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Main Authors: Tejedor, Guillaume, Peralta, Veronika, Labroche, Nicolas, Marcel, Patrick, Blasco, Hélène, Alarcan, Hugo
Format: Preprint
Published: 2025
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Online Access:https://arxiv.org/abs/2511.01945
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author Tejedor, Guillaume
Peralta, Veronika
Labroche, Nicolas
Marcel, Patrick
Blasco, Hélène
Alarcan, Hugo
author_facet Tejedor, Guillaume
Peralta, Veronika
Labroche, Nicolas
Marcel, Patrick
Blasco, Hélène
Alarcan, Hugo
contents Amyotrophic lateral sclerosis (ALS) is a severe disease with a typical survival of 3-5 years after symptom onset. Current treatments offer only limited life extension, and the variability in patient responses highlights the need for personalized care. However, research is hindered by small, heterogeneous cohorts, sparse longitudinal data, and the lack of a clear definition for clinically meaningful patient clusters. Existing clustering methods remain limited in both scope and number. To address this, we propose a clustering approach that groups sequences using a disease progression declarative score. Our approach integrates medical expertise through multiple descriptive variables, investigating several distance measures combining such variables, both by reusing off-the-shelf distances and employing a weak-supervised learning method. We pair these distances with clustering methods and benchmark them against state-of-the-art techniques. The evaluation of our approach on a dataset of 353 ALS patients from the University Hospital of Tours, shows that our method outperforms state-of-the-art methods in survival analysis while achieving comparable silhouette scores. In addition, the learned distances enhance the relevance and interpretability of results for medical experts.
format Preprint
id arxiv_https___arxiv_org_abs_2511_01945
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Learning a Distance for the Clustering of Patients with Amyotrophic Lateral Sclerosis
Tejedor, Guillaume
Peralta, Veronika
Labroche, Nicolas
Marcel, Patrick
Blasco, Hélène
Alarcan, Hugo
Machine Learning
Amyotrophic lateral sclerosis (ALS) is a severe disease with a typical survival of 3-5 years after symptom onset. Current treatments offer only limited life extension, and the variability in patient responses highlights the need for personalized care. However, research is hindered by small, heterogeneous cohorts, sparse longitudinal data, and the lack of a clear definition for clinically meaningful patient clusters. Existing clustering methods remain limited in both scope and number. To address this, we propose a clustering approach that groups sequences using a disease progression declarative score. Our approach integrates medical expertise through multiple descriptive variables, investigating several distance measures combining such variables, both by reusing off-the-shelf distances and employing a weak-supervised learning method. We pair these distances with clustering methods and benchmark them against state-of-the-art techniques. The evaluation of our approach on a dataset of 353 ALS patients from the University Hospital of Tours, shows that our method outperforms state-of-the-art methods in survival analysis while achieving comparable silhouette scores. In addition, the learned distances enhance the relevance and interpretability of results for medical experts.
title Learning a Distance for the Clustering of Patients with Amyotrophic Lateral Sclerosis
topic Machine Learning
url https://arxiv.org/abs/2511.01945