A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.

When some individuals are screen-detected before the beginning of the study, but otherwise would have been diagnosed symptomatically during the study, this results in different case-ascertainment probabilities among screened and unscreened participants, referred to here as lead-time-biased case-asce...

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Main Authors: Rick J Jansen, Bruce H Alexander, Richard B Hayes, Anthony B Miller, Sholom Wacholder, Timothy R Church
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5858824?pdf=render
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author Rick J Jansen
Bruce H Alexander
Richard B Hayes
Anthony B Miller
Sholom Wacholder
Timothy R Church
author_facet Rick J Jansen
Bruce H Alexander
Richard B Hayes
Anthony B Miller
Sholom Wacholder
Timothy R Church
author_sort Rick J Jansen
collection DOAJ
description When some individuals are screen-detected before the beginning of the study, but otherwise would have been diagnosed symptomatically during the study, this results in different case-ascertainment probabilities among screened and unscreened participants, referred to here as lead-time-biased case-ascertainment (LTBCA). In fact, this issue can arise even in risk-factor studies nested within a randomized screening trial; even though the screening intervention is randomly allocated to trial arms, there is no randomization to potential risk-factors and uptake of screening can differ by risk-factor strata. Under the assumptions that neither screening nor the risk factor affects underlying incidence and no other forms of bias operate, we simulate and compare the underlying cumulative incidence and that observed in the study due to LTBCA. The example used will be constructed from the randomized Prostate, Lung, Colorectal, and Ovarian cancer screening trial. The derived mathematical model is applied to simulating two nested studies to evaluate the potential for screening bias in observational lung cancer studies. Because of differential screening under plausible assumptions about preclinical incidence and duration, the simulations presented here show that LTBCA due to chest x-ray screening can significantly increase the estimated risk of lung cancer due to smoking by 1% and 50%. Traditional adjustment methods cannot account for this bias, as the influence screening has on observational study estimates involves events outside of the study observation window (enrollment and follow-up) that change eligibility for potential participants, thus biasing case ascertainment.
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spelling doaj.art-e28108994205483a9d2aff5d9d81551f2022-12-22T03:37:01ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019460810.1371/journal.pone.0194608A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.Rick J JansenBruce H AlexanderRichard B HayesAnthony B MillerSholom WacholderTimothy R ChurchWhen some individuals are screen-detected before the beginning of the study, but otherwise would have been diagnosed symptomatically during the study, this results in different case-ascertainment probabilities among screened and unscreened participants, referred to here as lead-time-biased case-ascertainment (LTBCA). In fact, this issue can arise even in risk-factor studies nested within a randomized screening trial; even though the screening intervention is randomly allocated to trial arms, there is no randomization to potential risk-factors and uptake of screening can differ by risk-factor strata. Under the assumptions that neither screening nor the risk factor affects underlying incidence and no other forms of bias operate, we simulate and compare the underlying cumulative incidence and that observed in the study due to LTBCA. The example used will be constructed from the randomized Prostate, Lung, Colorectal, and Ovarian cancer screening trial. The derived mathematical model is applied to simulating two nested studies to evaluate the potential for screening bias in observational lung cancer studies. Because of differential screening under plausible assumptions about preclinical incidence and duration, the simulations presented here show that LTBCA due to chest x-ray screening can significantly increase the estimated risk of lung cancer due to smoking by 1% and 50%. Traditional adjustment methods cannot account for this bias, as the influence screening has on observational study estimates involves events outside of the study observation window (enrollment and follow-up) that change eligibility for potential participants, thus biasing case ascertainment.http://europepmc.org/articles/PMC5858824?pdf=render
spellingShingle Rick J Jansen
Bruce H Alexander
Richard B Hayes
Anthony B Miller
Sholom Wacholder
Timothy R Church
A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
PLoS ONE
title A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
title_full A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
title_fullStr A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
title_full_unstemmed A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
title_short A mathematical model of case-ascertainment bias: Applied to case-control studies nested within a randomized screening trial.
title_sort mathematical model of case ascertainment bias applied to case control studies nested within a randomized screening trial
url http://europepmc.org/articles/PMC5858824?pdf=render
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