Published Estimates of Cancer Risk for p16 Mutation Carriers
| Site |
Population Risk1 |
Hereditary Risk |
| Melanoma |
Risk of
primary melanoma:
<1% by age 50
~1% by age 80 |
Risk of primary melanoma:
50% by age 502
76% by age 802 Risk of second melanomas:
Increased risk for second melanomas in p16 mutation carriers previously
diagnosed with one melanoma3,4
15% of patients with multiple primary melanomas (MPM) will have a mutation
in the p16 gene4 |
| Pancreatic |
<1% by age 75 |
Up to 17% by age 75 in some families5 |
- Ries LAG, Eisner MP, Kosary CL, Hankley BF, Miller BA, Clegg L, Edwards BK (eds). SEER Cancer Statistics Review, 1973-1999, National Cancer Institute. Bethesda, MD, http://seer.cancer.gov/csr/1973_1999/. Accessed December 30, 2002.
- Bishop DT, Demenais F, Goldstein AM, et al. Geographical variation in the penetrance of CDKN2A mutations for melanoma. J Natl Cancer Inst. 2002;94:894-903.
- Hashemi J, Platz A, Ueno T, Stierner U, Ringborg U, Hannson J. CDKN2A germline mutations in individuals with multiple cutaneous melanomas. Cancer Res. 2000;60:6864-6867.
- Monzon J, Liu L, Brill H, et al. CDKN2A mutations in multiple primary melanomas. N Engl J Med. 1998;338:879-887.
- Vasen HF, Gruis NA, Frants RR, van Der Velden PA, Hille ET, Bergman W. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden). Int J Cancer. 2000;87:809-811.
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A genetic test for hereditary melanoma
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