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Table 5 Cross-tabulation of mutation prevalence and odds ratios, according to family history and multiple primaries

From: Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom

 

No family history

One affected relative

Two or more affected relatives

Prevalence of CDKN2A pathogenic mutation

   

One primary only

1.1% (27/2495)

3.8% (7/185)

20.0% (8/40)

Two primaries

3.6% (5/140)

14.3% (3/21)

33.3% (2/6)

Three or more primaries

26.7% (8/30)

20.0% (1/5)

60.0% (3/5)

Odds ratios 1 and 95% confidence intervals

   

One primary only

1 (reference)

3.3 (1.4, 7.7)

18.9 (7.8, 45.5)

Two primaries

3.5 (1.3, 9.3)

13.1 (3.6, 47.8)

42.7 (7.5, 244.0)

Three or more primaries

33.1 (13.5, 81.5)

23.8 (2.6, 221.2)

146.6 (23.1, 928.1)

  1. 1Multivariate ORs adjusted for age at diagnosis and country.