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Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials

OBJECTIVES: The COVID-19 pandemic necessitates time-sensitive policy and implementation decisions regarding new therapies in the face of uncertainty. This study aimed to quantify consequences of approving therapies or pursuing further research: immediate approval, use only in research, approval with...

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Autores principales: Dijk, Stijntje W., Krijkamp, Eline M., Kunst, Natalia, Gross, Cary P., Wong, John B., Hunink, M.G. Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Society for Pharmacoeconomics and Outcomes Research, Inc. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045876/
https://www.ncbi.nlm.nih.gov/pubmed/35490085
http://dx.doi.org/10.1016/j.jval.2022.03.016
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author Dijk, Stijntje W.
Krijkamp, Eline M.
Kunst, Natalia
Gross, Cary P.
Wong, John B.
Hunink, M.G. Myriam
author_facet Dijk, Stijntje W.
Krijkamp, Eline M.
Kunst, Natalia
Gross, Cary P.
Wong, John B.
Hunink, M.G. Myriam
author_sort Dijk, Stijntje W.
collection PubMed
description OBJECTIVES: The COVID-19 pandemic necessitates time-sensitive policy and implementation decisions regarding new therapies in the face of uncertainty. This study aimed to quantify consequences of approving therapies or pursuing further research: immediate approval, use only in research, approval with research (eg, emergency use authorization), or reject. METHODS: Using a cohort state-transition model for hospitalized patients with COVID-19, we estimated quality-adjusted life-years (QALYs) and costs associated with the following interventions: hydroxychloroquine, remdesivir, casirivimab-imdevimab, dexamethasone, baricitinib-remdesivir, tocilizumab, lopinavir-ritonavir, interferon beta-1a, and usual care. We used the model outcomes to conduct cost-effectiveness and value of information analyses from a US healthcare perspective and a lifetime horizon. RESULTS: Assuming a $100 000-per-QALY willingness-to-pay threshold, only remdesivir, casirivimab-imdevimab, dexamethasone, baricitinib-remdesivir, and tocilizumab were (cost-) effective (incremental net health benefit 0.252, 0.164, 0.545, 0.668, and 0.524 QALYs and incremental net monetary benefit $25 249, $16 375, $54 526, $66 826, and $52 378). Our value of information analyses suggest that most value can be obtained if these 5 therapies are approved for immediate use rather than requiring additional randomized controlled trials (RCTs) (net value $20.6 billion, $13.4 billion, $7.4 billion, $54.6 billion, and $7.1 billion), hydroxychloroquine (net value $198 million) is only used in further RCTs if seeking to demonstrate decremental cost-effectiveness and otherwise rejected, and interferon beta-1a and lopinavir-ritonavir are rejected (ie, neither approved nor additional RCTs). CONCLUSIONS: Estimating the real-time value of collecting additional evidence during the pandemic can inform policy makers and clinicians about the optimal moment to implement therapies and whether to perform further research.
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spelling pubmed-90458762022-04-28 Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials Dijk, Stijntje W. Krijkamp, Eline M. Kunst, Natalia Gross, Cary P. Wong, John B. Hunink, M.G. Myriam Value Health Themed Section: COVID-19 OBJECTIVES: The COVID-19 pandemic necessitates time-sensitive policy and implementation decisions regarding new therapies in the face of uncertainty. This study aimed to quantify consequences of approving therapies or pursuing further research: immediate approval, use only in research, approval with research (eg, emergency use authorization), or reject. METHODS: Using a cohort state-transition model for hospitalized patients with COVID-19, we estimated quality-adjusted life-years (QALYs) and costs associated with the following interventions: hydroxychloroquine, remdesivir, casirivimab-imdevimab, dexamethasone, baricitinib-remdesivir, tocilizumab, lopinavir-ritonavir, interferon beta-1a, and usual care. We used the model outcomes to conduct cost-effectiveness and value of information analyses from a US healthcare perspective and a lifetime horizon. RESULTS: Assuming a $100 000-per-QALY willingness-to-pay threshold, only remdesivir, casirivimab-imdevimab, dexamethasone, baricitinib-remdesivir, and tocilizumab were (cost-) effective (incremental net health benefit 0.252, 0.164, 0.545, 0.668, and 0.524 QALYs and incremental net monetary benefit $25 249, $16 375, $54 526, $66 826, and $52 378). Our value of information analyses suggest that most value can be obtained if these 5 therapies are approved for immediate use rather than requiring additional randomized controlled trials (RCTs) (net value $20.6 billion, $13.4 billion, $7.4 billion, $54.6 billion, and $7.1 billion), hydroxychloroquine (net value $198 million) is only used in further RCTs if seeking to demonstrate decremental cost-effectiveness and otherwise rejected, and interferon beta-1a and lopinavir-ritonavir are rejected (ie, neither approved nor additional RCTs). CONCLUSIONS: Estimating the real-time value of collecting additional evidence during the pandemic can inform policy makers and clinicians about the optimal moment to implement therapies and whether to perform further research. International Society for Pharmacoeconomics and Outcomes Research, Inc. Published by Elsevier Inc. 2022-08 2022-04-28 /pmc/articles/PMC9045876/ /pubmed/35490085 http://dx.doi.org/10.1016/j.jval.2022.03.016 Text en © 2022 International Society for Pharmacoeconomics and Outcomes Research, Inc. Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Themed Section: COVID-19
Dijk, Stijntje W.
Krijkamp, Eline M.
Kunst, Natalia
Gross, Cary P.
Wong, John B.
Hunink, M.G. Myriam
Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title_full Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title_fullStr Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title_full_unstemmed Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title_short Emerging Therapies for COVID-19: The Value of Information From More Clinical Trials
title_sort emerging therapies for covid-19: the value of information from more clinical trials
topic Themed Section: COVID-19
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045876/
https://www.ncbi.nlm.nih.gov/pubmed/35490085
http://dx.doi.org/10.1016/j.jval.2022.03.016
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