Evidence map›Paper›PMID 36064841›Full record

ArticleCNS drugs2022

Improvements in Cognitive Processing Speed, Disability, and Patient-Reported Outcomes in Patients with Early Relapsing-Remitting Multiple Sclerosis Treated with Natalizumab: Results of a 4-year, Real-World, Open-Label Study.

Jai Perumal, Roumen Balabanov, Ray Su, Roger Chang, Laura J Balcer, Steven L Galetta, Robin L Avila, Danette Rutledge, Robert J Fox

Erratum issued Registry-linked trialOpen access · hybridAbstract readMulticenter Study
In one paragraph

Article in CNS drugs, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT01485003 (A Multicenter, Observational, Open-Label, Single-Arm Study of Tysabri in Early Relapsing-Remitting Multiple Sclerosis in Anti-JCV Antibody Negative Patients), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01485003 completednot on this map

A Multicenter, Observational, Open-Label, Single-Arm Study of Tysabri in Early Relapsing-Remitting Multiple Sclerosis in Anti-JCV Antibody Negative Patients

TypeobservationalSponsorBiogenRan2012 to 2018Enrolled231ConditionsRelapsing-Remitting Multiple SclerosisArmsnatalizumab
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  5. Real-world evidence and patient preference for subcutaneousTherapeutic advances in neurological disorders · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Jai PerumalWeill Cornell Medical College, Cornell University, 1305 York Ave #2F, New York, NY, 10065, USA. jaisperumal@gmail.com.
Roumen BalabanovNorthwestern University, Chicago, IL, USA.
Ray SuBiogen, Cambridge, MA, USA.
Roger ChangBiogen, Cambridge, MA, USA.
Laura J BalcerNew York University Grossman School of Medicine, New York, NY, USA.
Steven L GalettaNew York University Grossman School of Medicine, New York, NY, USA.
Robin L AvilaBiogen, Cambridge, MA, USA.
Danette RutledgeBiogen, Cambridge, MA, USA.
Robert J FoxMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, USA.
Biogen (United States) · USNew York University · USCleveland Clinic · USCornell University · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSTRIVE was a prospective, 4-year, multicenter, observational, open-label, single-arm study of natalizumab treatment in anti-JC virus antibody-negative patients with early relapsing-remitting multiple sclerosis (RRMS).

objectiveStudy objectives examined the effects of natalizumab on cognitive processing speed, confirmed disability improvement (CDI), and patient-reported outcomes (PROs).

methodsClinical and PRO secondary endpoints were assessed annually over 4 years in STRIVE. The Symbol Digit Modalities Test (SDMT) was used as a measure of cognitive processing speed. PROs were assessed using the Multiple Sclerosis Impact Score (MSIS-29) and the Work Productivity and Activity Impairment Questionnaire (WPAI).

resultsAt all four annual assessments, the proportion of patients in the intent-to-treat (ITT) population (N = 222) who exhibited clinically meaningful improvement in their SDMT score from baseline (i.e., change ≥ 4 points) ranged from 41.9 to 54.0%. The cumulative probability of CDI at 4 years in patients in the ITT population with a baseline Expanded Disability Status Scale score ≥ 2 (N = 133) was 43.9%. Statistically significant reductions in the mean change from screening in the MSIS-29 physical and psychological scores, indicating improved quality of life, were observed over all 4 years (P ≤ 0.0012 for all). A statistically significant decrease from screening in the impact of MS on regular activities, signifying an improvement in this WPAI measure, was also observed over all 4 years of the study.

conclusionThese results further extend our knowledge of the effectiveness, specifically regarding improvements in cognitive processing speed, disability and PROs, of long-term natalizumab treatment in early RRMS patients. CLINICALTRIALS: GOV: NCT01485003 (5 December 2011).

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingCognitionHumansImmunologic FactorsNatalizumabPatient Reported Outcome MeasuresProspective StudiesQuality of LifeImmunologic FactorsNatalizumab

Identifiers

PMID36064841
PMCPMC9797458
OpenAlexW4294631535

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.