Prevalence of disability improvement as a potential outcome for multiple sclerosis trials

Author:

Signori Alessio1ORCID,Boffa Giacomo2ORCID,Bovis Francesca1ORCID,Mariottini Alice3,Repice Annamaria4,Inglese Matilde2,Amato Maria Pia5,Mancardi Gianluigi6,Massacesi Luca3,Saccardi Riccardo7,Sormani Maria Pia8ORCID

Affiliation:

1. Department of Health Sciences, University of Genova, Italy

2. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health and Center of Excellence for Biomedical Research (CEBR), University of Genova, Genova, Italy/IRCCS Ospedale Policlinico San Martino, Genova, Italy

3. Department of Neurology 2, Careggi University Hospital, Florence, Italy/Department of Neurosciences, University of Florence, Florence, Italy

4. Department of Neurology 2, Careggi University Hospital, Florence, Italy

5. Department of Neurosciences, University of Florence, Florence, Italy/IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy

6. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health and Center of Excellence for Biomedical Research (CEBR), University of Genova, Genova, Italy

7. Department of Cell Therapy and Transfusional Medicine, Careggi University Hospital, Florence, Italy

8. Department of Health Sciences, University of Genova, Italy/IRCCS Ospedale Policlinico San Martino, Genova, Italy

Abstract

Background: The concept of improvement of disability recently emerged as a new target in multiple sclerosis (MS) studies since the approval of new potent drugs and for testing drugs for neuroprotection and repair. Objective: To propose a simple estimator for assessing and comparing the prevalence of improvement over time between groups. Methods: The prevalence of a transient condition takes into account the incidence and the duration of such condition. We propose here the application of a modified Kaplan–Meier estimator to evaluate and compare between groups the prevalence of improvement over time in a cohort of 121 patients treated with autologous hematopoietic stem cell transplantation. Results: The prevalence of improvement after 5 years from transplant was 50.3% (95%CI: [38.0–63.0]) in relapsing–remitting patients and 6.5% (95%CI: [0–17.8]) in secondary-progressive patients ( p < 0.001). Such a difference wouldn’t be evident considering the traditional cumulative probability of improvement at 5 years (55.5% in relapsing–remitting vs 33.4% in secondary-progressive patients, p = 0.10). Conclusion: This study shows the relevance of a new estimator of prevalence of improvement in MS. This estimator gives simple information on whether a drug can induce a durable improvement in disability and can be considered a potential outcome for trials assessing drugs for neuroprotection or repair.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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