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. 2021 Sep;10(9):3782–3792. doi: 10.21037/tlcr-21-681

Table 1. Baseline demographic and clinical characteristics of patients stratified by treatment strategies after TKI resistance (n=144).

Characteristics Total (n=144) Chemo + IO (n=44) Chemo + antiangiogenesis (n=100) P value
Age, years, median [range] 61 [19–76] 63.5 [19–76] 58.5 [36–75] 0.001
Gender, n (%) 0.421
   Male 68 (47.2) 23 (52.3) 45 (45.0)
   Female 76 (52.8) 21 (47.7) 55 (55.0)
Smoking status, n (%) 0.554
   Current/former 34 (23.6) 9 (20.5) 25 (25.0)
   Never 110 (76.4) 35 (79.5) 75 (75.0)
EGFR subtypes, n (%) 0.229
   19Del 77 (53.5) 22 (50.0) 55 (55.0)
   L858R 51 (35.4) 20 (45.5) 31 (31.0)
   Rare mutationsa 13 (9.0) 2 (4.5) 11 (11.0)
   Unknown 3 (2.1) 0 (0) 3 (3.0)
PD-L1 status, n (%) 0.604
   ≥1% 6 (4.2) 3 (6.8) 3 (3.0)
   <1% 6 (4.2) 2 (4.5) 4 (4.0)
   Not examined 132 (91.7) 39 (88.6) 93 (93.0)
No. of metastatic sites, n (%) 0.069
   0–1 71 (49.3) 28 (63.6) 43 (43.0)
   2 44 (30.6) 9 (20.5) 35 (35.0)
   ≥3 29 (20.1) 7 (15.9) 22 (22.0)
Specific metastasis sites, n (%)
   Brain 22 (15.3) 6 (13.6) 16 (16.0) 0.716
   Liver 10 (6.9) 3 (6.8) 7 (7.0) 1.000
   Bone 57 (39.6) 17 (38.6) 40 (40.0) 0.878
Lines of therapy, n (%) 0.937
   2 76 (52.8) 24 (54.5) 52 (52.0)
   3 49 (34.0) 15 (34.1) 34 (34.0)
   ≥4 19 (13.2) 5 (11.4) 14 (14.0)

a, rare mutations include four L861Q, three G719X, two Ex20ins, two L858R and EX20ins co-mutations, one L858R and S768I co-mutation, one L858R and L861Q co-mutation. TKIs, tyrosine kinase inhibitors; IO, immunotherapy; EGFR, epidermal growth factor receptor; PD-L1, programmed cell death ligand 1.