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Record W4297294679 · doi:10.1136/lupus-2022-elm2022.14

S06.2 Long-term efficacy and safety of voclosporin with mmf and low-dose steroids: data from the aurora 2 continuation study

2022· article· en· W4297294679 on OpenAlexaff
Keisha L. Gibson, Y Teng, L Hodge, C Collins

Bibliographic record

Venuenot available
Typearticle
Languageen
FieldMedicine
TopicSystemic Lupus Erythematosus Research
Canadian institutionsAurinia (Canada)
Fundersnot available
KeywordsMedicineLupus nephritisUrologyRenal functionProteinuriaAdverse effectPlaceboCalcineurinInternal medicineGastroenterologyPharmacologyKidneyTransplantationPathologyDisease

Abstract

fetched live from OpenAlex

Purpose Voclosporin is a novel calcineurin inhibitor approved in the United States in January 2021 for the treatment of adult patients with active lupus nephritis in combination with background immunosuppressive therapy. The Phase 3 AURORA 1 study showed that adding voclosporin to mycophenolate mofetil (MMF) and low-dose steroids led to significantly greater reductions in proteinuria at 52 weeks. Given the potentially serious safety concerns associated with the long-term use of oral steroids, we evaluated the safety and efficacy of treatment with voclosporin in patients maintained on low-dose steroids for an additional 24 months in the AURORA 2 continuation study. Methods Key inclusion criteria for the parent AURORA 1 study included biopsy-proven active lupus nephritis (Class III, IV, or V ± III/IV), proteinuria ≥1.5 mg/mg (≥2 mg/mg for Class V) and estimated glomerular filtration rate (eGFR) >45 mL/min/1.73 m2. Patients who completed AURORA 1 were eligible to enroll in AURORA 2 on the same blinded treatment of voclosporin or placebo in combination with MMF (target dose 2 g/day) and low-dose oral steroids. Per-protocol steroid use in AURORA 1 required a rapid taper from a starting dose of 20–25 mg/day to a target of ≤2.5 mg/day by Week 16. The final dose of steroids in AURORA 1 was the initial starting dose in AURORA 2; the dose could then be adjusted further at the discretion of the study investigator. AURORA 2 was not designed nor powered to address the impact of voclosporin on oral steroid dose. Results In total, 116 patients in the voclosporin arm and 100 patients in the control arm enrolled in AURORA 2. The efficacy observed in patients treated with voclosporin in AURORA 1 was maintained throughout AURORA 2 as indicated by the greater Least Square (LS) mean reductions in UPCR from baseline in the voclosporin arm vs. control arm at all time points (Figure 1A). The overall exposure to oral steroids during the study was similar for both treatment arms; over three years of treatment, the majority of patients were on steroid doses ≤2.5 mg/day (Table 1). There were no new or unexpected safety signals detected in patients who continued on voclosporin treatment compared to control-treated patients with similar rates of serious adverse events in the voclosporin (18.1%) and control arms (23.0%). There were no deaths in the voclosporin arm during AURORA 2; four deaths were reported in the control arm (pulmonary embolism [n=1], coronavirus infection [n=3]). Mean eGFR remained stable throughout the study (Figure 1B). Conclusions Voclosporin was safe and well-tolerated over three years of treatment with a similar safety profile to control and no unexpected safety signals detected. Further, the significant reductions in proteinuria initially achieved in AURORA 1 were maintained in AURORA 2 even in the absence of traditional high-dose steroids. These data provide evidence of a long-term treatment benefit of voclosporin in patients with lupus nephritis and also support the use of lower doses of steroids in the treatment of this disease.

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 score0.013
Threshold uncertainty score0.042

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0040.003
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.003
Bibliometrics0.0000.001
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0020.003
Insufficient payload (model declined to judge)0.0130.003

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 head0.049
GPT teacher head0.327
Teacher spread0.279 · 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".

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Citations0
Published2022
Admission routes1
Has abstractyes

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