A prediction model for colon cancer surveillance data. (6th April 2015)

• Record Type: Journal Article
• Authors: Good, Norm M.; Suresh, Krithika; Young, Graeme P.; Lockett, Trevor J.; Macrae, Finlay A.; Taylor, Jeremy M. G.
• Is Part Of: Statistics in medicine. Volume 34:Number 18(2015)
• Page Start: 2662
• Page End: 2675
• Publication Date: 2015-04-06
• Subjects: Medical statistics -- Periodicals; Statistique médicale -- Périodiques; Statistiques médicales -- Périodiques; 610.727
• DOI: 10.1002/sim.6500
• Languages: English
• ISSNs: 0277-6715

Abstract

<abstract abstract-type="main" id="sim6500-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="sim6500-para-0001">Dynamic prediction models make use of patient‐specific longitudinal data to update individualized survival probability predictions based on current and past information. Colonoscopy (COL) and fecal occult blood test (FOBT) results were collected from two Australian surveillance studies on individuals characterized as high‐risk based on a personal or family history of colorectal cancer. Motivated by a Poisson process, this paper proposes a generalized nonlinear model with a complementary log–log link as a dynamic prediction tool that produces individualized probabilities for the risk of developing advanced adenoma or colorectal cancer (AAC). This model allows predicted risk to depend on a patient's baseline characteristics and time‐dependent covariates. Information on the dates and results of COLs and FOBTs were incorporated using time‐dependent covariates that contributed to patient risk of AAC for a specified period following the test result. These covariates serve to update a person's risk as additional COL, and FOBT test information becomes available. Model selection was conducted systematically through the comparison of Akaike information criterion. Goodness‐of‐fit was assessed with the use of calibration plots to compare the predicted probability of event occurrence with the proportion of events observed. Abnormal COL results were found to significantly increase risk of AAC for 1 year following the test. Positive FOBTs were found to significantly increase the risk of AAC for 3 months following the result. The covariates that incorporated the updated test results were of greater significance and had a larger effect on risk than the baseline variables. Copyright © 2015 John Wiley & Sons, Ltd.</p> </abstract>