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    A model to predict the risk of keratinocyte carcinomas.

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    Authors
    Whiteman, D
    Thompson, B
    Thrift, A
    Hughes, M-C
    Muranushi, C
    Neale, R
    Green, Adèle C
    Olsen, C
    Affiliation
    Population Health Department, QIMR Berghofer Medical Research Institute, 300 Herston Road, Herston, Queensland 4006, Australia
    Issue Date
    2016-02-22
    
    Metadata
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    Abstract
    Basal cell and squamous cell carcinomas of the skin are the commonest cancers in humans, yet no validated tools exist to estimate future risks of developing keratinocyte carcinomas. To develop a prediction tool, we used baseline data from a prospective cohort study (n = 38,726) in Queensland, Australia, and used data linkage to capture all surgically excised keratinocyte carcinomas arising within the cohort. Predictive factors were identified through stepwise logistic regression models. In secondary analyses, we derived separate models within strata of prior skin cancer history, age, and sex. The primary model included terms for 10 items. Factors with the strongest effects were >20 prior skin cancers excised (odds ratio 8.57, 95% confidence interval [95% CI] 6.73-10.91), >50 skin lesions destroyed (odds ratio 3.37, 95% CI 2.85-3.99), age ≥ 70 years (odds ratio 3.47, 95% CI 2.53-4.77), and fair skin color (odds ratio 1.75, 95% CI 1.42-2.15). Discrimination in the validation dataset was high (area under the receiver operator characteristic curve 0.80, 95% CI 0.79-0.81) and the model appeared well calibrated. Among those reporting no prior history of skin cancer, a similar model with 10 factors predicted keratinocyte carcinoma events with reasonable discrimination (area under the receiver operator characteristic curve 0.72, 95% CI 0.70-0.75). Algorithms using self-reported patient data have high accuracy for predicting risks of keratinocyte carcinomas.
    Citation
    A model to predict the risk of keratinocyte carcinomas. 2016: J Invest Dermatol
    Journal
    The Journal of Investigative Dermatology
    URI
    http://hdl.handle.net/10541/604205
    DOI
    10.1016/j.jid.2016.02.008
    PubMed ID
    26908057
    Type
    Article
    Language
    en
    ISSN
    1523-1747
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jid.2016.02.008
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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