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. 2018 Mar 8;9(1):13–20. doi: 10.14740/wjon1084w

Table 2. Treatment and Efficacy.

All, N = 159 LMR
mGPS
< 1.97, N = 24 ≥ 1.97, N = 135 P 0 - 1, N = 120 2, N = 39 P
First-line regimen
  Single or combination (N)
    Single/combination 4/155 0/24 4/131 1.00a 4/116 0/39 0.57a
  Platinum-based (N)
    CDDP/CBDCA 52/103 8/16 44/87 1.00a 43/73 9/30 0.12a
  PEM-containing (N) 77 13 64 0.66a 59 18 0.85a
  Bev-containing (N) 32 4 28 0.79a 23 9 0.65a
  Concurrent TRT (N) 8 0 8 0.61a 6 2 1.00a
First-line response
  RR (%) (95% CI) 40.9 (33.2 - 48.9) 8.3 (1.0 - 27.0) 46.7 (38.0 - 55.4) < 0.01a 45.0 (35.9 - 54.3) 28.2 (15.0 - 44.9) 0.09a
  DCR (%) (95% CI) 69.8 (62.0 - 76.8) 33.3 (15.6 - 55.3) 76.3 (68.2 - 83.2) < 0.01a 76.7 (68.1 - 83.9) 48.7 (32.4 - 65.2) < 0.01a
  PFS (months) (95% CI) 5.4 (4.6 - 6.3) 2.7 (1.0 - 3.7) 5.7 (5.3 - 6.6) < 0.01b 5.7 (5.2 - 6.8) 3.1 (1.6 - 5.3) 0.01b
Second or further line (N) 96 5 91 < 0.01a 84 12 < 0.01a
  ICI (N) 20 1 19 0.31a 18 2 0.16a

aFisher’s exact test. bLog-rank test. Bev: bevacizumab; CBDCA: carboplatin; CDDP: cisplatin; CI: confidence interval; DCR: disease control rate; ICI: immuno-checkpoint inhibitor; LMR: lymphocyte to monocyte ratio; mGPS: modified Glasgow prognostic score; PEM: pemetrexed; PFS: progression-free survival; RR: response rate; TRT: thoracic radiotherapy.