Evidence map›Paper›PMID 40425263›Full record

ArticleLupus science & medicine2025

Long-term efficacy and safety of the Lupus-Cruces Nephritis protocol: a propensity score study of the Lupus-Cruces and Lupus-Bordeaux cohorts.

Guillermo Ruiz-Irastorza, Beatriz Marín-García, Luis Dueña-Bartolomé, Diana Paredes Ruiz, Amaia Osorio, Estibaliz Lazaro

Abstract read
In one paragraph

Article in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  4. Observational
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4 · The record

Corrections and comments

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

6 authors.

Guillermo Ruiz-IrastorzaAutoimmune Diseases, Instituto de Investigación Sanitaria Biobizkaia, Barakaldo, Spain guillermo.ruiz@ehu.eus.ORCID 0000-0001-7788-1043
Beatriz Marín-GarcíaAutoimmune Diseases, Instituto de Investigación Sanitaria Biobizkaia, Barakaldo, Spain.ORCID 0009-0001-1007-5378
Luis Dueña-BartoloméAutoimmune Diseases, Instituto de Investigación Sanitaria Biobizkaia, Barakaldo, Spain.ORCID 0000-0001-8256-9353
Diana Paredes RuizAutoimmune Diseases, Instituto de Investigación Sanitaria Biobizkaia, Barakaldo, Spain.ORCID 0000-0001-8378-8638
Amaia OsorioDepartment of Nephrology, Cruces University Hospital, Barakaldo, Spain.ORCID 0000-0002-9842-1553
Estibaliz LazaroDepartment of Internal Medicine and Infectious Diseases, Bordeaux University Hospital, Pessac, France.ORCID 0000-0002-4206-7399

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the efficacy and toxicity of the Lupus-Cruces Nephritis (LCN) protocol compared with standard of care (SOC) with cyclophosphamide (CYC) or mycophenolate in patients with lupus nephritis (LN) during an extended follow-up time up to 10 years.

methodsPatients with biopsy-proven class III, IV or V LN treated with LCN were compared with SOC. Patients in the LCN were treated with a CYC plus repeated methylprednisolone pulse-based regimen. The achievement of complete renal response (CRR) and the progression to chronic kidney disease (CKD) were the two main outcomes. Glucocorticoid (GC)-related toxicity, major infections and damage accrual were also analysed. A propensity score (PS)-adjusted multivariate analysis was used to overcome the confounding-by-indication bias.

results147 patients were included in this study (47 LCN and 100 SOC). CRR at 12 months was 85% vs 44%, respectively (p<0.001). Eventually, 96% patients in the LCN group achieved CRR vs 74% patients in the SOC (p=0.002). In the multivariate PS-adjusted Cox model, LCN patients were more likely to eventually achieve CRR (PS-adjusted HR 3.5, 95% CI 2.2 to 5.5, p<0.001). The risk of progression to CKD was lower in LCN patients (PS-adjusted HR 0.3, 95% CI 0.11 to 0.82, p=0.019). The risks of GC-induced toxicity, renal or GC-related damage accrual and major infections were also lower in the LCN group: adjusted HR 0.09, 95% CI 0.02 to 0.39; PS-adjusted HR 0.14, 95% CI 0.04 to 0.4; PS-adjusted HR 0.2, 95% CI 0.046 to 0.95; respectively.

conclusionsThis study confirms the LCN protocol as an effective and safe, in addition to widely available and affordable, regimen for the induction therapy of LN.

Indexed as

CyclophosphamideImmunosuppressive AgentsLupus NephritisMycophenolic AcidAdultDisease ProgressionDrug Therapy, CombinationFemaleFollow-Up StudiesGlucocorticoidsHumansMaleMethylprednisoloneMiddle AgedPropensity ScoreRenal Insufficiency, ChronicCyclophosphamideGlucocorticoidsImmunosuppressive AgentsMethylprednisoloneMycophenolic AcidCyclophosphamideGlucocorticoidsLupus NephritisSystemic Lupus Erythematosus

Identifiers

PMID40425263
PMCPMC12107586

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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.