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An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial

BACKGROUND: Decisions about new health technologies are increasingly being made while trials are still in an early stage, which may result in substantial uncertainty around key decision drivers such as estimates of life expectancy and time to disease progression. Additional data collection can reduc...

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Autores principales: Vervaart, Mathyn, Strong, Mark, Claxton, Karl P., Welton, Nicky J., Wisløff, Torbjørn, Aas, Eline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189722/
https://www.ncbi.nlm.nih.gov/pubmed/34967237
http://dx.doi.org/10.1177/0272989X211068019
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author Vervaart, Mathyn
Strong, Mark
Claxton, Karl P.
Welton, Nicky J.
Wisløff, Torbjørn
Aas, Eline
author_facet Vervaart, Mathyn
Strong, Mark
Claxton, Karl P.
Welton, Nicky J.
Wisløff, Torbjørn
Aas, Eline
author_sort Vervaart, Mathyn
collection PubMed
description BACKGROUND: Decisions about new health technologies are increasingly being made while trials are still in an early stage, which may result in substantial uncertainty around key decision drivers such as estimates of life expectancy and time to disease progression. Additional data collection can reduce uncertainty, and its value can be quantified by computing the expected value of sample information (EVSI), which has typically been described in the context of designing a future trial. In this article, we develop new methods for computing the EVSI of extending an existing trial’s follow-up, first for an assumed survival model and then extending to capture uncertainty about the true survival model. METHODS: We developed a nested Markov Chain Monte Carlo procedure and a nonparametric regression-based method. We compared the methods by computing single-model and model-averaged EVSI for collecting additional follow-up data in 2 synthetic case studies. RESULTS: There was good agreement between the 2 methods. The regression-based method was fast and straightforward to implement, and scales easily to include any number of candidate survival models in the model uncertainty case. The nested Monte Carlo procedure, on the other hand, was extremely computationally demanding when we included model uncertainty. CONCLUSIONS: We present a straightforward regression-based method for computing the EVSI of extending an existing trial’s follow-up, both where a single known survival model is assumed and where we are uncertain about the true survival model. EVSI for ongoing trials can help decision makers determine whether early patient access to a new technology can be justified on the basis of the current evidence or whether more mature evidence is needed. HIGHLIGHTS: Decisions about new health technologies are increasingly being made while trials are still in an early stage, which may result in substantial uncertainty around key decision drivers such as estimates of life-expectancy and time to disease progression. Additional data collection can reduce uncertainty, and its value can be quantified by computing the expected value of sample information (EVSI), which has typically been described in the context of designing a future trial. In this article, we have developed new methods for computing the EVSI of extending a trial’s follow-up, both where a single known survival model is assumed and where we are uncertain about the true survival model. We extend a previously described nonparametric regression-based method for computing EVSI, which we demonstrate in synthetic case studies is fast, straightforward to implement, and scales easily to include any number of candidate survival models in the EVSI calculations. The EVSI methods that we present in this article can quantify the need for collecting additional follow-up data before making an adoption decision given any decision-making context.
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spelling pubmed-91897222022-06-14 An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial Vervaart, Mathyn Strong, Mark Claxton, Karl P. Welton, Nicky J. Wisløff, Torbjørn Aas, Eline Med Decis Making Original Research Articles BACKGROUND: Decisions about new health technologies are increasingly being made while trials are still in an early stage, which may result in substantial uncertainty around key decision drivers such as estimates of life expectancy and time to disease progression. Additional data collection can reduce uncertainty, and its value can be quantified by computing the expected value of sample information (EVSI), which has typically been described in the context of designing a future trial. In this article, we develop new methods for computing the EVSI of extending an existing trial’s follow-up, first for an assumed survival model and then extending to capture uncertainty about the true survival model. METHODS: We developed a nested Markov Chain Monte Carlo procedure and a nonparametric regression-based method. We compared the methods by computing single-model and model-averaged EVSI for collecting additional follow-up data in 2 synthetic case studies. RESULTS: There was good agreement between the 2 methods. The regression-based method was fast and straightforward to implement, and scales easily to include any number of candidate survival models in the model uncertainty case. The nested Monte Carlo procedure, on the other hand, was extremely computationally demanding when we included model uncertainty. CONCLUSIONS: We present a straightforward regression-based method for computing the EVSI of extending an existing trial’s follow-up, both where a single known survival model is assumed and where we are uncertain about the true survival model. EVSI for ongoing trials can help decision makers determine whether early patient access to a new technology can be justified on the basis of the current evidence or whether more mature evidence is needed. HIGHLIGHTS: Decisions about new health technologies are increasingly being made while trials are still in an early stage, which may result in substantial uncertainty around key decision drivers such as estimates of life-expectancy and time to disease progression. Additional data collection can reduce uncertainty, and its value can be quantified by computing the expected value of sample information (EVSI), which has typically been described in the context of designing a future trial. In this article, we have developed new methods for computing the EVSI of extending a trial’s follow-up, both where a single known survival model is assumed and where we are uncertain about the true survival model. We extend a previously described nonparametric regression-based method for computing EVSI, which we demonstrate in synthetic case studies is fast, straightforward to implement, and scales easily to include any number of candidate survival models in the EVSI calculations. The EVSI methods that we present in this article can quantify the need for collecting additional follow-up data before making an adoption decision given any decision-making context. SAGE Publications 2021-12-30 2022-07 /pmc/articles/PMC9189722/ /pubmed/34967237 http://dx.doi.org/10.1177/0272989X211068019 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any 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
Vervaart, Mathyn
Strong, Mark
Claxton, Karl P.
Welton, Nicky J.
Wisløff, Torbjørn
Aas, Eline
An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title_full An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title_fullStr An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title_full_unstemmed An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title_short An Efficient Method for Computing Expected Value of Sample Information for Survival Data from an Ongoing Trial
title_sort efficient method for computing expected value of sample information for survival data from an ongoing trial
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189722/
https://www.ncbi.nlm.nih.gov/pubmed/34967237
http://dx.doi.org/10.1177/0272989X211068019
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