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Baseline Demographics and Disease Characteristics of Patients with Hypereosinophilic Syndrome in a Placebo-Controlled Trial Evaluating the Steroid-Sparing Effects of the Anti-IL-5 Monoclonal Antibody, Mepolizumab.

2006· article· en· W2561500062 on OpenAlexaff
Gerald J. Gleich, Lawrence B. Schwartz, William W. Busse, Johannes Huss‐Marp, Scott R. Walsh

Bibliographic record

VenueBlood · 2006
Typearticle
Languageen
FieldMedicine
TopicEosinophilic Disorders and Syndromes
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsMepolizumabMedicineHypereosinophilic syndromePrednisoneInternal medicinePopulationEosinophiliaClinical endpointEosinophilPlaceboGastroenterologyImmunologyClinical trialAsthmaPathology

Abstract

fetched live from OpenAlex

Abstract Mepolizumab is a humanized anti-IL-5 monoclonal antibody that blocks the actions of IL-5, the hematopoietin most responsible for eosinophil production, differentiation, and survival. Clinical experience in small numbers of patients with hypereosinophilic syndrome (HES), asthma, and atopic dermatitis indicated that intravenous (IV) mepolizumab therapy was associated with a reduction in blood eosinophils and was well-tolerated. A multicenter (26 sites worldwide), randomized, double-blind, placebo-controlled, and parallel-group trial has been conducted to evaluate the steroid-sparing effects of mepolizumab in patients with HES, and its efficacy and safety in controlling the signs and symptoms of this disease. The trial recruited patients 18–85 years of age with HES (blood eosinophil count >1500/μl for ≥6 months with evidence of eosinophilia-related organ involvement or dysfunction, without any known cause of eosinophilia), who tested negative for the FIP1L1-PDGFRα gene rearrangement and required 20–60 mg/day prednisone (monotherapy) to maintain blood eosinophils at <1000 cells/μL during a stabilization period of up to 6 weeks. The primary endpoint was the proportion of patients with disease control on ≤ 10 mg/day prednisone for ≥8 consecutive weeks during the 36-week treatment period. Here we report the baseline demographic and clinical characteristics of trial participants who comprise the largest HES population without the FIP1L1-PDGFRα mutation evaluated to date. Moreover, the clinical spectrum of HES in this population encompassed the multiple varieties of HES currently recognized. Of 107 patients screened, 85 were enrolled, 43 were randomized to mepolizumab (750 mg IV every 4 weeks), and 42 to placebo (saline IV every 4 weeks). No major differences in demographic and disease characteristics were observed between the treatment groups (Table). Many patients (60%) had previously tried and discontinued an HES therapy, notably imatinib mesylate (38%), interferon-α (21%), or hydroxyurea (21%). The most prevalent HES-related medical conditions at baseline were skin (47%) and respiratory (41%) disorders. The primary endpoint was significant in favor of mepolizumab treatment, thus providing evidence that this agent will offer clinical benefits in terms of steroid reduction/sparing in HES. Patient demographics Placebo (n=42) Mepolizumab (n=43) Total (n=85) Age, y (mean±SD) 49.1±14.4 47.0±16.2 48.1±15.3 Men, % 17 (40%) 26 (60%) 43 (51%) Caucasian, % 34 (81%) 38 (88%) 72 (85%) Weight, kg (mean±SD) 79.7±18.3 80.9±22.2 80.3±20.3 BMI, kg/m2 (mean±SD) 27.8±5.8 27.0±6.4 27.4±6.1 Baseline prednisone≤30 mg, n (%) 30 (71%) 30 (70%) 60 (71%) Baseline prednisone >30 mg, n (%) 12 (29%) 13 (30%) 25 (29%) Previously treated for HES, n (%) 40 (95%) 41 (95%) 81 (95%) HES duration, y (mean±SD) 6.5±9.5 4.3±5.6 5.4±7.8 Age at HES onset, y (mean±SD) 42.7±16.2 42.7±17.7 42.7±16.9

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.175
Threshold uncertainty score0.513

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.007
GPT teacher head0.243
Teacher spread0.235 · 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 teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
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".

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Citations0
Published2006
Admission routes1
Has abstractyes

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