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. 2020 Dec 26;2(2):100140. doi: 10.1016/j.jtocrr.2020.100140

Table 3.

Clinical Characteristics of Patients With Nonsquamous NSCLC Who Received ICIs

Characteristics All Patients Responder Nonresponder pa
Total 25 8 (32.0) 17 (68.0)
Age, median, y (range) 63.2 (38.9–85.8) 60.2 (45.5–80.5) 63.9 (38.9–85.8) 0.673b
Sex 1.000
 Female 4 1 (12.5) 3 (17.6)
 Male 21 7 (87.5) 14 (82.4)
Smoking status 1.000
 Nonsmokers 7 2 (25.0) 5 (29.4)
 Smokers 18 6 (75.0) 12 (70.6)
Tumor 0.448
 Adenocarcinoma 22 8 (100.0) 14 (82.4)
 Pleomorphic or sarcomatoid 1 0 (0.0) 1 (5.9)
 NSCLC-NOS 2 0 (0.0) 2 (11.8)
PD-L1 TPS, % 0.225
 >50 12 5 (62.5) 7 (41.2)
 1–49 8 3 (37.5) 5 (29.4)
 <1 5 0 (0.0) 5 (29.4)
Kras mutations 0.030
 G12C 13 7 (87.5) 6 (35.3)
 Non-G12C 12 1 (12.5) 11 (64.7)
 ICIs 0.548
 Pembrolizumab 14 6 (75.0) 8 (47.1)
 Nivolumab 2 0 (0.0) 2 (11.8)
 Atezolizumab 5 1 (12.5) 4 (23.5)
 Otherc 4c 1 (12.5) 3 (17.6)
 Combination therapy 1.000
 Combo 5 2 (25.0) 3 (17.6)
 Single use 20 6 (75.0) 14 (82.4)

Note: Values are given in number (%) unless indicated otherwise.

ICI, immune checkpoint inhibitor; NOS, not otherwise specified; PD-L1, programmed death-ligand 1; TPS, tumor proportion score.

a

By Fisher’s exact test.

b

By Mann-Whitney U test.

c

One tremelimumab plus durvalumab, one tislelizumab (BGB-A317), and two spartalizumab (PDR001).