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Journal of Investigative Dermatology
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Journal of Investigative Dermatology
Article . 2016 . Peer-reviewed
License: Elsevier Non-Commercial
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A Model to Predict the Risk of Keratinocyte Carcinomas

Authors: David C. Whiteman; Bridie S. Thompson; Aaron P. Thrift; Maria-Celia Hughes; Chiho Muranushi; Rachel E. Neale; Adele C. Green; +10 Authors

A Model to Predict the Risk of Keratinocyte Carcinomas

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.

Countries
United Kingdom, United Kingdom, Australia
Keywords

Adult, Keratinocytes, Male, 1303 Biochemistry, Dermatology, Biochemistry, 2708 Dermatology, 1307 Cell Biology, Cohort Studies, Age Distribution, Predictive Value of Tests, 1312 Molecular Biology, Journal Article, Odds Ratio, Humans, Prospective Studies, Molecular Biology, Aged, Manchester Cancer Research Centre, Incidence, Biopsy, Needle, Cell Biology, Middle Aged, Prognosis, Immunohistochemistry, ResearchInstitutes_Networks_Beacons/mcrc; name=Manchester Cancer Research Centre, Logistic Models, Area Under Curve, Carcinoma, Squamous Cell, Female, Basal Cell Carcinoma

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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
36
Top 10%
Top 10%
Top 10%
hybrid