Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.

BACKGROUND: Although several mathematical models have been proposed to assess the risk:benefit of drugs in one measure, their use in practice has been rather limited. Our objective was to design a simple, easily applicable model. In this respect, measuring the proportion of patients who respond favo...

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Main Authors: José N Boada, Carlos Boada, Mar García-Sáiz, Marcelino García, Eduardo Fernández, Eugenio Gómez
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2570485?pdf=render
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author José N Boada
Carlos Boada
Mar García-Sáiz
Marcelino García
Eduardo Fernández
Eugenio Gómez
author_facet José N Boada
Carlos Boada
Mar García-Sáiz
Marcelino García
Eduardo Fernández
Eugenio Gómez
author_sort José N Boada
collection DOAJ
description BACKGROUND: Although several mathematical models have been proposed to assess the risk:benefit of drugs in one measure, their use in practice has been rather limited. Our objective was to design a simple, easily applicable model. In this respect, measuring the proportion of patients who respond favorably to treatment without being affected by adverse drug reactions (ADR) could be a suitable endpoint. However, remarkably few published clinical trials report the data required to calculate this proportion. As an approach to the problem, we calculated the expected proportion of this type of patients. METHODOLOGY/PRINCIPAL FINDINGS: Theoretically, responders without ADR may be obtained by multiplying the total number of responders by the total number of subjects that did not suffer ADR, and dividing the product by the total number of subjects studied. When two drugs are studied, the same calculation may be repeated for the second drug. Then, by constructing a 2 x 2 table with the expected frequencies of responders with and without ADR, and non-responders with and without ADR, the odds ratio and relative risk with their confidence intervals may be easily calculated and graphically represented on a logarithmic scale. Such measures represent "net efficacy adjusted for risk" (NEAR). We assayed the model with results extracted from several published clinical trials or meta-analyses. On comparing our results with those originally reported by the authors, marked differences were found in some cases, with ADR arising as a relevant factor to balance the clinical benefit obtained. The particular features of the adverse reaction that must be weighed against benefit is discussed in the paper. CONCLUSION: NEAR representing overall risk-benefit may contribute to improving knowledge of drug clinical usefulness. As most published clinical trials tend to overestimate benefits and underestimate toxicity, our measure represents an effort to change this trend.
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spelling doaj.art-7911b8bcd9d74c0dba49f953229e2a2e2022-12-21T19:42:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-01310e358010.1371/journal.pone.0003580Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.José N BoadaCarlos BoadaMar García-SáizMarcelino GarcíaEduardo FernándezEugenio GómezBACKGROUND: Although several mathematical models have been proposed to assess the risk:benefit of drugs in one measure, their use in practice has been rather limited. Our objective was to design a simple, easily applicable model. In this respect, measuring the proportion of patients who respond favorably to treatment without being affected by adverse drug reactions (ADR) could be a suitable endpoint. However, remarkably few published clinical trials report the data required to calculate this proportion. As an approach to the problem, we calculated the expected proportion of this type of patients. METHODOLOGY/PRINCIPAL FINDINGS: Theoretically, responders without ADR may be obtained by multiplying the total number of responders by the total number of subjects that did not suffer ADR, and dividing the product by the total number of subjects studied. When two drugs are studied, the same calculation may be repeated for the second drug. Then, by constructing a 2 x 2 table with the expected frequencies of responders with and without ADR, and non-responders with and without ADR, the odds ratio and relative risk with their confidence intervals may be easily calculated and graphically represented on a logarithmic scale. Such measures represent "net efficacy adjusted for risk" (NEAR). We assayed the model with results extracted from several published clinical trials or meta-analyses. On comparing our results with those originally reported by the authors, marked differences were found in some cases, with ADR arising as a relevant factor to balance the clinical benefit obtained. The particular features of the adverse reaction that must be weighed against benefit is discussed in the paper. CONCLUSION: NEAR representing overall risk-benefit may contribute to improving knowledge of drug clinical usefulness. As most published clinical trials tend to overestimate benefits and underestimate toxicity, our measure represents an effort to change this trend.http://europepmc.org/articles/PMC2570485?pdf=render
spellingShingle José N Boada
Carlos Boada
Mar García-Sáiz
Marcelino García
Eduardo Fernández
Eugenio Gómez
Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
PLoS ONE
title Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
title_full Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
title_fullStr Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
title_full_unstemmed Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
title_short Net efficacy adjusted for risk (NEAR): a simple procedure for measuring risk:benefit balance.
title_sort net efficacy adjusted for risk near a simple procedure for measuring risk benefit balance
url http://europepmc.org/articles/PMC2570485?pdf=render
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