Journal article
Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?
AK Smit, LA Keogh, AJ Newson, PN Butow, K Dunlop, RL Morton, J Kirk, D Espinoza, AE Cust
British Journal of Dermatology | OXFORD UNIV PRESS | Published : 2017
DOI: 10.1111/bjd.15744
Abstract
Background: Receiving information about genomic risk of melanoma might trigger conversations about skin cancer prevention and skin examinations. Objectives: To explore conversations prompted by receiving personalized genomic risk of melanoma with family, friends and health professionals. Methods: 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 themat..
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Awarded by Sydney West Translational Cancer Research Centre
Funding Acknowledgements
This study received funding from the Sydney Catalyst Translational Cancer Research Centre and The University of Sydney Cancer Strategic Priority Area for Research Collaboration (SPARC) Implementation Scheme. A.E.C. received Career Development Fellowships from the National Health and Medical Research Council of Australia (NHMRC; 1063593) and Cancer Institute NSW (15/CDF/1-14). R.L.M. was supported by an NHMRC Sidney Sax Fellowship (1054216). P.N.B. was supported by an NHMRC Fellowship (1022582).