Evidence map›Paper›PMID 30986126›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2019

Incidence, management, and outcomes of autoimmune nephropathies following alemtuzumab treatment in patients with multiple sclerosis.

Richard Phelps, Jonathan A Winston, Daniel Wynn, Mario Habek, Hans-Peter Hartung, Eva Kubala Havrdová, Glen S Markowitz, David H Margolin, Claudio E Rodriguez, Darren P Baker and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

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  13. Emerging safety issues in alemtuzumab-treated MS patients.Multiple sclerosis (Houndmills, Basingstoke, England) · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 5 countries.

Richard PhelpsCentre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Jonathan A WinstonMount Sinai School of Medicine, New York, NY, USA.
Daniel WynnConsultants in Neurology MS Center, Northbrook, IL, USA.
Mario HabekDepartment of Neurology, School of Medicine, University of Zagreb and University Hospital Center, Zagreb, Croatia.ORCID 0000-0002-3360-1748
Hans-Peter HartungDepartment of Neurology, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.
Eva Kubala HavrdováDepartment of Neurology, First Medical Faculty, Charles University, Prague, Czech Republic.
Glen S MarkowitzDepartment of Pathology and Cell Biology, Columbia University, New York, NY, USA.
David H MargolinSanofi, Cambridge, MA, USA/Cerevance Inc., Boston, MA, USA.
Claudio E RodriguezSanofi, Cambridge, MA, USA/Sunovion Pharmaceuticals, Marlborough, MA, USA.
Darren P BakerSanofi, Cambridge, MA, USA.
Alasdair J ColesSchool of Medicine, University of Cambridge, Cambridge, UK.
Sanofi (United States) · USCentre for Inflammation Research · GBCharles University · CZColumbia University · USConsultants in Neurology · USHeinrich Heine University Düsseldorf · DEIcahn School of Medicine at Mount Sinai · USUniversity Hospital Centre Zagreb · HRUniversity of Cambridge · GB

Funding

Medical Research Council G1100114
6 · The paper itself

Abstract

backgroundAutoimmune disorders including nephropathies have been reported more frequently in alemtuzumab-treated multiple sclerosis (MS) patients than in the general population.

objectiveDescribe instances of autoimmune nephropathy in alemtuzumab-treated MS patients.

methodsCases were identified from safety monitoring within the alemtuzumab relapsing-remitting multiple sclerosis (RRMS) clinical development program (CDP) or post-marketing, or following off-label use.

resultsAs of 16 June 2017, 16 autoimmune nephropathies have occurred following alemtuzumab treatment for MS. The incidence of autoimmune nephropathies was 0.34% within the CDP (5/1485 patients). The five CDP cases (one of anti-glomerular basement membrane (anti-GBM) disease, two of membranous glomerulonephropathy, and two of serum anti-GBM antibody without typical anti-GBM disease) were identified early, responded to conventional therapy (where needed), and had favorable outcomes. Three of 11 cases outside the CDP occurred following off-label alemtuzumab use prior to approval for RRMS and were all anti-GBM disease. Diagnosis was delayed in one of these three cases and another did not receive appropriate treatment; all three cases resulted in end-stage renal failure. All anti-GBM disease cases with documented urinalysis demonstrated prior microscopic hematuria.

conclusionClose monitoring of alemtuzumab-treated MS patients facilitates diagnosis and treatment early in the nephropathy course when preservation of renal function is more likely.

Indexed as

AdultAlemtuzumabFemaleFollow-Up StudiesGlomerulonephritisGlomerulonephritis, MembranousHemorrhageHumansImmunologic FactorsIncidenceLung DiseasesMaleMultiple Sclerosis, Relapsing-RemittingAlemtuzumabImmunologic FactorsAlemtuzumabanti-glomerular basement membrane diseasedisease-modifying therapymembranous glomerulonephropathymultiple sclerosisnephropathy

Identifiers

PMID30986126
PMCPMC6681440
OpenAlexW2938804432

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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.