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Estimating treatment effects for individual patients based on the results of randomised clinical trials
Objectives To predict treatment effects for individual patients based on data from randomised trials, taking rosuvastatin treatment in the primary prevention of cardiovascular disease as an example, and to evaluate the net benefit of making treatment decisions for individual patients based on a pred...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184644/ https://www.ncbi.nlm.nih.gov/pubmed/21968126 http://dx.doi.org/10.1136/bmj.d5888 |
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author | Dorresteijn, Johannes A N Visseren, Frank L J Ridker, Paul M Wassink, Annemarie M J Paynter, Nina P Steyerberg, Ewout W van der Graaf, Yolanda Cook, Nancy R |
author_facet | Dorresteijn, Johannes A N Visseren, Frank L J Ridker, Paul M Wassink, Annemarie M J Paynter, Nina P Steyerberg, Ewout W van der Graaf, Yolanda Cook, Nancy R |
author_sort | Dorresteijn, Johannes A N |
collection | PubMed |
description | Objectives To predict treatment effects for individual patients based on data from randomised trials, taking rosuvastatin treatment in the primary prevention of cardiovascular disease as an example, and to evaluate the net benefit of making treatment decisions for individual patients based on a predicted absolute treatment effect. Setting As an example, data were used from the Justification for the Use of Statins in Prevention (JUPITER) trial, a randomised controlled trial evaluating the effect of rosuvastatin 20 mg daily versus placebo on the occurrence of cardiovascular events (myocardial infarction, stroke, arterial revascularisation, admission to hospital for unstable angina, or death from cardiovascular causes). Population 17 802 healthy men and women who had low density lipoprotein cholesterol levels of less than 3.4 mmol/L and high sensitivity C reactive protein levels of 2.0 mg/L or more. Methods Data from the Justification for the Use of Statins in Prevention trial were used to predict rosuvastatin treatment effect for individual patients based on existing risk scores (Framingham and Reynolds) and on a newly developed prediction model. We compared the net benefit of prediction based rosuvastatin treatment (selective treatment of patients whose predicted treatment effect exceeds a decision threshold) with the net benefit of treating either everyone or no one. Results The median predicted 10 year absolute risk reduction for cardiovascular events was 4.4% (interquartile range 2.6-7.0%) based on the Framingham risk score, 4.2% (2.5-7.1%) based on the Reynolds score, and 3.9% (2.5-6.1%) based on the newly developed model (optimal fit model). Prediction based treatment was associated with more net benefit than treating everyone or no one, provided that the decision threshold was between 2% and 7%, and thus that the number willing to treat (NWT) to prevent one cardiovascular event over 10 years was between 15 and 50. Conclusions Data from randomised trials can be used to predict treatment effect in terms of absolute risk reduction for individual patients, based on a newly developed model or, if available, existing risk scores. The value of such prediction of treatment effect for medical decision making is conditional on the NWT to prevent one outcome event. Trial registration number Clinicaltrials.gov NCT00239681. |
format | Online Article Text |
id | pubmed-3184644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-31846442011-10-13 Estimating treatment effects for individual patients based on the results of randomised clinical trials Dorresteijn, Johannes A N Visseren, Frank L J Ridker, Paul M Wassink, Annemarie M J Paynter, Nina P Steyerberg, Ewout W van der Graaf, Yolanda Cook, Nancy R BMJ Research Objectives To predict treatment effects for individual patients based on data from randomised trials, taking rosuvastatin treatment in the primary prevention of cardiovascular disease as an example, and to evaluate the net benefit of making treatment decisions for individual patients based on a predicted absolute treatment effect. Setting As an example, data were used from the Justification for the Use of Statins in Prevention (JUPITER) trial, a randomised controlled trial evaluating the effect of rosuvastatin 20 mg daily versus placebo on the occurrence of cardiovascular events (myocardial infarction, stroke, arterial revascularisation, admission to hospital for unstable angina, or death from cardiovascular causes). Population 17 802 healthy men and women who had low density lipoprotein cholesterol levels of less than 3.4 mmol/L and high sensitivity C reactive protein levels of 2.0 mg/L or more. Methods Data from the Justification for the Use of Statins in Prevention trial were used to predict rosuvastatin treatment effect for individual patients based on existing risk scores (Framingham and Reynolds) and on a newly developed prediction model. We compared the net benefit of prediction based rosuvastatin treatment (selective treatment of patients whose predicted treatment effect exceeds a decision threshold) with the net benefit of treating either everyone or no one. Results The median predicted 10 year absolute risk reduction for cardiovascular events was 4.4% (interquartile range 2.6-7.0%) based on the Framingham risk score, 4.2% (2.5-7.1%) based on the Reynolds score, and 3.9% (2.5-6.1%) based on the newly developed model (optimal fit model). Prediction based treatment was associated with more net benefit than treating everyone or no one, provided that the decision threshold was between 2% and 7%, and thus that the number willing to treat (NWT) to prevent one cardiovascular event over 10 years was between 15 and 50. Conclusions Data from randomised trials can be used to predict treatment effect in terms of absolute risk reduction for individual patients, based on a newly developed model or, if available, existing risk scores. The value of such prediction of treatment effect for medical decision making is conditional on the NWT to prevent one outcome event. Trial registration number Clinicaltrials.gov NCT00239681. BMJ Publishing Group Ltd. 2011-10-03 /pmc/articles/PMC3184644/ /pubmed/21968126 http://dx.doi.org/10.1136/bmj.d5888 Text en © Dorresteijn et al 2011 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Research Dorresteijn, Johannes A N Visseren, Frank L J Ridker, Paul M Wassink, Annemarie M J Paynter, Nina P Steyerberg, Ewout W van der Graaf, Yolanda Cook, Nancy R Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title | Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title_full | Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title_fullStr | Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title_full_unstemmed | Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title_short | Estimating treatment effects for individual patients based on the results of randomised clinical trials |
title_sort | estimating treatment effects for individual patients based on the results of randomised clinical trials |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184644/ https://www.ncbi.nlm.nih.gov/pubmed/21968126 http://dx.doi.org/10.1136/bmj.d5888 |
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