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Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies

In the era of rapid development of new, expensive cancer therapies, value frameworks have been developed to quantify clinical benefit (CB). We assessed the evolution of CB since the 2015 introduction of The American Society of Clinical Oncology and The European Society of Medical Oncology value fram...

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Autores principales: Cusano, Ellen, Wong, Chelsea, Taguedong, Eddy, Vaska, Marcus, Abedin, Tasnima, Nixon, Nancy, Karim, Safiya, Tang, Patricia, Heng, Daniel Y. C., Ezeife, Doreen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628676/
https://www.ncbi.nlm.nih.gov/pubmed/34898590
http://dx.doi.org/10.3390/curroncol28060412
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author Cusano, Ellen
Wong, Chelsea
Taguedong, Eddy
Vaska, Marcus
Abedin, Tasnima
Nixon, Nancy
Karim, Safiya
Tang, Patricia
Heng, Daniel Y. C.
Ezeife, Doreen
author_facet Cusano, Ellen
Wong, Chelsea
Taguedong, Eddy
Vaska, Marcus
Abedin, Tasnima
Nixon, Nancy
Karim, Safiya
Tang, Patricia
Heng, Daniel Y. C.
Ezeife, Doreen
author_sort Cusano, Ellen
collection PubMed
description In the era of rapid development of new, expensive cancer therapies, value frameworks have been developed to quantify clinical benefit (CB). We assessed the evolution of CB since the 2015 introduction of The American Society of Clinical Oncology and The European Society of Medical Oncology value frameworks. Randomized clinical trials (RCTs) assessing systemic therapies for solid malignancies from 2010 to 2020 were evaluated and CB (Δ) in 2010–2014 (pre-value frameworks (PRE)) were compared to 2015–2020 (POST) for overall survival (OS), progression-free survival (PFS), response rate (RR), and quality of life (QoL). In the 485 studies analyzed (12% PRE and 88% POST), the most common primary endpoint was PFS (49%), followed by OS (20%), RR (12%), and QoL (6%), with a significant increase in OS and decrease in RR as primary endpoints in the POST era (p = 0.011). Multivariable analyses revealed significant improvement in ΔOS POST (OR 2.86, 95% CI 0.46 to 5.26, p = 0.02) while controlling for other variables. After the development of value frameworks, median ΔOS improved minimally. The impact of value frameworks has yet to be fully realized in RCTs. Efforts to include endpoints shown to impact value, such as QoL, into clinical trials are warranted.
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spelling pubmed-86286762021-11-30 Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies Cusano, Ellen Wong, Chelsea Taguedong, Eddy Vaska, Marcus Abedin, Tasnima Nixon, Nancy Karim, Safiya Tang, Patricia Heng, Daniel Y. C. Ezeife, Doreen Curr Oncol Article In the era of rapid development of new, expensive cancer therapies, value frameworks have been developed to quantify clinical benefit (CB). We assessed the evolution of CB since the 2015 introduction of The American Society of Clinical Oncology and The European Society of Medical Oncology value frameworks. Randomized clinical trials (RCTs) assessing systemic therapies for solid malignancies from 2010 to 2020 were evaluated and CB (Δ) in 2010–2014 (pre-value frameworks (PRE)) were compared to 2015–2020 (POST) for overall survival (OS), progression-free survival (PFS), response rate (RR), and quality of life (QoL). In the 485 studies analyzed (12% PRE and 88% POST), the most common primary endpoint was PFS (49%), followed by OS (20%), RR (12%), and QoL (6%), with a significant increase in OS and decrease in RR as primary endpoints in the POST era (p = 0.011). Multivariable analyses revealed significant improvement in ΔOS POST (OR 2.86, 95% CI 0.46 to 5.26, p = 0.02) while controlling for other variables. After the development of value frameworks, median ΔOS improved minimally. The impact of value frameworks has yet to be fully realized in RCTs. Efforts to include endpoints shown to impact value, such as QoL, into clinical trials are warranted. MDPI 2021-11-21 /pmc/articles/PMC8628676/ /pubmed/34898590 http://dx.doi.org/10.3390/curroncol28060412 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cusano, Ellen
Wong, Chelsea
Taguedong, Eddy
Vaska, Marcus
Abedin, Tasnima
Nixon, Nancy
Karim, Safiya
Tang, Patricia
Heng, Daniel Y. C.
Ezeife, Doreen
Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title_full Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title_fullStr Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title_full_unstemmed Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title_short Impact of Value Frameworks on the Magnitude of Clinical Benefit: Evaluating a Decade of Randomized Trials for Systemic Therapy in Solid Malignancies
title_sort impact of value frameworks on the magnitude of clinical benefit: evaluating a decade of randomized trials for systemic therapy in solid malignancies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628676/
https://www.ncbi.nlm.nih.gov/pubmed/34898590
http://dx.doi.org/10.3390/curroncol28060412
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