Reliability of Outcome Measures in Clinical Trials in Secondary Progressive Multiple Sclerosis.
Adult
Datasets as Topic
Disability Evaluation
Female
Humans
Immunologic Factors
/ therapeutic use
Interferon beta-1a
/ therapeutic use
Male
Middle Aged
Multiple Sclerosis, Chronic Progressive
/ drug therapy
Natalizumab
/ therapeutic use
Outcome Assessment, Health Care
/ standards
Randomized Controlled Trials as Topic
Reproducibility of Results
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
05 01 2021
05 01 2021
Historique:
received:
14
02
2020
accepted:
06
08
2020
pubmed:
28
10
2020
medline:
16
1
2021
entrez:
27
10
2020
Statut:
ppublish
Résumé
To investigate the reliability of clinical outcomes in secondary progressive multiple sclerosis (SPMS) trials, we compared the frequency of progression and improvement events on different clinical outcome measures in the placebo arms of 2 large randomized controlled trial (RCT) datasets. Using original trial data from the placebo arms of IMPACT (International MS Secondary Progressive Avonex Controlled Trial) and ASCEND (A Clinical Study of the Efficacy of Natalizumab on Reducing Disability Progression in Participants With Secondary Progressive Multiple Sclerosis), 2 large RCTs in SPMS, we compared disability progression and similarly defined improvement with and without 3- or 6-month confirmation on the outcome measures Expanded Disability Status Scale (EDSS), Timed 25-Foot Walk (T25FW), 9-Hole Peg Test (9HPT), and their combinations. In both datasets, the EDSS showed the highest rates of improvement over time, and the smallest difference between progression and improvement rates, followed by the T25FW and the 9HPT. For the T25FW and 9HPT, improvement rates were fairly stable over time and remained at below or around the 10% level. For the EDSS, improvement rates increased in parallel with disability progression rates. All investigated outcome measures in SPMS showed some evidence of random variation and measurement error, the T25FW and 9HPT less so than the more established outcome EDSS. Our findings are relevant for the design and critical appraisal of trials in SPMS.
Identifiants
pubmed: 33106389
pii: WNL.0000000000011123
doi: 10.1212/WNL.0000000000011123
doi:
Substances chimiques
Immunologic Factors
0
Natalizumab
0
Interferon beta-1a
XRO4566Q4R
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e111-e120Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2020 American Academy of Neurology.