2008
DOI: 10.1038/sj.bjc.6604489
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Modification of second cancer risk after malignant melanoma by parental history of cancer

Abstract: The Swedish Family-Cancer Database was used to quantify the incidence of second tumours in melanoma patients with a parental history of cancer. Patients with parents affected by melanoma showed a 32.3-fold risk of second primary melanomas, which was greater than a multiplicative interaction.

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Cited by 11 publications
(14 citation statements)
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“…Young age at onset of the initial cancer may be an indication of a genetic predisposition [ 61 ]. Contrary to previously reported work [ 21 , 62 , 63 ], having a parent with cancer did not generally increase the risk of being diagnosed with a subsequent malignancy. However, analyses restricted to individuals born after 1950, showed a near 50% increase in risk when either parent had a history of cancer.…”
Section: Discussioncontrasting
confidence: 99%
“…Young age at onset of the initial cancer may be an indication of a genetic predisposition [ 61 ]. Contrary to previously reported work [ 21 , 62 , 63 ], having a parent with cancer did not generally increase the risk of being diagnosed with a subsequent malignancy. However, analyses restricted to individuals born after 1950, showed a near 50% increase in risk when either parent had a history of cancer.…”
Section: Discussioncontrasting
confidence: 99%
“…Among the few populationbased studies assessing the risk of second melanoma, 3,8,9 this study additionally assessed the risk of next melanoma by the number of previous melanomas, stratified by familial and sporadic cases separately, and by sex, age at diagnosis, anatomical subsite, and histologic subtype of the first melanoma. To our knowledge, the risk of next melanoma in patients with 2 or more previous melanomas stratified by familial and sporadic cases separately has not yet been reported.…”
Section: Discussionmentioning
confidence: 99%
“…All cancer-related deaths were stratified into MM, SPC, and other causes, including cancers defined in death certificates and non-neoplastic causes of death. Additive and multiplicative interactions of family history and risk of SPC were tested as described 11 .…”
Section: Methodsmentioning
confidence: 99%