Mycophenolate mofetil for methotrexate-resistant juvenile localized scleroderma.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
02 03 2021
Historique:
received: 30 03 2020
revised: 08 06 2020
pubmed: 27 9 2020
medline: 30 6 2021
entrez: 26 9 2020
Statut: ppublish

Résumé

To investigate safety and efficacy of MMF in patients with severe or MTX-refractory juvenile localized scleroderma. Consecutive juvenile localized scleroderma patients undergoing systemic treatment were included in a retrospective longitudinal study. Patients treated with MMF because they were refractory or intolerant to MTX (MMF-group) were compared with responders to MTX (MTX-group). Disease activity was assessed by Localized Scleroderma Cutaneous Assessment Tool and thermography. Disease course was established on the number of relapses and treatment changes. Relapse-free survival was examined by Kaplan-Meier analysis. MMF and MTX groups included 22 and 47 patients, respectively. No significant difference in demographics, follow-up duration and treatment before diagnosis was observed between groups. The most represented clinical subtypes in the MMF-group were pansclerotic morphea and mixed subtype (P = 0.008 and P = 0.029, respectively), and linear scleroderma of the face in the MTX-group (P = 0.048). MMF was started because of MTX resistance (18 patients), relapse during MTX tapering/withdrawal (3 patients) and anaphylaxis to MTX (1 patient). After mean 9.4 years of follow-up, 90.9% of patients on MMF and 100% of those on MTX had inactive disease. No significant difference in relapse-free survival between the groups was found (P = 0.066, log-rank test), although MMF likely induced more persistent remission. MMF was well tolerated and combination of MMF and MTX did not increase its efficacy. The present study adds strong evidence on the efficacy and tolerance of MMF in severe and/or MTX-refractory juvenile localized scleroderma. Further controlled studies are needed to prove its efficacy as first line treatment.

Identifiants

pubmed: 32978631
pii: 5911878
doi: 10.1093/rheumatology/keaa392
pmc: PMC7937018
doi:

Substances chimiques

Antirheumatic Agents 0
Mycophenolic Acid HU9DX48N0T
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1387-1391

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Giorgia Martini (G)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

Laura Saggioro (L)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

Roberta Culpo (R)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

Fabio Vittadello (F)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

Alessandra Meneghel (A)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

Francesco Zulian (F)

Paediatric Rheumatology Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

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Classifications MeSH