Management of lupus nephritis: a systematic literature review informing the 2019 update of the joint EULAR and European Renal Association-European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations.
Biomarkers
Biopsy
Calcineurin
/ administration & dosage
Clinical Decision-Making
Disease Management
Disease Susceptibility
Drug Resistance
Humans
Immunosuppressive Agents
/ administration & dosage
Kidney
/ immunology
Kidney Failure, Chronic
/ diagnosis
Lupus Nephritis
/ complications
Molecular Targeted Therapy
Practice Guidelines as Topic
Severity of Illness Index
Treatment Outcome
Lupus Erythematosus
Lupus Nephritis
Systemic
Therapeutics
Journal
RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
07
04
2020
revised:
08
05
2020
accepted:
22
05
2020
entrez:
24
7
2020
pubmed:
24
7
2020
medline:
11
6
2021
Statut:
ppublish
Résumé
To analyse the current evidence for the management of lupus nephritis (LN) informing the 2019 update of the EULAR/European Renal Association-European Dialysis and Transplant Association recommendations. According to the EULAR standardised operating procedures, a PubMed systematic literature review was performed, from January 1, 2012 to December 31, 2018. Since this was an update of the 2012 recommendations, the final level of evidence (LoE) and grading of recommendations considered the total body of evidence, including literature prior to 2012. We identified 387 relevant articles. High-quality randomised evidence supports the use of immunosuppressive treatment for class III and class IV LN (LoE 1a), and moderate-level evidence supports the use of immunosuppressive treatment for pure class V LN with nephrotic-range proteinuria (LoE 2b). Treatment should aim for at least 25% reduction in proteinuria at 3 months, 50% at 6 months and complete renal response (<500-700 mg/day) at 12 months (LoE 2a-2b). High-quality evidence supports the use of mycophenolate mofetil/mycophenolic acid (MMF/MPA) or low-dose intravenous cyclophosphamide (CY) as initial treatment of active class III/IV LN (LoE 1a). Combination of tacrolimus with MMF/MPA and high-dose CY are alternatives in specific circumstances (LoE 1a). There is low-quality level evidence to guide optimal duration of immunosuppression in LN (LoE 3). In end-stage kidney disease, all methods of kidney replacement treatment can be used, with transplantation having the most favourable outcomes (LoE 2b). There is high-quality evidence to guide the initial and subsequent phases of class III/IV LN treatment, but low-to-moderate quality evidence to guide treatment of class V LN, monitoring and optimal duration of immunosuppression.
Identifiants
pubmed: 32699043
pii: rmdopen-2020-001263
doi: 10.1136/rmdopen-2020-001263
pmc: PMC7425195
pii:
doi:
Substances chimiques
Biomarkers
0
Immunosuppressive Agents
0
Calcineurin
EC 3.1.3.16
Types de publication
Journal Article
Meta-Analysis
Research Support, Non-U.S. Gov't
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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