Evidence map›Paper›PMID 35672926›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2022

Ocrelizumab reduces thalamic volume loss in patients with RMS and PPMS.

Douglas L Arnold, Till Sprenger, Amit Bar-Or, Jerry S Wolinsky, Ludwig Kappos, Shannon Kolind, Ulrike Bonati, Stefano Magon, Johan van Beek, Harold Koendgen and 4 more

3 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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.

NCT01194570 phase3completednot on this map

A Phase III, Multicentre, Randomized, Parallel-group, Double-blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Ocrelizumab in Adults With Primary Progressive Multiple Sclerosis

TypeinterventionalSponsorHoffmann-La RocheRan2011 to 2022Enrolled735ConditionsMultiple Sclerosis, Primary ProgressiveArmsOcrelizumab, Placebo
NCT01247324 phase3completednot on this map

A Randomized, Double-Blind, Double-Dummy, Parallel-Group Study To Evaluate the Efficacy and Safety of Ocrelizumab in Comparison to Interferon Beta-1a (Rebif®) in Patients With Relapsing Multiple Sclerosis

TypeinterventionalSponsorHoffmann-La RocheRan2011 to 2022Enrolled821ConditionsRelapsing Multiple SclerosisArmsInterferon beta-1a, Ocrelizumab-matching placebo, Ocrelizumab, Interferon beta-1a-matching placebo
NCT01412333 phase3completednot on this map

A Randomized, Double-Blind, Double-Dummy, Parallel-Group Study To Evaluate the Efficacy and Safety of Ocrelizumab in Comparison to Interferon Beta-1a (Rebif) in Patients With Relapsing Multiple Sclerosis

TypeinterventionalSponsorHoffmann-La RocheRan2011 to 2022Enrolled835ConditionsRelapsing Multiple SclerosisArmsInterferon beta-1a, Ocrelizumab-matching placebo, Ocrelizumab, Interferon beta-1a-matching placebo
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. The effect of ibudilast on thalamic volume in progressive multiple sclerosis.Multiple sclerosis (Houndmills, Basingstoke, England) · 2023
    Trial
  4. Trial
  5. Article
  6. Article
  7. Observational
  8. Decoding Gray Matter Involvement in Multiple Sclerosis via Imaging.Neuroimaging clinics of North America · 2024
    Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

Douglas L ArnoldMontreal Neurological Institute, McGill University, Montreal, QC, Canada/NeuroRx Research, Montreal, QC, Canada.ORCID 0000-0003-4266-0106
Till SprengerDepartment of Neurology, DKD Helios Klinik Wiesbaden, Wiesbaden, Germany/Research Center for Clinical Neuroimmunology and Neuroscience and MS Center, Departments of Medicine, Clinical Research and Biomedical Engineering, University Hospital Basel and University of Basel, Basel, Switzerland.
Amit Bar-OrDepartment of Neurology and Center for Neuroinflammation and Experimental Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Jerry S WolinskyMcGovern Medical School, The University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.ORCID 0000-0002-8197-2762
Ludwig KapposResearch Center for Clinical Neuroimmunology and Neuroscience and MS Center, Departments of Medicine, Clinical Research and Biomedical Engineering, University Hospital Basel and University of Basel, Basel, Switzerland.ORCID 0000-0003-4175-5509
Shannon KolindUniversity of British Columbia, Vancouver, BC, Canada.
Ulrike BonatiHoffmann-La Roche Ltd, Basel, Switzerland.
Stefano MagonF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Johan van BeekF. Hoffmann-La Roche Ltd, Basel, Switzerland/Biogen, Baar, Switzerland.
Harold KoendgenF. Hoffmann-La Roche Ltd, Basel, Switzerland/UCB Farchim SA, Bulle, Switzerland.
Oscar BortolamiF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Corrado BernasconiF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Laura GaetanoF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Anthony TraboulseeUniversity of British Columbia, Vancouver, BC, Canada.
Roche (Switzerland) · CHUniversity of Basel · CHUniversity of British Columbia · CANeuroRx Research (Canada) · CAThe University of Texas Health Science Center at Houston · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn multiple sclerosis (MS), thalamic integrity is affected directly by demyelination and neuronal loss, and indirectly by gray/white matter lesions outside the thalamus, altering thalamic neuronal projections.

objectiveTo assess the efficacy of ocrelizumab compared with interferon beta-1a (IFNβ1a)/placebo on thalamic volume loss and the effect of switching to ocrelizumab on volume change in the Phase III trials in relapsing MS (RMS, OPERA I/II; NCT01247324/NCT01412333) and in primary progressive MS (PPMS, ORATORIO; NCT01194570).

methodsThalamic volume change was computed using paired Jacobian integration and analyzed using an adjusted mixed-effects repeated measurement model.

resultsOver the double-blind period, ocrelizumab treatment significantly reduced thalamic volume loss with the largest effect size (Cohen's

conclusionOcrelizumab effectively reduced thalamic volume loss compared with IFNβ1a/placebo. Early treatment effects on thalamic tissue preservation persisted over time. Thalamic volume loss could be a potential sensitive marker of persisting tissue damage.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingAntibodies, Monoclonal, HumanizedClinical Trials, Phase III as TopicDouble-Blind MethodHumansImmunologic FactorsInterferon beta-1aMagnetic Resonance ImagingRandomized Controlled Trials as TopicAntibodies, Monoclonal, HumanizedImmunologic FactorsInterferon beta-1aocrelizumabatrophymultiple sclerosisOcrelizumabthalamustreatment outcome

Identifiers

PMID35672926
PMCPMC9493406
OpenAlexW4281725428

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.