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Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease
BACKGROUND: The need for preventive therapies that interrupt the progression of Alzheimer’s disease (AD) before the onset of symptoms or when symptoms are emerging is urgent and has spurred the ongoing development of disease-modifying therapies (DMTs) in preclinical and early AD (mild cognitive impa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017027/ https://www.ncbi.nlm.nih.gov/pubmed/35440022 http://dx.doi.org/10.1186/s13195-022-00984-y |
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author | Assunção, Sheila Seleri Sperling, Reisa A. Ritchie, Craig Kerwin, Diana R. Aisen, Paul S. Lansdall, Claire Atri, Alireza Cummings, Jeffrey |
author_facet | Assunção, Sheila Seleri Sperling, Reisa A. Ritchie, Craig Kerwin, Diana R. Aisen, Paul S. Lansdall, Claire Atri, Alireza Cummings, Jeffrey |
author_sort | Assunção, Sheila Seleri |
collection | PubMed |
description | BACKGROUND: The need for preventive therapies that interrupt the progression of Alzheimer’s disease (AD) before the onset of symptoms or when symptoms are emerging is urgent and has spurred the ongoing development of disease-modifying therapies (DMTs) in preclinical and early AD (mild cognitive impairment [MCI] to mild dementia). Assessing the meaningfulness of what are likely small initial treatment effects in these earlier stages of the AD patho-clinical disease continuum is a major challenge and warrants further consideration. BODY: To accommodate a shift towards earlier intervention in AD, we propose meaningful benefits as a new umbrella concept that encapsulates the spectrum of potentially desirable outcomes that may be demonstrated in clinical trials and other studies across the AD continuum, with an emphasis on preclinical AD and early AD (i.e., MCI due to AD and mild AD dementia). The meaningful benefits framework applies to data collection, assessment, and communication across three dimensions: (1) multidimensional clinical outcome assessments (COAs) including not only core disease outcomes related to cognition and function but also patient- and caregiver-reported outcomes, health and economic outcomes, and neuropsychiatric symptoms; (2) complementary analyses that help contextualize and expand the understanding of COA-based assessments, such as number-needed-to-treat or time-to-event analyses; and (3) assessment of both cumulative benefit and predictive benefit, where early changes on cognitive, functional, or biomarker assessments predict longer-term clinical benefit. CONCLUSION: The concept of meaningful benefits emphasizes the importance of multidimensional reporting of clinical trial data while, conceptually, it advances our understanding of treatment effects in preclinical AD and mild cognitive impairment due to AD. We propose that such an approach will help bridge the gap between the emergence of DMTs and their clinical use, particularly now that a DMT is available for patients diagnosed with MCI due to AD and mild AD dementia. |
format | Online Article Text |
id | pubmed-9017027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90170272022-04-20 Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease Assunção, Sheila Seleri Sperling, Reisa A. Ritchie, Craig Kerwin, Diana R. Aisen, Paul S. Lansdall, Claire Atri, Alireza Cummings, Jeffrey Alzheimers Res Ther Review BACKGROUND: The need for preventive therapies that interrupt the progression of Alzheimer’s disease (AD) before the onset of symptoms or when symptoms are emerging is urgent and has spurred the ongoing development of disease-modifying therapies (DMTs) in preclinical and early AD (mild cognitive impairment [MCI] to mild dementia). Assessing the meaningfulness of what are likely small initial treatment effects in these earlier stages of the AD patho-clinical disease continuum is a major challenge and warrants further consideration. BODY: To accommodate a shift towards earlier intervention in AD, we propose meaningful benefits as a new umbrella concept that encapsulates the spectrum of potentially desirable outcomes that may be demonstrated in clinical trials and other studies across the AD continuum, with an emphasis on preclinical AD and early AD (i.e., MCI due to AD and mild AD dementia). The meaningful benefits framework applies to data collection, assessment, and communication across three dimensions: (1) multidimensional clinical outcome assessments (COAs) including not only core disease outcomes related to cognition and function but also patient- and caregiver-reported outcomes, health and economic outcomes, and neuropsychiatric symptoms; (2) complementary analyses that help contextualize and expand the understanding of COA-based assessments, such as number-needed-to-treat or time-to-event analyses; and (3) assessment of both cumulative benefit and predictive benefit, where early changes on cognitive, functional, or biomarker assessments predict longer-term clinical benefit. CONCLUSION: The concept of meaningful benefits emphasizes the importance of multidimensional reporting of clinical trial data while, conceptually, it advances our understanding of treatment effects in preclinical AD and mild cognitive impairment due to AD. We propose that such an approach will help bridge the gap between the emergence of DMTs and their clinical use, particularly now that a DMT is available for patients diagnosed with MCI due to AD and mild AD dementia. BioMed Central 2022-04-19 /pmc/articles/PMC9017027/ /pubmed/35440022 http://dx.doi.org/10.1186/s13195-022-00984-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Assunção, Sheila Seleri Sperling, Reisa A. Ritchie, Craig Kerwin, Diana R. Aisen, Paul S. Lansdall, Claire Atri, Alireza Cummings, Jeffrey Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title | Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title_full | Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title_fullStr | Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title_full_unstemmed | Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title_short | Meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early Alzheimer’s disease |
title_sort | meaningful benefits: a framework to assess disease-modifying therapies in preclinical and early alzheimer’s disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017027/ https://www.ncbi.nlm.nih.gov/pubmed/35440022 http://dx.doi.org/10.1186/s13195-022-00984-y |
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