New potential weapons for refractory scleritis in the era of targeted therapy

dc.contributor.authorFabiani, Claudia
dc.contributor.authorSota, Jurgen
dc.contributor.authorSainz de la Maza Serra, María Teresa
dc.contributor.authorPelegrin, Laura
dc.contributor.authorEmmi, Giacomo
dc.contributor.authorLopalco, Giuseppe
dc.contributor.authorIannone, Florenzo
dc.contributor.authorVannozzi, Lorenzo
dc.contributor.authorGuerriero, Silvana
dc.contributor.authorGelmi, Maria Chiara
dc.contributor.authorRigante, Donato
dc.contributor.authorTosi, Gian Marco
dc.contributor.authorHernández Rodríguez, José
dc.contributor.authorCantarini, Luca
dc.date.accessioned2021-04-22T18:49:39Z
dc.date.available2021-04-22T18:49:39Z
dc.date.issued2020-01-17
dc.date.updated2021-04-22T18:49:39Z
dc.description.abstractObjective. To assess the efficacy of biologic drugs, beyond tumor necrosis factor- (TNF-) α inhibitors, in the management of noninfectious refractory scleritis, either idiopathic or associated with systemic immune-mediated disorders. Patients and Methods. This is a retrospective study assessing the efficacy of several biologic agents (rituximab, anakinra, tocilizumab, and abatacept) and the small molecule tofacitinib in the treatment of scleritis through assessment of scleral inflammation and relapses, as well as treatment impact on best-corrected visual acuity (BCVA) and safety profile. Results. Fourteen patients (19 eyes) were enrolled in the study. Scleritis inflammatory grading significantly improved from baseline to 3 months (p=0.002) and from baseline to the last follow-up visit (p=0.002). Scleritis relapses significantly decreased between the 12 months preceding and following biologic therapy (p=0.007). No differences regarding BCVA were observed (p=0.67). Regarding adverse events, only one patient developed pneumonia and septic shock under rituximab treatment. Conclusions. Our results, though limited to a low number of patients, highlight the effectiveness of different biologic therapies in the treatment of noninfectious refractory scleritis, showing to control scleral inflammation and allowing a significant reduction in the number of relapses.
dc.format.extent7 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec703626
dc.identifier.issn0962-9351
dc.identifier.pmid32410867
dc.identifier.urihttps://hdl.handle.net/2445/176669
dc.language.isoeng
dc.publisherHindawi
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1155/2020/8294560
dc.relation.ispartofMediators of Inflammation, 2020, vol. 2020, p. 8294560
dc.relation.urihttps://doi.org/10.1155/2020/8294560
dc.rightscc-by (c) Fabiani, Claudia et al., 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationAssaigs clínics de medicaments
dc.subject.classificationInflamació
dc.subject.classificationDianes farmacològiques
dc.subject.otherDrug testing
dc.subject.otherInflammation
dc.subject.otherDrug targeting
dc.titleNew potential weapons for refractory scleritis in the era of targeted therapy
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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