We propose a method for recruiting asymptomatic Amyloid positive individuals in clinical trials, using a two-step process. We first select during a pre-screening phase a subset of individuals which are more likely to be amyloid positive based on the automatic analysis of data acquired during routine clinical practice, before doing a confirmatory PET-scan to these selected individuals only. This method leads to an increased number of recruitments and to a reduced number of PETscans, resulting in a decrease in overall recruitment costs. We validate our method on three different cohorts, and consider five different classification algorithms for the pre-screening phase. We show that the best results are obtained using solely cognitive, genetic and socio-demographic features, as the slight increased performance when using MRI or longitudinal data is balanced by the cost increase they induce.We show that the proposed method generalizes well when tested on an independent cohort, and that the characteristics of the selected set of individuals are identical to the characteristics of a population selected in a standard way. The proposed approach shows how Machine Learning can be used effectively in practice to optimize recruitment costs in clinical trials.
Publication
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Année de publication : 2019
Type :
Article de journal
Article de journal
Auteurs :
Ansart, M.
Epelbaum, S.
Gagliardi, G.
Colliot, O.
Dormont, D.
Dubois, B.
Hampel, H.
& Durrleman, S.
for the Alzheimer’s Disease Neuroimaging Initiative* and the INSIGHT-preAD study
Ansart, M.
Epelbaum, S.
Gagliardi, G.
Colliot, O.
Dormont, D.
Dubois, B.
Hampel, H.
& Durrleman, S.
for the Alzheimer’s Disease Neuroimaging Initiative* and the INSIGHT-preAD study
Titre du journal :
Statistical Methods in Medical Research
Statistical Methods in Medical Research
Mots-clés :
pre-screening for clinical trials, recruitment costs, amyloidosis, Alzheimer’s disease, classification, longitudinal data, Random Forest
pre-screening for clinical trials, recruitment costs, amyloidosis, Alzheimer’s disease, classification, longitudinal data, Random Forest