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Revisiting the relationship between baseline risk and risk under treatment

BACKGROUND: In medical practice, it is generally accepted that the 'effect model' describing the relationship between baseline risk and risk under treatment is linear, i.e. 'relative risk' is constant. Absolute benefit is then proportional to a patient's baseline risk and th...

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Autores principales: Wang, Hao, Boissel, Jean-Pierre, Nony, Patrice
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646709/
https://www.ncbi.nlm.nih.gov/pubmed/19222846
http://dx.doi.org/10.1186/1742-7622-6-1
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author Wang, Hao
Boissel, Jean-Pierre
Nony, Patrice
author_facet Wang, Hao
Boissel, Jean-Pierre
Nony, Patrice
author_sort Wang, Hao
collection PubMed
description BACKGROUND: In medical practice, it is generally accepted that the 'effect model' describing the relationship between baseline risk and risk under treatment is linear, i.e. 'relative risk' is constant. Absolute benefit is then proportional to a patient's baseline risk and the treatment is most effective among high-risk patients. Alternatively, the 'effect model' becomes curvilinear when 'odds ratio' is considered to be constant. However these two models are based on purely empirical considerations, and there is still no theoretical approach to support either the linear or the non-linear relation. PRESENTATION OF THE HYPOTHESIS: From logistic and sigmoidal Emax (Hill) models, we derived a phenomenological model which includes the possibility of integrating both beneficial and harmful effects. Instead of a linear relation, our model suggests that the relationship is curvilinear i.e. the moderate-risk patients gain most from the treatment in opposition to those with low or high risk. TESTING THE HYPOTHESIS: Two approaches can be proposed to investigate in practice such a model. The retrospective one is to perform a meta-analysis of clinical trials with subgroups of patients including a great range of baseline risks. The prospective one is to perform a large clinical trial in which patients are recruited according to several prestratified diverse and high risk groups. IMPLICATIONS OF THE HYPOTHESIS: For the quantification of the treatment effect and considering such a model, the discrepancy between odds ratio and relative risk may be related not only to the level of risk under control conditions, but also to the characteristics of the dose-effect relation and the amount of dose administered. In the proposed approach, OR may be considered as constant in the whole range of Rc, and depending only on the intrinsic characteristics of the treatment. Therefore, OR should be preferred rather than RR to summarize information on treatment efficacy.
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spelling pubmed-26467092009-02-24 Revisiting the relationship between baseline risk and risk under treatment Wang, Hao Boissel, Jean-Pierre Nony, Patrice Emerg Themes Epidemiol Hypothesis BACKGROUND: In medical practice, it is generally accepted that the 'effect model' describing the relationship between baseline risk and risk under treatment is linear, i.e. 'relative risk' is constant. Absolute benefit is then proportional to a patient's baseline risk and the treatment is most effective among high-risk patients. Alternatively, the 'effect model' becomes curvilinear when 'odds ratio' is considered to be constant. However these two models are based on purely empirical considerations, and there is still no theoretical approach to support either the linear or the non-linear relation. PRESENTATION OF THE HYPOTHESIS: From logistic and sigmoidal Emax (Hill) models, we derived a phenomenological model which includes the possibility of integrating both beneficial and harmful effects. Instead of a linear relation, our model suggests that the relationship is curvilinear i.e. the moderate-risk patients gain most from the treatment in opposition to those with low or high risk. TESTING THE HYPOTHESIS: Two approaches can be proposed to investigate in practice such a model. The retrospective one is to perform a meta-analysis of clinical trials with subgroups of patients including a great range of baseline risks. The prospective one is to perform a large clinical trial in which patients are recruited according to several prestratified diverse and high risk groups. IMPLICATIONS OF THE HYPOTHESIS: For the quantification of the treatment effect and considering such a model, the discrepancy between odds ratio and relative risk may be related not only to the level of risk under control conditions, but also to the characteristics of the dose-effect relation and the amount of dose administered. In the proposed approach, OR may be considered as constant in the whole range of Rc, and depending only on the intrinsic characteristics of the treatment. Therefore, OR should be preferred rather than RR to summarize information on treatment efficacy. BioMed Central 2009-02-17 /pmc/articles/PMC2646709/ /pubmed/19222846 http://dx.doi.org/10.1186/1742-7622-6-1 Text en Copyright © 2009 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Wang, Hao
Boissel, Jean-Pierre
Nony, Patrice
Revisiting the relationship between baseline risk and risk under treatment
title Revisiting the relationship between baseline risk and risk under treatment
title_full Revisiting the relationship between baseline risk and risk under treatment
title_fullStr Revisiting the relationship between baseline risk and risk under treatment
title_full_unstemmed Revisiting the relationship between baseline risk and risk under treatment
title_short Revisiting the relationship between baseline risk and risk under treatment
title_sort revisiting the relationship between baseline risk and risk under treatment
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646709/
https://www.ncbi.nlm.nih.gov/pubmed/19222846
http://dx.doi.org/10.1186/1742-7622-6-1
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