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. Author manuscript; available in PMC: 2010 Apr 15.
Published in final edited form as: Cancer Res. 2009 Apr 7;69(8):3681–3688. doi: 10.1158/0008-5472.CAN-09-0015

Table 5.

Frequency distribution of the number of patients with none or at least one sequencing mutation in KRAS, SMAD4, CDKN2A/P16 or TP53. (NS= non-smoker, S= smoker)

Discovery Screen Validation Screen Combined Samples

Non-smokers Smokers P Non-smokers Smokers P Non-smokers Smokers P



N % N % N % N % N % N %
KRAS
Wild-type 0 (0) 0 (0) - 0 (0) 1 (2) - 0 (0) 1 (2) 1.00
Mutated 13 (100) 11 (100) 37 (100) 52 (98) 50 (100) 63 (98)
SMAD4
Wild-type 8 (62) 8 (73) 0.68 28 (76) 39 (74) 1.00 36 (72) 47 (73) 1.00
Mutated 5 (38) 3 (27) 9 (24) 14 (26) 14 (28) 17 (27)
CDKN2A/p16
Wild-type 12 (92) 10 (91) 1.00 30 (81) 38 (72) 0.33 42 (84) 48 (75) 0.26
Mutated 1 (8) 1 (9) 7 (19) 15 (28) 8 (16) 16 (25)
TP53
Wild-type 2 (15) 4 (36) 0.36 4 (11) 10 (19) 0.38 6 (12) 14 (22) 0.22
Mutated 11 (85) 7 (64) 33 (89) 43 (81) 44 (88) 50 (78)