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Record W1976199411 · doi:10.1186/ar4659

Outcome measures in systemic lupus erythematosus: constructing a meaningful response index from existing clinical trial data

2014· article· en· W1976199411 on OpenAlexfundno aff
Lindsy Forbess, Daniel J. Wallace, Mariko Ishimori, Michael H. Weisman

Bibliographic record

VenueArthritis Research & Therapy · 2014
Typearticle
Languageen
FieldMedicine
TopicSystemic Lupus Erythematosus Research
Canadian institutionsnot available
FundersNational Institute of Allergy and Infectious DiseasesCanadian Institutes of Health ResearchNational Institutes of HealthLupus Research AllianceCanadian Arthritis NetworkNational Institute of Arthritis and Musculoskeletal and Skin DiseasesArthritis SocietyCentral New York Community FoundationMerck KGaALupus Foundation of America
KeywordsMedicineRheumatologyInternal medicineIndex (typography)Clinical trialOutcome (game theory)Intensive care medicinePhysical therapyComputer science

Abstract

fetched live from OpenAlex

The purpose of this project is to develop a systemic lupus erythematosus (SLE) response index as a standard outcome measure in future therapeutic trials. Currently, there is no widely validated method for defining response to therapy. Most SLE trials to date have failed to meet predesigned endpoints, leading to controversy over whether it is drug treatments or outcome measures that are unsuccessful in SLE. A similar controversy in rheumatoid arthritis (RA) years ago was resolved by examining data from placebo-controlled trials with drugs that were only modestly effective. Important clinical variables were selected, criteria for patient improvement determined, and an index was developed that distinguished treated patients from those getting placebo. This index (ACR 20/50/70) used in RA trials has led to approval of more than 20 drug therapies. Now that large-scale SLE clinical trial data exist, we propose to use the approach that was successful in RA. We will perform a post-hoc analysis of the raw data from the BLISS-52 and BLISS-76 trials investigating belimumab for SLE. The disease activity indices (SELENA SLEDAI and BILAG) will be deconstructed and individual clinical and laboratory parameters will be identified (for example, rash, complement). The variables that are present in the majority of patients, improve over time, and have face validity will be selected for this index. Both the physician global assessment and a patient-related measure of quality of life will be included. Study data will be split 50/50 into a training set and a validation set. Baseline values of variables will be compared with values at the end of the study to determine the degree of improvement or deterioration occurring in individual patients during the study. We will examine various threshold percent-improvement cutoff points across sets of variables, selecting those that produce the largest difference between placebo-treated and drug-treated patients while retaining an acceptably low proportion of improved placebo-treated patients. We will follow the methodology outlined by Harold Paulus in previous work for RA. The index will be tested by applying it to the remaining set of study subjects (validation set) used to derive the criterion. Performance measures will include discriminative ability, calibration and overall accuracy. This new composite index will be simple to use, based on real individual patient clinical trial data, and will include patient-reported outcome measures. The index should serve to prevent useful drugs from being discarded due to inadequate trial designs. Preliminary data will be presented.

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)0.323
metaresearch head score (Gemma)0.401
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesMetaresearch
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: none
GenreCandidate signal: Methods · Consensus signal: Methods
Teacher disagreement score0.323
Threshold uncertainty score0.835

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.3230.401
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0060.007
Bibliometrics0.0140.011
Science and technology studies0.0010.001
Scholarly communication0.0050.004
Open science0.0020.003
Research integrity0.0020.004
Insufficient payload (model declined to judge)0.0030.001

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 head0.329
GPT teacher head0.473
Teacher spread0.144 · 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.

Study designSimulation or modeling
Domainnot available
GenreMethods

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

Citations1
Published2014
Admission routes1
Has abstractyes

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