Evidence map›Paper›PMID 27314959›Full record

Trial reportJournal of neurology2016

Subgroup and sensitivity analyses of annualized relapse rate over 2 years in the ADVANCE trial of peginterferon beta-1a in patients with relapsing-remitting multiple sclerosis.

Scott D Newsome, Bernd C Kieseier, Douglas L Arnold, Shulian Shang, Shifang Liu, Serena Hung, Guido Sabatella

Open access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

7 authors at 4 institutions in 3 countries.

Scott D NewsomeDepartment of Neurology, Johns Hopkins University, Baltimore, MD, USA. snewsom2@jhmi.edu.
Bernd C KieseierDepartment of Neurology, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.
Douglas L ArnoldMontreal Neurological Institute, McGill University, Montreal, QC, Canada.
Shulian ShangBiogen, Cambridge, MA, USA.
Shifang LiuBiogen, Cambridge, MA, USA.
Serena HungBiogen, Cambridge, MA, USA.
Guido SabatellaBiogen, Cambridge, MA, USA.
Biogen (United States) · USHeinrich Heine University Düsseldorf · DEJohns Hopkins University · USMontreal Neurological Institute and Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ADVANCE was a 2-year, double-blind, placebo-controlled, Phase 3 study in 1512 patients aged 18-65 years with relapsing-remitting multiple sclerosis, which demonstrated that peginterferon beta-1a 125 mcg administered subcutaneously every 2 or 4 weeks led to significant reductions in annualized relapse rate (ARR) compared with placebo. This analysis examined ARR over 2 years in ADVANCE across subgroups. Patients were treated with peginterferon beta-1a every 2 weeks or every 4 weeks, or placebo during Year 1. Thereafter, patients on placebo were re-randomized to peginterferon beta-1a every 2 weeks or every 4 weeks (delayed treatment). Subgroup analyses were conducted by demographics and baseline disease characteristics. The following results compared ARR in these subgroups for patients in continuous 2-week treatment versus continuous 4-week treatment. ARR was similar in most demographic and baseline disease characteristic subgroups evaluated within the peginterferon beta-1a every-2-week arm or every-4-week arm over 2 years. Although for both doses some differences in the point estimates for ARR were noted among the subgroups, considerable overlap in the confidence intervals suggested that the efficacy of peginterferon beta-1a is similar in all patients irrespective of gender, age, body weight, geographical region, and disease activity at initiation of treatment. Within each peginterferon beta-1a dosing group, ARR was generally similar across most subgroups.

Indexed as

AdolescentAdultAgedDisability EvaluationDouble-Blind MethodFemaleHumansImmunologic FactorsInterferon-betaInternationalityMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingPolyethylene GlycolsRecurrenceSensitivity and SpecificityImmunologic FactorsInterferon-betapeginterferon beta-1aPolyethylene GlycolsClinical trialInterferonMultiple sclerosisPeginterferon beta-1aPegylatedPhase 3Relapsing-remitting

Identifiers

PMID27314959
PMCPMC5010838
OpenAlexW2436980626

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.