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Interim recruitment prediction for multi-center clinical trials
We introduce a general framework for monitoring, modeling, and predicting the recruitment to multi-center clinical trials. The work is motivated by overly optimistic and narrow prediction intervals produced by existing time-homogeneous recruitment models for multi-center recruitment. We first presen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007446/ https://www.ncbi.nlm.nih.gov/pubmed/32978616 http://dx.doi.org/10.1093/biostatistics/kxaa036 |
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author | Urbas, Szymon Sherlock, Chris Metcalfe, Paul |
author_facet | Urbas, Szymon Sherlock, Chris Metcalfe, Paul |
author_sort | Urbas, Szymon |
collection | PubMed |
description | We introduce a general framework for monitoring, modeling, and predicting the recruitment to multi-center clinical trials. The work is motivated by overly optimistic and narrow prediction intervals produced by existing time-homogeneous recruitment models for multi-center recruitment. We first present two tests for detection of decay in recruitment rates, together with a power study. We then introduce a model based on the inhomogeneous Poisson process with monotonically decaying intensity, motivated by recruitment trends observed in oncology trials. The general form of the model permits adaptation to any parametric curve-shape. A general method for constructing sensible parameter priors is provided and Bayesian model averaging is used for making predictions which account for the uncertainty in both the parameters and the model. The validity of the method and its robustness to misspecification are tested using simulated datasets. The new methodology is then applied to oncology trial data, where we make interim accrual predictions, comparing them to those obtained by existing methods, and indicate where unexpected changes in the accrual pattern occur. |
format | Online Article Text |
id | pubmed-9007446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90074462022-04-14 Interim recruitment prediction for multi-center clinical trials Urbas, Szymon Sherlock, Chris Metcalfe, Paul Biostatistics Articles We introduce a general framework for monitoring, modeling, and predicting the recruitment to multi-center clinical trials. The work is motivated by overly optimistic and narrow prediction intervals produced by existing time-homogeneous recruitment models for multi-center recruitment. We first present two tests for detection of decay in recruitment rates, together with a power study. We then introduce a model based on the inhomogeneous Poisson process with monotonically decaying intensity, motivated by recruitment trends observed in oncology trials. The general form of the model permits adaptation to any parametric curve-shape. A general method for constructing sensible parameter priors is provided and Bayesian model averaging is used for making predictions which account for the uncertainty in both the parameters and the model. The validity of the method and its robustness to misspecification are tested using simulated datasets. The new methodology is then applied to oncology trial data, where we make interim accrual predictions, comparing them to those obtained by existing methods, and indicate where unexpected changes in the accrual pattern occur. Oxford University Press 2020-09-25 /pmc/articles/PMC9007446/ /pubmed/32978616 http://dx.doi.org/10.1093/biostatistics/kxaa036 Text en © The Author 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Urbas, Szymon Sherlock, Chris Metcalfe, Paul Interim recruitment prediction for multi-center clinical trials |
title | Interim recruitment prediction for multi-center clinical trials |
title_full | Interim recruitment prediction for multi-center clinical trials |
title_fullStr | Interim recruitment prediction for multi-center clinical trials |
title_full_unstemmed | Interim recruitment prediction for multi-center clinical trials |
title_short | Interim recruitment prediction for multi-center clinical trials |
title_sort | interim recruitment prediction for multi-center clinical trials |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007446/ https://www.ncbi.nlm.nih.gov/pubmed/32978616 http://dx.doi.org/10.1093/biostatistics/kxaa036 |
work_keys_str_mv | AT urbasszymon interimrecruitmentpredictionformulticenterclinicaltrials AT sherlockchris interimrecruitmentpredictionformulticenterclinicaltrials AT metcalfepaul interimrecruitmentpredictionformulticenterclinicaltrials |