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. 2022 Mar 10;13:1268. doi: 10.1038/s41467-022-28840-5

Table 1.

Clinical characteristics and prevalence of germline mutations.

Patients With P/LP germline variants Patients without P/LP germline variants Prevalence of P/LP germline variants
Number of patients(N) 106 1688 5.91%
Age at diagnosis—yrs p = 0.28a
 Mean ± SD 58.36 ± 11.51 59.97 ± 11.54
 Median (range) 60.5(29–82) 60(16–94)
 NA(N) 2 77
Gender—N (%) p = 0.56b
 Female 42(39.6) 725(43.0) 5.48%
 Male 64(60.4) 961(57.0) 6.24%
 NA 0 2
Histologic diagnosis—N (%) p = 0.50b
 LUAD 75(70.7) 1148(68.0) 6.13%
 LUSC 10(9.4) 160(9.4) 5.88%
 SCLC 3(2.8) 41(2.4) 6.82%
 Other type 5(4.7) 39(2.3) 11.36%
 NSCLC-NOS 13(12.2) 300(17.7)
Stage at diagnosisc-N (%) p = 0.75b
 I 1 (0.9) 37 (2.2) 2.63%
 II 3 (2.8) 47 (2.8) 6.00%
 III 8 (7.5) 153 (9.1) 4.97%
 IV 76 (71.7) 1034 (61.2) 6.85%
 NA 18(17.0) 417 (24.7)

P/LP pathogenic/likely pathogenic, NA not available, LUAD lung adenocarcinoma, LUSC lung squamous carcinoma, SCLC small cell lung cancer, NOS not otherwise specified; Other histology type included: large cell neuroendocrine carcinoma, adenosquamous carcinoma, sarcomatoid carcinoma, pleomorphic carcinoma, poorly differentiated carcinoma, mucoepidermoid carcinoma, lymphoepithelioid carcinoma, etc.

aP value is calculated with Mann–Whitney test.

bP value is calculated with Chi-square test or Fisher’s exact test.

cThe clinical stage was based on 8th AJCC non-small cell lung cancer stage edition.