Improvement of Genetic Testing for Cutaneous Melanoma in Countries With Low to Moderate Incidence
Author(s) -
J. Delaunay,
Ludovic Martin,
Brigitte Bressac–de Paillerets,
Gérard Duru,
Olivier Ingster,
L. Thomas
Publication year - 2017
Publication title -
jama dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.128
H-Index - 166
eISSN - 2168-6084
pISSN - 2168-6068
DOI - 10.1001/jamadermatol.2017.2926
Subject(s) - medicine , cdkn2a , incidence (geometry) , genetic testing , retrospective cohort study , bap1 , melanoma , population , cohort , oncology , cancer , mutation , dermatology , genetics , gene , cancer research , physics , environmental health , optics , biology
Genetic testing for melanoma-prone mutation in France, a country with low to moderate incidence of melanoma, is proposed in cases with 2 invasive cutaneous melanomas and/or related cancers in the same patient, or in first- or second-degree relatives (rule of 2). In preclinical studies, these rules led to disclosure of mutation(s) in more than 10% of these families, the threshold widely accepted to justify genetic testing for cancers.
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