78
Number of prior regimensb, n 0.009
  Median (range) 3 (2–5) 2 (2–5)
  ≤3 28 103
  >3 15 19
Chemotherapy regimen, n <0.0001
  Gemcitabine 30 39
  Pemetrexed 5 31
  Paclitaxel 3 8
  Docetaxel 5 44

B, Matched (1:1) dataset

Characteristics Chemotherapy-bevacizumab (n=38) Chemotherapy alone (n=38) P-value

Age, years 1.000
  Median (range) 52 (40–71) 49 (38–76)
  ≤60 30 31
  >60 8
Sex 0.492
  Male 17 21
  Female 21 17
Smoking history, n 0.240
  Current/previous 26 20
  Never 12 18
Histology, n 1.000
  Adenocarcinoma 34 35
  Squamous cell/ 4 3
  adenosquamous carcinoma
EGFR mutation status 0.641
  Mutant typea 17 14
  Wild-type/unknown 21 24
Number of prior regimensb, n 1.000
  Median (range) 3 (2–5) 3 (2–4)
  ≤3 28 28
  >3 10 10
Chemotherapy regimen, n 1.000
  Gemcitabine 25 25
  Pemetrexed 5 5
  Paclitaxel 3 3
  Docetaxel 5 5

EGFR, epidermal growth factor receptor.

a

Mutant type included the exon 19 deletion and exon 21 L858R mutations.

b

Prior regimens included chemotherapy, EGFR tyrosine kinase inhibitors and anaplastic lymphoma kinase inhibitors.