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AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials

In phase I cancer clinical trials, the maximum tolerated dose of a new drug is often found by a dose-escalation method known as the A + B design. We have developed an interactive web application, AplusB, which computes and returns exact operating characteristics of A + B trial designs. The applicati...

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Detalles Bibliográficos
Autores principales: Wheeler, Graham M., Sweeting, Michael J., Mander, Adrian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942070/
https://www.ncbi.nlm.nih.gov/pubmed/27403961
http://dx.doi.org/10.1371/journal.pone.0159026
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author Wheeler, Graham M.
Sweeting, Michael J.
Mander, Adrian P.
author_facet Wheeler, Graham M.
Sweeting, Michael J.
Mander, Adrian P.
author_sort Wheeler, Graham M.
collection PubMed
description In phase I cancer clinical trials, the maximum tolerated dose of a new drug is often found by a dose-escalation method known as the A + B design. We have developed an interactive web application, AplusB, which computes and returns exact operating characteristics of A + B trial designs. The application has a graphical user interface (GUI), requires no programming knowledge and is free to access and use on any device that can open an internet browser. A customised report is available for download for each design that contains tabulated operating characteristics and informative plots, which can then be compared with other dose-escalation methods. We present a step-by-step guide on how to use this application and provide several illustrative examples of its capabilities.
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spelling pubmed-49420702016-08-01 AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials Wheeler, Graham M. Sweeting, Michael J. Mander, Adrian P. PLoS One Research Article In phase I cancer clinical trials, the maximum tolerated dose of a new drug is often found by a dose-escalation method known as the A + B design. We have developed an interactive web application, AplusB, which computes and returns exact operating characteristics of A + B trial designs. The application has a graphical user interface (GUI), requires no programming knowledge and is free to access and use on any device that can open an internet browser. A customised report is available for download for each design that contains tabulated operating characteristics and informative plots, which can then be compared with other dose-escalation methods. We present a step-by-step guide on how to use this application and provide several illustrative examples of its capabilities. Public Library of Science 2016-07-12 /pmc/articles/PMC4942070/ /pubmed/27403961 http://dx.doi.org/10.1371/journal.pone.0159026 Text en © 2016 Wheeler et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wheeler, Graham M.
Sweeting, Michael J.
Mander, Adrian P.
AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title_full AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title_fullStr AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title_full_unstemmed AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title_short AplusB: A Web Application for Investigating A + B Designs for Phase I Cancer Clinical Trials
title_sort aplusb: a web application for investigating a + b designs for phase i cancer clinical trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942070/
https://www.ncbi.nlm.nih.gov/pubmed/27403961
http://dx.doi.org/10.1371/journal.pone.0159026
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