Evidence map›Paper›PMID 31209573›Full record

ArticleJournal of neurology2019

Outcomes after fingolimod to alemtuzumab treatment shift in relapsing-remitting MS patients: a multicentre cohort study.

Jessica Frau, Francesco Saccà, Alessio Signori, Damiano Baroncini, Giuseppe Fenu, Pietro Annovazzi, Marco Capobianco, Elisabetta Signoriello, Alice Laroni, Sara La Gioia and 11 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 20 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

21 authors at 8 institutions in 1 country.

Jessica FrauDepartment of Medical Sciences and Public Health, Multiple Sclerosis Centre, University of Cagliari-ATS Sardegna, Via Is Guadazzonis 2, 09126, Cagliari, Italy. jessicafrauneuro@gmail.com.
Francesco SaccàNSRO Department Federico II University, Naples, Italy.
Alessio SignoriSection of Biostatistics, Department of Health Sciences, University of Genoa, Genoa, Italy.
Damiano BaronciniMultiple Sclerosis Centre, ASST Valle-Olona, Gallarate Hospital, Gallarate, VA, Italy.
Giuseppe FenuDepartment of Medical Sciences and Public Health, Multiple Sclerosis Centre, University of Cagliari-ATS Sardegna, Via Is Guadazzonis 2, 09126, Cagliari, Italy.
Pietro AnnovazziMultiple Sclerosis Centre, ASST Valle-Olona, Gallarate Hospital, Gallarate, VA, Italy.
Marco CapobiancoSCDO Neurologia-Centro di Riferimento Regionale Sclerosi Multipla, AOU San Luigi Gonzaga, Orbassano, TO, Italy.
Elisabetta SignorielloMultiple Sclerosis Centre Second Division of Neurology, University of Campania Luigi Vanvitelli, Naples, Italy.
Alice LaroniDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health and Center of Excellence for Biomedical Research, University of Genova, Genoa, Italy.
Sara La GioiaASST Papa Giovanni XXIII, Bergamo, Italy.
Arianna SartoriAOU Ospedali Riuniti di Trieste, Trieste, Italy.
Giorgia Teresa ManiscalcoNeurology and Stroke Unit, A. Cardarelli Hospital, Naples, Italy.
Simona BonavitaDepartment of Medical, Surgical, Neurological, Metabolic and Aging Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.
Marinella ClericoClinical and Biological Sciences Department, AOU San Luigi Gonzaga University of Turin, Turin, Italy.
Cinzia Valeria RussoNSRO Department Federico II University, Naples, Italy.
Antonio GalloDepartment of Medical, Surgical, Neurological, Metabolic and Aging Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.
Caterina LapucciDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health and Center of Excellence for Biomedical Research, University of Genova, Genoa, Italy.
Antonio CarotenutoNSRO Department Federico II University, Naples, Italy.
Maria Pia SormaniSection of Biostatistics, Department of Health Sciences, University of Genoa, Genoa, Italy.
Eleonora CoccoDepartment of Medical Sciences and Public Health, Multiple Sclerosis Centre, University of Cagliari-ATS Sardegna, Via Is Guadazzonis 2, 09126, Cagliari, Italy.
i-MuST study group
University of Campania "Luigi Vanvitelli" · ITFederico II University Hospital · ITATS Sardegna (Italy) · ITUniversity of Cagliari · ITOspedale Papa Giovanni XXIII · ITAssociazione Italiana Sclerosi Multipla · ITFatebenefratelli Hospital · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA high reactivation of multiple sclerosis (MS) was reported in patients treated with alemtuzumab after fingolimod. We aimed to understand whether this shift enhanced the risk for reactivation in a real-life cohort.

methodsSubjects with relapsing MS, shifting from fingolimod to alemtuzumab were enrolled. We collected the following data: age, sex, disease duration, relapses after fingolimod withdrawal, new T2/gadolinium (Gd)-enhancing lesions in the last magnetic resonance imaging (MRI) during fingolimod and in the first, while on alemtuzumab, lymphocyte counts at alemtuzumab start, and Expanded Disability Status Scale (EDSS) before and after alemtuzumab.

resultsWe enrolled 77 patients (women 61 (79%); mean age 36.2 years (SD 9.6), and disease duration 12.3 years (SD 6.8) at fingolimod discontinuation; median washout 1.8 months). The annualised relapse rate was 0.89 during fingolimod, 1.32 during washout, and 0.15 after alemtuzumab (p = 0.001). The EDSS changed from a median of 3 (IQR 2-4) at the end of fingolimod to 2.5 after alemtuzumab (IQR 1.5-4) (p = 0.013). The washout length and the lymphocyte count before alemtuzumab were not associated with EDSS change after alemtuzumab (p = 0.59 and p = 0.33, respectively). MRI activity decreased after alemtuzumab compared to that during fingolimod (p = 0.001). At alemtuzumab start, lymphocyte counts were < 0.8 × 10

conclusionsIn our cohort, alemtuzumab reduced relapse, new T2/Gd-enhancing lesions, and EDSS score, as compared to the previous periods (fingolimod/washout). These results were not related to washout length or lymphocyte counts. Therefore, a rapid initiation of alemtuzumab after fingolimod does not seem to be a risk factor for MS reactivation.

Indexed as

Outcome Assessment, Health CareAdultAlemtuzumabFemaleFingolimod HydrochlorideHumansImmunologic FactorsMagnetic Resonance ImagingMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingRetrospective StudiesSeverity of Illness IndexAlemtuzumabFingolimod HydrochlorideImmunologic FactorsAlemtuzumabFingolimodNEDAReal life

Identifiers

PMID31209573
OpenAlexW2951170071

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Registered trials

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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.