Skip to main content
. 2022 Dec 21;13(12):1064. doi: 10.1038/s41419-022-05510-4

Table 2.

Association of demographics and clinicopathological characteristics with BRAF mutation status in Cohort B.

Characteristics Wild type (n = 358) BRAF mutation (n = 59) P
n (%) n (%)
Age (yrs.) 0.31
≤65 237 (66.2) 43 (72.9)
>65 121 (33.8) 16 (27.1)
Gender 0.36
Female 89 (24.9) 18 (30.5)
Male 269 (75.1) 41 (69.5)
Smoking status 0.33
Never smoker 128 (35.8) 25 (42.4)
Former/current smoker 230 (64.2) 34 (57.6)
Stagea 0.33
III 19 (5.3) 5 (8.5)
IV 339 (94.7) 54 (91.5)
ECOG PS 0.25
0–1 331 (92.5) 57 (96.6)
2 27 (7.5) 2 (3.4)
Pathological type 0.16
Adenocarcinoma 315 (88.0) 48 (81.4)
Other types 43 (12.0) 11 (18.6)
Treatment lines 0.01
First line 179 (50.0) 40 (67.8)
Second/later line 179 (50.0) 19 (33.2)
Treatment regimens 0.77
Monotherapy 116 (32.4) 18 (30.5)
Chemotherapy plus ICIs 201 (56.1) 37 (62.7)
Anti-angiogenesis plus ICIs 41 (11.2) 4 (6.8)
PD-L1 expression 0.92b
Negative 33 (9.2) 9 (15.3)
1–49% 46 (12.8) 14 (23.7)
≥50% 31 (8.7) 14 (23.7)
Unkonow 248 (69.3) 22 (37.3)

aUsing the 8th TNM staging classification.

bAnalysis in PD-L1 detected patients.