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Title:Current treatment in macrophage activation syndrome worldwide : a systematic literature review to inform the METAPHOR project
Authors:ID Baldo, Francesco (Author)
ID Erkens, Remco G. A. (Author)
ID Mizuta, Mao (Author)
ID Rogani, Greta (Author)
ID Lucioni, Federica (Author)
ID Bracaglia, Claudia (Author)
ID Foell, Dirk (Author)
ID Gattorno, Marco (Author)
ID Jelusic, Marija (Author)
ID Toplak, Nataša (Research coworker), et al.
Files:.pdf PDF - Presentation file, download (1,08 MB)
MD5: FE53AFC8FC2626DE1E2790AFFBDA5D50
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Objective: To assess current treatment in macrophage activation syndrome (MAS) worldwide and to highlight any areas of major heterogeneity of practice. Methods: A systematic literature search was performed in both EMBASE and PubMed databases. Paper screening was done by two independent teams based on agreed criteria. Data extraction was standardized following the PICO framework. A panel of experts assessed paper validity, using the Joanna Briggs Institute appraisal tools and category of evidence (CoE) according to EULAR procedure. Results: Fifty-seven papers were finally included (80% retrospective case-series), describing 1148 patients with MAS: 889 systemic juvenile idiopathic arthritis (sJIA), 137 systemic lupus erythematosus (SLE), 69 Kawasaki disease (KD) and 53 other rheumatological conditions. Fourteen and 11 studies specified data on MAS associated to SLE and KD, respectively. All papers mentioned glucocorticoids (GCs), mostly methylprednisolone and prednisolone (90%); dexamethasone was used in 7% of patients. Ciclosporin was reported in a wide range of patients according to different cohorts. Anakinra was used in 179 MAS patients, with a favourable outcome in 83% of sJIA-MAS. Etoposide was described by 11 studies, mainly as part of HLH-94/04 protocol. Emapalumab was the only medication tested in a clinical trial in 14 sJIA-MAS, with 93% of MAS remission. Ruxolitinib was the most reported Janus kinase inhibitor in MAS. Conclusion: High-dose GCs together with IL-1 and IFNγ inhibitors have shown efficacy in MAS, especially in sJIA-associated MAS. However, the global level of evidence on MAS treatment, especially in other conditions, is still poor and requires standardized studies to be confirmed.
Keywords:macrophage activation syndrome, haemophagocytic syndromes, haemophagocytic lymphohistiocytosis, treatment
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:str. 32–44
Numbering:Vol. 64, iss. 1
PID:20.500.12556/DiRROS-29060 New window
UDC:616-002
ISSN on article:1462-0332
DOI:10.1093/rheumatology/keae391 New window
COBISS.SI-ID:244719619 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 4. 8. 2025;
Publication date in DiRROS:20.04.2026
Views:111
Downloads:52
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Record is a part of a journal

Title:Rheumatology
Shortened title:Rheumatol.
Publisher:Oxford University Press
ISSN:1462-0332
COBISS.SI-ID:515393817 New window

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License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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