Skip to main content
. Author manuscript; available in PMC: 2022 Feb 15.
Published in final edited form as: Clin Cancer Res. 2021 Jun 11;27(16):4587–4598. doi: 10.1158/1078-0432.CCR-21-0180

Table 2.

Clinical characteristics associated with class of RAS mutation.

RAS/BRAF Wild-type
N=1069
KRAS Mutant
N=1226
NRAS Mutant
N=127
BRAF V600 Mutant
N=168
P RAS/BRAF Wild-type
N=1069
Exon 2 KRAS Mutation
N=1033
Extended RAS Mutation
N=292
Atypical RAS Mutation
N=21
P
Characteristic
Median Age (IQR) 54 (45–62) 55 (45–63) 57 (47–65) 60 (54–67) <0.0001 54 (45–62) 55 (45–63) 57 (47–65) 55 (45–67) 0.018
Sex
 Female 394 (37%) 593 (48%) 65 (51%) 93 (55%) <0.0001 394 (37%) 505 (49%) 137 (47%) 11 (52%) <0.0001
 Male 675 (63%) 633 (52%) 62 (49%) 75 (45%) 675 (63%) 528 (51%) 155 (53%) 10 (48%)
Location*
 Right 216 (20%) 477 (39%) 40 (31%) 116 (70%) <0.0001 216 (20%) 399 (39%) 104 (36%) 10 (48%) <0.0001
 Left 849 (80%) 742 (61%) 87 (69%) 50 (30%) 849 (80%) 631 (61%) 184 (64%) 11 (52%)
MSI Status*
 MSS 766 (96%) 870 (96%) 99 (99%) 99 (83%) <0.0001 766 (96%) 735 (97%) 218 (96%) 13 (87%) 0.25
 MSI-H 30 (4%) 35 (4%) 1 (1%) 20 (17%) 30 (4%) 26 (3%) 8 (4%) 2 (13%)
 Unknown 273 321 27 49 273 272 66 6
*

Percent represent the proportion of patients with a known result for that variable.

Total n=2581 patients, however patients with multiple variants may be included in multiple categories for comparisons between KRAS, NRAS, and BRAF V600 but not RAS mutation class. All RAS mutation categories (atypical, extended, and KRAS exon 2) are grouped together by gene on the left half of the table.

IQR=interquartile range