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Activity Number: 211 - Disease Prediction
Type: Contributed
Date/Time: Tuesday, August 10, 2021 : 1:30 PM to 3:20 PM
Sponsor: Section on Statistics in Epidemiology
Abstract #318972
Title: A Bayesian Joint Polyp Profile Model for the Longitudinal Development of Colorectal Cancer (CRC) Precursors That Incorporates a Patient’s Entire History of Colonoscopic Findings
Author(s): Cameron Miller* and Brian Sullivan and Xuejun Qin and Thomas Redding and Jimmy Thomas Efird and Ashton Madison and Kellie Sims and Christina D. Williams and Elizabeth Kobe and David Weiss and David Lieberman and Dawn Provenzale and Elizabeth Hauser
Companies: Cooperative Studies Program Epidemiology Center-Durham and Duke University and Duke University and Cooperative Studies Program Epidemiology Center-Durham and CSPEC/HSR&D/DVAHCS and Cooperative Studies Program Epidemiology Center-Durham and Cooperative Studies Program Epidemiology Center-Durham and Cooperative Studies Program Epidemiology Center-Durham and Cooperative Studies Program Epidemiology Center-Durham and Perry Point VA Medical Center and VA Portland Health Care System and Cooperative Studies Program Epidemiology Center-Durham and Duke University
Keywords: Bayesian modeling; joint modeling; longitudinal disease modeling; colorectal cancer; model development
Abstract:

Accurate risk prediction models for CRC or other relevant neoplastic lesions rely on detailed longitudinal colonoscopic findings. However, to fit seamlessly into available software, polyp-level data are summarized. This results in a potential loss of information and forces investigators to rely on summary covariates. For longitudinal risk prediction models, the summarization choice is particularly challenging. Time is routinely discretized in these models, treating the complex relationship between disease progression and time as simple and distinct. To overcome these limitations, we develop a joint model incorporating a patient’s entire history of colonoscopic findings. We jointly model the longitudinal detection of polyps on colonoscopy and the longitudinal development of advanced adenomas. In the latter outcome we use a continuous time-dependent weighting function to weight contributions of past colonoscopic findings, enabling us to incorporate a patient’s entire colonoscopy record to model the current risk. We test performance of our model using a simulation study and then apply our model to a prospective cohort of asymptomatic Veterans under colonoscopy surveillance.


Authors who are presenting talks have a * after their name.

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