Evidence map›Paper›PMID 30967831›Full record

ReviewFrontiers in neurology2019

Best Practices for Long-Term Monitoring and Follow-Up of Alemtuzumab-Treated MS Patients in Real-World Clinical Settings.

Krista Barclay, Robert Carruthers, Anthony Traboulsee, Ann D Bass, Christopher LaGanke, Antonio Bertolotto, Aaron Boster, Elisabeth G Celius, Jérôme de Seze, Dionisio Dela Cruz and 10 more

4 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Frontiers in neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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.

NCT00530348 phase3completednot on this map

A Phase 3 Randomized, Rater-Blinded Study Comparing Two Annual Cycles of Intravenous Alemtuzumab to Three-Times Weekly Subcutaneous Interferon Beta-1a (Rebif®) in Treatment-Naïve Patients With Relapsing-Remitting Multiple Sclerosis

TypeinterventionalSponsorGenzyme, a Sanofi CompanyRan2007 to 2011Enrolled581ConditionsMultiple Sclerosis, Relapsing-RemittingArmsAlemtuzumab, Interferon beta-1a
NCT00548405 phase3completednot on this map

A Phase 3, Randomized, Rater- and Dose-Blinded Study Comparing Two Annual Cycles of Intravenous Low- and High-Dose Alemtuzumab to Three-Times Weekly Subcutaneous Interferon Beta 1a (Rebif®) in Patients With Relapsing Remitting Multiple Sclerosis Who Have Relapsed On Therapy

TypeinterventionalSponsorGenzyme, a Sanofi CompanyRan2007 to 2011Enrolled840ConditionsMultiple Sclerosis, Relapsing-RemittingArmsAlemtuzumab 12 mg, Alemtuzumab 24 mg, Interferon beta-1a
NCT00930553 phase3completednot on this map

An Extension Protocol for Multiple Sclerosis Patients Who Participated in Genzyme-Sponsored Studies of Alemtuzumab

TypeinterventionalSponsorGenzyme, a Sanofi CompanyRan2009 to 2016Enrolled1,314ConditionsMultiple Sclerosis, Relapsing-RemittingArmsalemtuzumab
NCT02255656 phase4completednot on this map

A Long-term Follow-up Study for Multiple Sclerosis Patients Who Have Completed the Alemtuzumab Extension Study (CAMMS03409)

TypeinterventionalSponsorGenzyme, a Sanofi CompanyRan2015 to 2020Enrolled1,062ConditionsRelapsing Remitting Multiple SclerosisArmsalemtuzumab GZ402673
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 22 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

20 authors at 18 institutions in 10 countries.

Krista BarclayVancouver Coastal Health, Vancouver, BC, Canada.
Robert CarruthersUniversity of British Columbia, Vancouver, BC, Canada.
Anthony TraboulseeUniversity of British Columbia, Vancouver, BC, Canada.
Ann D BassNeurology Center of San Antonio, San Antonio, TX, United States.
Christopher LaGankeNorth Central Neurology Associates, Cullman, AL, United States.
Antonio BertolottoAzienda Ospedaliero Universitaria San Luigi, Orbassano, Italy.
Aaron BosterOhioHealth Neurological Physicians, Columbus, OH, United States.
Elisabeth G CeliusOslo University Hospital Ullevål and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Jérôme de SezeClinical Research Center (CIC), INSERM 1434, Strasbourg University, Strasbourg, France.
Dionisio Dela CruzImperial College Healthcare NHS Trust, London, United Kingdom.
Mario HabekUniversity of Zagreb, School of Medicine and University Medical Center, Zagreb, Croatia.
Jong-Mi LeeStanford Healthcare, Palo Alto, CA, United States.
Volker LimmrothKlinik für Neurologie und Palliativmedizin, Cologne, Germany.
Sven G MeuthClinic of Neurology with Institute of Translational Neurology, University Hospital Müenster, Müenster, Germany.
Celia Oreja-GuevaraEl Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Hospital Clínico San Carlos, Madrid, Spain.
Patricia PagnottaNeurology Associates, Maitland, FL, United States.
Cindy VosRevalidatie & MS Centrum, Overpelt, Belgium.
Tjalf ZiemssenCenter of Clinical Neuroscience, University Clinic Carl Gustav Carus, Dresden, Germany.
Darren P BakerSanofi, Cambridge, MA, United States.
Bart Van WijmeerschRehabilitation & MS-Centre Overpelt, Hasselt University, Hasselt, Belgium.
University of British Columbia · CAHasselt University · BEImperial College Healthcare NHS Trust · GBInserm · FRInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESKlinik und Poliklinik für Neurologie · DENeurology Associates · USOhioHealth · USOslo University Hospital · NOOspedale San Luigi Gonzaga · ITSanofi (United States) · USStanford Health Care · USUniversity Hospital Carl Gustav Carus · DEUniversity Hospital Münster · DEUniversity of Zagreb · HRUrology Associates · USUrology San Antonio · USVancouver Coastal Health · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is a chronic autoimmune neurological disease that typically affects young adults, causing irreversible physical disability and cognitive impairment. Alemtuzumab, administered intravenously as 2 initial courses of 12 mg/day (5 consecutive days at baseline, and 3 consecutive days 12 months later), resulted in significantly greater improvements in clinical and MRI outcomes vs. subcutaneous interferon beta-1a over 2 years in patients with active relapsing-remitting MS (RRMS) who were either treatment-naive (CARE-MS I; NCT00530348) or had an inadequate response to prior therapy (CARE-MS II; NCT00548405). Efficacy with alemtuzumab was maintained over 7 years in subsequent extension studies (NCT00930553; NCT02255656), in the absence of continuous treatment and with a consistent safety profile. There is an increased incidence of autoimmune events in patients treated with alemtuzumab (mainly thyroid events, but also immune thrombocytopenia and nephropathy), which imparts a need for mandatory safety monitoring for 4 years following the last treatment. The risk management strategy for alemtuzumab-treated patients includes laboratory monitoring and a comprehensive patient education and support program that enables early detection and effective management of autoimmune events, yielding optimal outcomes for MS patients. Here we provide an overview of tools and techniques that have been implemented in real-world clinical settings to reduce the burden of monitoring for both patients and healthcare providers, including customized educational materials, the use of social media, and interactive online databases for managing healthcare data. Many practices are also enhancing patient outreach efforts through coordination with specialized nursing services and ancillary caregivers. The best practice recommendations for safety monitoring described in this article, based on experiences in real-world clinical settings, may enable early detection and management of autoimmune events, and help with implementation of monitoring requirements while maximizing the benefits of alemtuzumab treatment for MS patients.

Indexed as

alemtuzumabanti-CD52 monoclonal antibodyautoimmune eventsbest practicesdisease-modifying therapymonitoringreal-world settingsrelapsing-remitting multiple sclerosis

Identifiers

PMID30967831
PMCPMC6439479
OpenAlexW2923768067

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.