QUALITATIVE AND OUTCOMES RESEARCH
Article first published online: 20 Jul 2017
Receiving information about genomic risk of melanoma might trigger conversations about skin cancer prevention and skin examinations.
To explore conversations prompted by receiving personalized genomic risk of melanoma with family, friends and health professionals.
We used a mixed‐methods approach. Participants without a personal history and unselected for a family history of melanoma (n = 103, aged 21–69 years, 53% women) completed questionnaires 3 months after receiving a personalized melanoma genomic risk assessment. Semistructured interviews were undertaken with 30 participants in high, average and low genomic risk categories, and data were analysed thematically.
From the questionnaires, 74% of participants communicated their genomic risk information with family, and 49% with friends. Communication with a health professional differed by risk level: 41%, 16% and 12% for high, average and low risk, respectively (P = 0·01). Qualitative analysis showed that perceived ‘shared risk’ and perceived interest of family and friends were motivations for discussing risk or prevention behaviours. The information prompted conversations with family and health professionals about sun protection and skin checks, and general conversations about melanoma risk with friends. Reasons for not discussing with family included existing personal or family health concerns, or existing high levels of sun protection behaviour among family members.
Personalized melanoma genomic risk information can prompt risk‐appropriate discussions about skin cancer prevention and skin examinations with family and health professionals. Sharing this information with others might increase its impact on melanoma prevention and skin examination behaviours, and this process could be used to encourage healthy behaviour change within families.
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