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Decision Curve Analysis for Personalized Treatment Choice between Multiple Options

BACKGROUND: Decision curve analysis can be used to determine whether a personalized model for treatment benefit would lead to better clinical decisions. Decision curve analysis methods have been described to estimate treatment benefit using data from a single randomized controlled trial. OBJECTIVES:...

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Autores principales: Chalkou, Konstantina, Vickers, Andrew J., Pellegrini, Fabio, Manca, Andrea, Salanti, Georgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021120/
https://www.ncbi.nlm.nih.gov/pubmed/36511470
http://dx.doi.org/10.1177/0272989X221143058
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author Chalkou, Konstantina
Vickers, Andrew J.
Pellegrini, Fabio
Manca, Andrea
Salanti, Georgia
author_facet Chalkou, Konstantina
Vickers, Andrew J.
Pellegrini, Fabio
Manca, Andrea
Salanti, Georgia
author_sort Chalkou, Konstantina
collection PubMed
description BACKGROUND: Decision curve analysis can be used to determine whether a personalized model for treatment benefit would lead to better clinical decisions. Decision curve analysis methods have been described to estimate treatment benefit using data from a single randomized controlled trial. OBJECTIVES: Our main objective is to extend the decision curve analysis methodology to the scenario in which several treatment options exist and evidence about their effects comes from a set of trials, synthesized using network meta-analysis (NMA). METHODS: We describe the steps needed to estimate the net benefit of a prediction model using evidence from studies synthesized in an NMA. We show how to compare personalized versus one-size-fit-all treatment decision-making strategies, such as “treat none” or “treat all patients with a specific treatment” strategies. First, threshold values for each included treatment need to be defined (i.e., the minimum risk difference compared with control that renders a treatment worth taking). The net benefit per strategy can then be plotted for a plausible range of threshold values to reveal the most clinically useful strategy. We applied our methodology to an NMA prediction model for relapsing-remitting multiple sclerosis, which can be used to choose between natalizumab, dimethyl fumarate, glatiramer acetate, and placebo. RESULTS: We illustrated the extended decision curve analysis methodology using several threshold value combinations for each available treatment. For the examined threshold values, the “treat patients according to the prediction model” strategy performs either better than or close to the one-size-fit-all treatment strategies. However, even small differences may be important in clinical decision making. As the advantage of the personalized model was not consistent across all thresholds, improving the existing model (by including, for example, predictors that will increase discrimination) is needed before advocating its clinical usefulness. CONCLUSIONS: This novel extension of decision curve analysis can be applied to NMA-based prediction models to evaluate their use to aid treatment decision making. HIGHLIGHTS: Decision curve analysis is extended into a (network) meta-analysis framework. Personalized models predicting treatment benefit are evaluated when several treatment options are available and evidence about their effects comes from a set of trials. Detailed steps to compare personalized versus one-size-fit-all treatment decision-making strategies are outlined. This extension of decision curve analysis can be applied to (network) meta-analysis–based prediction models to evaluate their use to aid treatment decision making.
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spelling pubmed-100211202023-03-18 Decision Curve Analysis for Personalized Treatment Choice between Multiple Options Chalkou, Konstantina Vickers, Andrew J. Pellegrini, Fabio Manca, Andrea Salanti, Georgia Med Decis Making Original Research Articles BACKGROUND: Decision curve analysis can be used to determine whether a personalized model for treatment benefit would lead to better clinical decisions. Decision curve analysis methods have been described to estimate treatment benefit using data from a single randomized controlled trial. OBJECTIVES: Our main objective is to extend the decision curve analysis methodology to the scenario in which several treatment options exist and evidence about their effects comes from a set of trials, synthesized using network meta-analysis (NMA). METHODS: We describe the steps needed to estimate the net benefit of a prediction model using evidence from studies synthesized in an NMA. We show how to compare personalized versus one-size-fit-all treatment decision-making strategies, such as “treat none” or “treat all patients with a specific treatment” strategies. First, threshold values for each included treatment need to be defined (i.e., the minimum risk difference compared with control that renders a treatment worth taking). The net benefit per strategy can then be plotted for a plausible range of threshold values to reveal the most clinically useful strategy. We applied our methodology to an NMA prediction model for relapsing-remitting multiple sclerosis, which can be used to choose between natalizumab, dimethyl fumarate, glatiramer acetate, and placebo. RESULTS: We illustrated the extended decision curve analysis methodology using several threshold value combinations for each available treatment. For the examined threshold values, the “treat patients according to the prediction model” strategy performs either better than or close to the one-size-fit-all treatment strategies. However, even small differences may be important in clinical decision making. As the advantage of the personalized model was not consistent across all thresholds, improving the existing model (by including, for example, predictors that will increase discrimination) is needed before advocating its clinical usefulness. CONCLUSIONS: This novel extension of decision curve analysis can be applied to NMA-based prediction models to evaluate their use to aid treatment decision making. HIGHLIGHTS: Decision curve analysis is extended into a (network) meta-analysis framework. Personalized models predicting treatment benefit are evaluated when several treatment options are available and evidence about their effects comes from a set of trials. Detailed steps to compare personalized versus one-size-fit-all treatment decision-making strategies are outlined. This extension of decision curve analysis can be applied to (network) meta-analysis–based prediction models to evaluate their use to aid treatment decision making. SAGE Publications 2022-12-13 2023-04 /pmc/articles/PMC10021120/ /pubmed/36511470 http://dx.doi.org/10.1177/0272989X221143058 Text en © The Author(s) 2022 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Articles
Chalkou, Konstantina
Vickers, Andrew J.
Pellegrini, Fabio
Manca, Andrea
Salanti, Georgia
Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title_full Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title_fullStr Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title_full_unstemmed Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title_short Decision Curve Analysis for Personalized Treatment Choice between Multiple Options
title_sort decision curve analysis for personalized treatment choice between multiple options
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021120/
https://www.ncbi.nlm.nih.gov/pubmed/36511470
http://dx.doi.org/10.1177/0272989X221143058
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