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. Author manuscript; available in PMC: 2013 Jan 15.
Published in final edited form as: Cancer. 2011 Jun 29;118(2):485–492. doi: 10.1002/cncr.26222

Table 2. SPM risk associated with p53 and p73 polymorphisms after index SCCHN.

Genotypes and no. of variant alleles Total
(No. = 1269)
SPM/Total SPM-free
(No. = 1160)
SPM
(No. = 109)
Pa HR(95% CI)b

No. % % No. % No. %
p53 0.008
WW 655 51.6 6.6 612 52.8 43 39.4 1.00 (Reference)
WP+PP 614 48.4 10.7 548 47.2 66 60.6 1.58 (1.07-2.34)
p73 0.019
GA+ AA 530 41.8 6.4 496 42.8 34 31.2 1.00 (Reference)
GG 739 58.2 10.1 664 57.2 75 68.8 1.68 (1.12-2.52)
Combined risk genotypes 0.002
Low risk group 279 22.0 4.7 266 22.9 13 11.9 1.00 (Reference)
Medium risk group 627 49.4 8.1 576 49.7 51 46.8 1.66 (1.00-3.06)
High risk group 363 28.6 12.4 318 27.4 45 41.3 2.69 (1.44-5.00)
Trend test 0.0007
a

χ2 test for differences in the distribution of p73 genotypes between the patients who developed SPM and the patients who did not.

b

Adjusted for age, sex, ethnicity, tobacco smoking and alcohol drinking in a Cox model.