TY - JOUR
T1 - Independent validation of six melanoma risk prediction models.
AU - Olsen, Catherine M
AU - Neale, Rachel E
AU - Green, Adèle C
AU - Webb, Penelope M
AU - Whiteman, David C
PY - 2014/12/30
Y1 - 2014/12/30
N2 - Identifying people at high risk of melanoma is important for targeted prevention activities and surveillance. Several tools have been developed to classify melanoma risk, but few have been independently validated. We assessed the discriminatory performance of six melanoma prediction tools by applying them to individuals from two independent datasets, one comprising 762 melanoma cases and the second a population-based sample of 42,116 people without melanoma. We compared the model predictions with actual melanoma status to measure sensitivity and specificity. The performance of the models was variable with sensitivity ranging from 97.7 to 10.5% and specificity from 99.6 to 1.3%. The ability of all the models to discriminate between cases and controls, however, was generally high. The model developed by MacKie and colleagues (1989) had higher sensitivity and specificity for men (0.89 and 0.88) than women (0.79 and 0.72). The tool developed by Cho and colleagues (2005) was highly specific (men, 0.92; women, 0.99) but considerably less sensitive (men, 0.64; women, 0.37). Other models were either highly specific but lacked sensitivity or had low to very low specificity and higher sensitivity. Poor performance was partly attributable to use of non-standardised assessment items, and various differing interpretations of what constitutes 'high risk'.Journal of Investigative Dermatology accepted article preview online, 30 December 2014. doi:10.1038/jid.2014.533.
AB - Identifying people at high risk of melanoma is important for targeted prevention activities and surveillance. Several tools have been developed to classify melanoma risk, but few have been independently validated. We assessed the discriminatory performance of six melanoma prediction tools by applying them to individuals from two independent datasets, one comprising 762 melanoma cases and the second a population-based sample of 42,116 people without melanoma. We compared the model predictions with actual melanoma status to measure sensitivity and specificity. The performance of the models was variable with sensitivity ranging from 97.7 to 10.5% and specificity from 99.6 to 1.3%. The ability of all the models to discriminate between cases and controls, however, was generally high. The model developed by MacKie and colleagues (1989) had higher sensitivity and specificity for men (0.89 and 0.88) than women (0.79 and 0.72). The tool developed by Cho and colleagues (2005) was highly specific (men, 0.92; women, 0.99) but considerably less sensitive (men, 0.64; women, 0.37). Other models were either highly specific but lacked sensitivity or had low to very low specificity and higher sensitivity. Poor performance was partly attributable to use of non-standardised assessment items, and various differing interpretations of what constitutes 'high risk'.Journal of Investigative Dermatology accepted article preview online, 30 December 2014. doi:10.1038/jid.2014.533.
U2 - 10.1038/jid.2014.533
DO - 10.1038/jid.2014.533
M3 - Article
C2 - 25548858
SN - 1523-1747
JO - The Journal of investigative dermatology
JF - The Journal of investigative dermatology
ER -