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Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions

Background and Objectives. Risk-tolerance measures from patient-preference studies typically focus on individual adverse events. We recently introduced an approach that extends maximum acceptable risk (MAR) calculations to simultaneous maximum acceptable risk thresholds (SMART) for multiple treatmen...

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Autores principales: Montano-Campos, J. Felipe, Gonzalez, Juan Marcos, Rickert, Timothy, Fairchild, Angelyn O., Levitan, Bennett, Reed, Shelby D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841858/
https://www.ncbi.nlm.nih.gov/pubmed/36654678
http://dx.doi.org/10.1177/23814683221148715
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author Montano-Campos, J. Felipe
Gonzalez, Juan Marcos
Rickert, Timothy
Fairchild, Angelyn O.
Levitan, Bennett
Reed, Shelby D.
author_facet Montano-Campos, J. Felipe
Gonzalez, Juan Marcos
Rickert, Timothy
Fairchild, Angelyn O.
Levitan, Bennett
Reed, Shelby D.
author_sort Montano-Campos, J. Felipe
collection PubMed
description Background and Objectives. Risk-tolerance measures from patient-preference studies typically focus on individual adverse events. We recently introduced an approach that extends maximum acceptable risk (MAR) calculations to simultaneous maximum acceptable risk thresholds (SMART) for multiple treatment-related risks. We extend these methods to include the computation and display of confidence intervals and apply the approach to 3 published discrete-choice experiments to evaluate its utility to inform regulatory decisions. Methods. We generate MAR estimates and SMART curves and compare them with trial-based benefit-risk profiles of select treatments for depression, psoriasis, and thyroid cancer. Results. In the depression study, SMART curves with 70% to 95% confidence intervals portray which combinations of 2 adverse events would be considered acceptable. In the psoriasis example, the asymmetric confidence intervals for the SMART curve indicate that relying on independent MARs versus SMART curves when there are nonlinear preferences can lead to decisions that could expose patients to greater risks than they would accept. The thyroid cancer application shows an example in which the clinical incidence of each of 3 adverse events is lower than the single-event MARs for the expected treatment benefit, yet the collective risk profile surpasses acceptable levels when considered jointly. Limitations. Nonrandom sample of studies. Conclusions. When evaluating conventional MARs in which the observed incidences are near the estimated MARs or where preferences demonstrate diminishing marginal disutility of risk, conventional MAR estimates will overstate risk acceptance, which could lead to misinformed decisions, potentially placing patients at greater risk of adverse events than they would accept. Implications. The SMART method, herein extended to include confidence intervals, provides a reproducible, transparent evidence-based approach to enable decision makers to use data from discrete-choice experiments to account for multiple adverse events. HIGHLIGHTS: Estimates of maximum acceptable risk (MAR) for a defined treatment benefit can be useful to inform regulatory decisions; however, the conventional metric considers one adverse event at a time. This article applies a new approach known as SMART (simultaneous maximum acceptable risk thresholds) that accounts for multiple adverse events to 3 published discrete-choice experiments. Findings reveal that conventional MARs could lead decision makers to accept a treatment based on individual risks that would not be acceptable if multiple risks are considered simultaneously.
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spelling pubmed-98418582023-01-17 Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions Montano-Campos, J. Felipe Gonzalez, Juan Marcos Rickert, Timothy Fairchild, Angelyn O. Levitan, Bennett Reed, Shelby D. MDM Policy Pract Original Research Article Background and Objectives. Risk-tolerance measures from patient-preference studies typically focus on individual adverse events. We recently introduced an approach that extends maximum acceptable risk (MAR) calculations to simultaneous maximum acceptable risk thresholds (SMART) for multiple treatment-related risks. We extend these methods to include the computation and display of confidence intervals and apply the approach to 3 published discrete-choice experiments to evaluate its utility to inform regulatory decisions. Methods. We generate MAR estimates and SMART curves and compare them with trial-based benefit-risk profiles of select treatments for depression, psoriasis, and thyroid cancer. Results. In the depression study, SMART curves with 70% to 95% confidence intervals portray which combinations of 2 adverse events would be considered acceptable. In the psoriasis example, the asymmetric confidence intervals for the SMART curve indicate that relying on independent MARs versus SMART curves when there are nonlinear preferences can lead to decisions that could expose patients to greater risks than they would accept. The thyroid cancer application shows an example in which the clinical incidence of each of 3 adverse events is lower than the single-event MARs for the expected treatment benefit, yet the collective risk profile surpasses acceptable levels when considered jointly. Limitations. Nonrandom sample of studies. Conclusions. When evaluating conventional MARs in which the observed incidences are near the estimated MARs or where preferences demonstrate diminishing marginal disutility of risk, conventional MAR estimates will overstate risk acceptance, which could lead to misinformed decisions, potentially placing patients at greater risk of adverse events than they would accept. Implications. The SMART method, herein extended to include confidence intervals, provides a reproducible, transparent evidence-based approach to enable decision makers to use data from discrete-choice experiments to account for multiple adverse events. HIGHLIGHTS: Estimates of maximum acceptable risk (MAR) for a defined treatment benefit can be useful to inform regulatory decisions; however, the conventional metric considers one adverse event at a time. This article applies a new approach known as SMART (simultaneous maximum acceptable risk thresholds) that accounts for multiple adverse events to 3 published discrete-choice experiments. Findings reveal that conventional MARs could lead decision makers to accept a treatment based on individual risks that would not be acceptable if multiple risks are considered simultaneously. SAGE Publications 2023-01-11 /pmc/articles/PMC9841858/ /pubmed/36654678 http://dx.doi.org/10.1177/23814683221148715 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Montano-Campos, J. Felipe
Gonzalez, Juan Marcos
Rickert, Timothy
Fairchild, Angelyn O.
Levitan, Bennett
Reed, Shelby D.
Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title_full Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title_fullStr Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title_full_unstemmed Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title_short Use of Patient Preferences Data Regarding Multiple Risks to Inform Regulatory Decisions
title_sort use of patient preferences data regarding multiple risks to inform regulatory decisions
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841858/
https://www.ncbi.nlm.nih.gov/pubmed/36654678
http://dx.doi.org/10.1177/23814683221148715
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