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Durable Effect of Alemtuzumab on Clinical Outcomes in Treatment-Naive Relapsing-Remitting Multiple Sclerosis Patients: Four-Year Follow-up of CARE-MS I (S4.007)

2015· article· en· W903037194 on OpenAlexaff
Alastair Compston, Gavin Giovannoni, Douglas L. Arnold, Edward Fox, Hans‐Peter Hartung, Eva Havrdová, Krzysztof Selmaj, David Margolin, Jeffrey Palmer, Michael Panzara, Alasdair Coles

Bibliographic record

VenueNeurology · 2015
Typearticle
Languageen
FieldMedicine
TopicMultiple Sclerosis Research Studies
Canadian institutionsNeuroRx Research (Canada)Montreal Neurological Institute and Hospital
Fundersnot available
KeywordsAlemtuzumabMultiple sclerosisRelapsing remittingMedicineDimethyl fumarateInternal medicineOncologyImmunology

Abstract

fetched live from OpenAlex

OBJECTIVE: Examine alemtuzumab’s 4-year efficacy and safety in the CARE-MS I extension study. BACKGROUND: In the 2-year core study, alemtuzumab had superior effect on relapse versus subcutaneous interferon beta-1a with manageable tolerability and safety in treatment-naive relapsing-remitting multiple sclerosis (RRMS) patients. Alemtuzumab’s efficacy was subsequently shown to be durable through 3 years. DESIGN/METHODS: In CARE-MS I (NCT00530348), patients received alemtuzumab 12 mg at baseline and month 12. In extension (NCT00930553), alemtuzumab-treated patients received as-needed alemtuzumab retreatments 蠅1 year apart. Endpoints included annualized relapse rate (ARR), improved/stable/worsened Expanded Disability Status Scale (EDSS) score (蠅0.5-point decrease [improvement] or 蠅0.5-point increase [worsening] from core baseline), sustained accumulation of disability (SAD; 蠅1-point EDSS increase over 蠅6 months [蠅1.5-point if baseline EDSS=0]), and sustained reduction in preexisting disability (SRD; 蠅1-point EDSS decrease from baseline over 蠅6 months [patients with baseline score 蠅2.0]). RESULTS: The extension study enrolled 349 (95[percnt]) CARE-MS I alemtuzumab-treated patients. Through 4 years, 73[percnt] received only the initial 2 treatment courses; 21[percnt] received 1 additional course, and 5[percnt] received 2 additional courses. ARR was maintained from Year 3 (0.19) to Year 4 (0.14). From baseline to end of Year 4: 73[percnt] of patients had stable or improved EDSS scores; 83[percnt] of patients did not experience 6-month SAD; and 30[percnt] of patients achieved 6-month SRD. Incidence of infusion-associated reactions and infections were greatest after first course. Thyroid adverse event incidence peaked at Year 3 and subsequently declined. CONCLUSIONS: Alemtuzumab’s efficacy was maintained over 4 years despite most patients not having received additional treatment over the previous 3 years. The safety profile during the extension study was consistent with the core study; no unexpected adverse events occurred. These findings support the durable efficacy and favorable benefit-risk profile of alemtuzumab in treatment-naive RRMS patients. Study Supported by: Genzyme, a Sanofi company, and Bayer Healthcare Pharmaceuticals

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.004
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Non-randomized trial · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.019

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0040.003
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.000
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.106
GPT teacher head0.355
Teacher spread0.249 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNon-randomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations5
Published2015
Admission routes1
Has abstractyes

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