Table 3.
SPM risk associated with FAS and FASLG polymorphisms after index SCCHN
| No. risk genotypes | Total (No. =1,286) | SPM-free (No. =1,166) | SPM (No. =120) | Pa | HR(95% CI)b | |||
|---|---|---|---|---|---|---|---|---|
| No. | % | No. | % | No. | % | |||
| 0–1 (Ref.c) | 235 | 18.3 | 221 | 19.0 | 14 | 11.7 | 0.103 | 1.00 (Ref) |
| 2 | 480 | 37.3 | 438 | 37.6 | 42 | 35.0 | 1.43 (0.78–2.63) | |
| 3 | 420 | 32.7 | 375 | 32.1 | 45 | 37.5 | 1.83 (1.00–3.36) | |
| 4 | 151 | 11.7 | 132 | 11.3 | 19 | 15.8 | 2.53 (1.26–5.06) | |
| Trend | P=0.004 | |||||||
χ2 test for differences in the distribution of combined genotypes between the patients who developed SPM and the patients who did not.
Adjusted for age, sex, ethnicity, tobacco smoking and alcohol drinking in a Cox model.
Ref. = reference group.