Cargando…

How many strata in an RCT? A flexible approach

BACKGROUND: The need to allow for prognostic factors when designing and analysing cancer trials is well recognised, but the possibility of overstratification should be avoided by restricting the number of strata. The proposed method improves on existing guidance by being based on explicit principles...

Descripción completa

Detalles Bibliográficos
Autor principal: Silcocks, P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314793/
https://www.ncbi.nlm.nih.gov/pubmed/22415237
http://dx.doi.org/10.1038/bjc.2012.84
_version_ 1782228140231229440
author Silcocks, P
author_facet Silcocks, P
author_sort Silcocks, P
collection PubMed
description BACKGROUND: The need to allow for prognostic factors when designing and analysing cancer trials is well recognised, but the possibility of overstratification should be avoided by restricting the number of strata. The proposed method improves on existing guidance by being based on explicit principles and being more adaptable to circumstances, and should be of particular use to clinicians when designing a trial. METHODS: Given a proposed sample size, a minimum allowable number in a stratum and an acceptable risk of observing fewer than this minimum, the number of strata can then be obtained by assuming a Poisson distribution for the number of observations per stratum. This can easily be programmed into Excel. RESULTS: An example is given for a hypothetical typical trial of 250 patients, which for 80% power and 5% two-sided significance would correspond to a Cohen's effect size of 0.355 (about halfway between the ‘small’ and ‘moderate’ thresholds). To have a <1% risk of fewer than 10 patients in a stratum, no >13 strata should be considered. For a survival analysis with the same overall sample size but 170 deaths, no >9 strata would be prudent. In the context of a cancer trial this could easily be met by only two prognostic variables. CONCLUSION: The method proposed is flexible and based on explicit principles and may be applied in the design or analysis of both clinical trials and epidemiological studies.
format Online
Article
Text
id pubmed-3314793
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-33147932013-03-27 How many strata in an RCT? A flexible approach Silcocks, P Br J Cancer Short Communication BACKGROUND: The need to allow for prognostic factors when designing and analysing cancer trials is well recognised, but the possibility of overstratification should be avoided by restricting the number of strata. The proposed method improves on existing guidance by being based on explicit principles and being more adaptable to circumstances, and should be of particular use to clinicians when designing a trial. METHODS: Given a proposed sample size, a minimum allowable number in a stratum and an acceptable risk of observing fewer than this minimum, the number of strata can then be obtained by assuming a Poisson distribution for the number of observations per stratum. This can easily be programmed into Excel. RESULTS: An example is given for a hypothetical typical trial of 250 patients, which for 80% power and 5% two-sided significance would correspond to a Cohen's effect size of 0.355 (about halfway between the ‘small’ and ‘moderate’ thresholds). To have a <1% risk of fewer than 10 patients in a stratum, no >13 strata should be considered. For a survival analysis with the same overall sample size but 170 deaths, no >9 strata would be prudent. In the context of a cancer trial this could easily be met by only two prognostic variables. CONCLUSION: The method proposed is flexible and based on explicit principles and may be applied in the design or analysis of both clinical trials and epidemiological studies. Nature Publishing Group 2012-03-27 2012-03-13 /pmc/articles/PMC3314793/ /pubmed/22415237 http://dx.doi.org/10.1038/bjc.2012.84 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Short Communication
Silcocks, P
How many strata in an RCT? A flexible approach
title How many strata in an RCT? A flexible approach
title_full How many strata in an RCT? A flexible approach
title_fullStr How many strata in an RCT? A flexible approach
title_full_unstemmed How many strata in an RCT? A flexible approach
title_short How many strata in an RCT? A flexible approach
title_sort how many strata in an rct? a flexible approach
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314793/
https://www.ncbi.nlm.nih.gov/pubmed/22415237
http://dx.doi.org/10.1038/bjc.2012.84
work_keys_str_mv AT silcocksp howmanystratainanrctaflexibleapproach