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. 2022 Sep 9;13:975246. doi: 10.3389/fimmu.2022.975246

Table 1.

Characteristics of patients with sensitive EGFR mutations receiving ICIs.

Characteristic All patients (N = 99)
Median age (range), y 59(34-92)
Gender, n (%)
 Male 44 (44.44)
 Female 55 (55.56)
ECOG score, n (%)
 0-1 70 (70.71)
 ≥2 29 (29.29)
Smoking history, n (%)
 Current or former 22 (22.22)
 Never 77 (77.78)
Pathologic type, n (%)
 Adenocarcinoma 90 (90.91)
 Squamous cell carcinoma 3 (3.03)
 Mixed type 6 (6.06)
TNM stage, n (%)
 IIIc 3 (3.03)
 IV 96 (96.97)
Sites of metastasis
 Brain 41 (41.41)
 Liver 21 (21.21)
 Bone 54 (54.55)
Primary EGFR mutation
 19del 50 (50.51)
 L858R 42 (42.42)
 others 7 (7.07)
Secondary T790M mutation
 Yes 28 (28.28)
 No 37 (37.37)
 Unknown 34 (34.34)
Previous EGFR-TKI treatment
 1st/2nd generation TKI 44 (44.44)
 1st/2nd ➝3rd generation TKI 48 (48.48)
 3rd generation TKI 7 (7.07)
Prior lines of therapy, n (%)
 ≤2 43 (43.43)
 >2 56 (56.57)
ICIs
 Anti-PD-1 antibody 93 (93.94)
 Anti-PD-L1 antibody 6 (6.06)
Treatment
 Monotherapy 20 (20.20)
 Combination therapy
 I+C 27 (27.27)
 I+A 19 (19.19)
 I+A+C 28 (28.28)
 PD-1 inhibitor + CTLA-4 inhibitor 1 (1.01)
 PD-1 inhibitor + EGFR-TKI 4 (4.04)

ECOG, Eastern Cooperative Oncology Group; EGFR, epidermal growth factor receptor; 19del, exon 19 deletion; ICI, immune checkpoint inhibitor; PD-1, programmed death 1; PD-L1, programmed cell death-ligand 1; I + C, Immunotherapy-chemotherapy combination treatment; I + A, Immunotherapy-antiangiogenic combination treatment; I + A + C, Immunotherapy-antiangiogenic-chemotherapy combination treatment; CTLA-4, cytotoxic T-cell lymphocyte-4; TKI, tyrosine kinase inhibitor.