Evidence map›Paper›PMID 38619747›Full record

ArticleActa neurologica Belgica2024

Long-term follow up of alemtuzumab-treated patients: a retrospective study in a Belgian tertiary care center.

Vincent van Pesch, Andreea-Raluca Hanganu, Souraya El Sankari

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Article in Acta neurologica Belgica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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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.

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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

1 citing paper in PubMed.

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4 · The record

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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

3 authors.

Vincent van PeschDepartment of Neurology, Cliniques Universitaires Saint-Luc (Neurology), UCLouvain, Brussels, Belgium. Vincent.vanpesch@saintluc.uclouvain.be.ORCID http://orcid.org/0000-0003-2885-9004
Andreea-Raluca HanganuCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Souraya El SankariDepartment of Neurology, Cliniques Universitaires Saint-Luc (Neurology), UCLouvain, Brussels, Belgium.ORCID http://orcid.org/0000-0001-5082-1243

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPivotal studies have reported a significant proportion of patients achieving no evidence of disease activity (NEDA) after 2 cycles of treatment with alemtuzumab (ATZ), that can be maintained for several years. Long-term real-world evidence regarding ATZ as well as subsequent treatment trajectories is still scarce.

objectiveTo analyze the effectiveness and safety of ATZ-treated patients in a tertiary care Belgian center.

methodsA retrospective cohort study including 32 patients treated with ATZ between 2015 and 2021 was performed.

results32 patients received 2 ATZ courses with a mean follow-up (FU) duration of 5.6 years (range: 2.25-8.2). 21.75% patients were treatment naïve. 40.5% were previously treated with natalizumab or fingolimod. NEDA-3 was achieved in 61.3-85% of patients, with failure mostly attributed to recurrence of radiological disease activity. During FU, annualized relapse rates remained very low (0.06-0.14), disability improvement occurred in up to 40.5%, whereas disability worsening occurred in up to 13.5%. Retreatment risk was associated with younger age (< 45 years old, Odds Ratio 8.0, p = 0.02) and a higher number of previous DMTs (Hazard ratio 2.7, 95%CI 1.3-7.4, p = 0.02). Safety in our cohort was consistent with the known profile of ATZ. At the end of FU, 65.6% patients remained untreated after 2 or 3 courses of ATZ, while the remaining switched to anti-CD20 therapy or cladribine.

conclusionATZ is a high efficacy therapy for active MS, providing long-term remission in a significant proportion of patients. Retreatment was more frequent in younger patients or patients having failed a higher number of previous DMTs.

Indexed as

AlemtuzumabTertiary Care CentersAdultBelgiumFemaleFollow-Up StudiesHumansImmunologic FactorsMaleMiddle AgedMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingRetrospective StudiesTreatment OutcomeAlemtuzumabImmunologic FactorsAlemtuzumabEffectivenessLong-termMultiple sclerosisReal-world evidenceSafety

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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.