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Progression models for repeated measures : Estimating novel treatment effects in progressive diseases

Raket, Lars Lau LU orcid (2022) In Statistics in Medicine 41(28). p.5537-5557
Abstract

Mixed models for repeated measures (MMRMs) are ubiquitous when analyzing outcomes of clinical trials. However, the linearity of the fixed-effect structure in these models largely restrict their use to estimating treatment effects that are defined as linear combinations of effects on the outcome scale. In some situations, alternative quantifications of treatment effects may be more appropriate. In progressive diseases, for example, one may want to estimate if a drug has cumulative effects resulting in increasing efficacy over time or whether it slows the time progression of disease. This article introduces a class of nonlinear mixed-effects models called progression models for repeated measures (PMRMs) that, based on a continuous-time... (More)

Mixed models for repeated measures (MMRMs) are ubiquitous when analyzing outcomes of clinical trials. However, the linearity of the fixed-effect structure in these models largely restrict their use to estimating treatment effects that are defined as linear combinations of effects on the outcome scale. In some situations, alternative quantifications of treatment effects may be more appropriate. In progressive diseases, for example, one may want to estimate if a drug has cumulative effects resulting in increasing efficacy over time or whether it slows the time progression of disease. This article introduces a class of nonlinear mixed-effects models called progression models for repeated measures (PMRMs) that, based on a continuous-time extension of the categorical-time parametrization of MMRMs, enables estimation of novel types of treatment effects, including measures of slowing or delay of the time progression of disease. Compared to conventional estimates of treatment effects where the unit matches that of the outcome scale (eg, 2 points benefit on a cognitive scale), the time-based treatment effects can offer better interpretability and clinical meaningfulness (eg, 6 months delay in progression of cognitive decline). The PMRM class includes conventionally used MMRMs and related models for longitudinal data analysis, as well as variants of previously proposed disease progression models as special cases. The potential of the PMRM framework is illustrated using both simulated and historical data from clinical trials in Alzheimer's disease with different types of artificially simulated treatment effects. Compared to conventional models it is shown that PMRMs can offer substantially increased power to detect disease-modifying treatment effects where the benefit is increasing with treatment duration.

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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Alzheimer's disease, disease progression model, disease-modifying treatment effects, mixed model for repeated measures, mixed-effects model
in
Statistics in Medicine
volume
41
issue
28
pages
21 pages
publisher
John Wiley & Sons Inc.
external identifiers
  • pmid:36114798
  • scopus:85138273435
ISSN
0277-6715
DOI
10.1002/sim.9581
language
English
LU publication?
yes
id
3ecc9c87-1b9e-430a-8bc8-48cbf741d6dc
date added to LUP
2022-12-05 11:41:38
date last changed
2024-04-18 16:33:54
@article{3ecc9c87-1b9e-430a-8bc8-48cbf741d6dc,
  abstract     = {{<p>Mixed models for repeated measures (MMRMs) are ubiquitous when analyzing outcomes of clinical trials. However, the linearity of the fixed-effect structure in these models largely restrict their use to estimating treatment effects that are defined as linear combinations of effects on the outcome scale. In some situations, alternative quantifications of treatment effects may be more appropriate. In progressive diseases, for example, one may want to estimate if a drug has cumulative effects resulting in increasing efficacy over time or whether it slows the time progression of disease. This article introduces a class of nonlinear mixed-effects models called progression models for repeated measures (PMRMs) that, based on a continuous-time extension of the categorical-time parametrization of MMRMs, enables estimation of novel types of treatment effects, including measures of slowing or delay of the time progression of disease. Compared to conventional estimates of treatment effects where the unit matches that of the outcome scale (eg, 2 points benefit on a cognitive scale), the time-based treatment effects can offer better interpretability and clinical meaningfulness (eg, 6 months delay in progression of cognitive decline). The PMRM class includes conventionally used MMRMs and related models for longitudinal data analysis, as well as variants of previously proposed disease progression models as special cases. The potential of the PMRM framework is illustrated using both simulated and historical data from clinical trials in Alzheimer's disease with different types of artificially simulated treatment effects. Compared to conventional models it is shown that PMRMs can offer substantially increased power to detect disease-modifying treatment effects where the benefit is increasing with treatment duration.</p>}},
  author       = {{Raket, Lars Lau}},
  issn         = {{0277-6715}},
  keywords     = {{Alzheimer's disease; disease progression model; disease-modifying treatment effects; mixed model for repeated measures; mixed-effects model}},
  language     = {{eng}},
  month        = {{12}},
  number       = {{28}},
  pages        = {{5537--5557}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Statistics in Medicine}},
  title        = {{Progression models for repeated measures : Estimating novel treatment effects in progressive diseases}},
  url          = {{http://dx.doi.org/10.1002/sim.9581}},
  doi          = {{10.1002/sim.9581}},
  volume       = {{41}},
  year         = {{2022}},
}