Publication:
Long-term Efficacy and Safety of Low-Dose and Dose-Escalating Interferon Alfa-2a Therapy in Refractory Behcet Uveitis

dc.contributor.authorAKMAN, MEHMET
dc.contributor.authorDİRESKENELİ, RAFİ HANER
dc.contributor.authorsOnal, Sumru; Kazokoglu, Haluk; Koc, Aylin; Akman, Mehmet; Bavbek, Tayfun; Direskeneli, Haner; Yavuz, Sule
dc.date.accessioned2022-03-14T09:16:18Z
dc.date.accessioned2026-01-11T19:01:16Z
dc.date.available2022-03-14T09:16:18Z
dc.date.issued2011-03-14
dc.description.abstractObjective: To investigate the long-term efficacy and safety of low-dose and dose-escalating therapy of interferon alfa-2a in the treatment of Behcet uveitis. Methods: This study included 37 patients with refractory Behcet panuveitis unresponsive to conventional immunosuppressive therapy. Induction interferon alfa-2a therapy was given as a daily dose of 3.0 million IU (MIU) subcutaneously for 14 days. Maintenance dose was achieved with 3.0 MIU 3 times per week given subcutaneously. The dosage was increased sequentially to 4.5, 6.0, and 9.0 MIU 3 times per week if uveitis relapses occurred. Total therapy duration was 24 months. Primary outcome measure was control of uveitis with quiescence during maintenance therapy. Ocular relapses per patient-year before and after initiation of interferon alfa-2a therapy and a corticosteroid-sparing effect were secondary outcomes. We also estimated the rate of remission after discontinuing interferon alfa-2a therapy. Results: During maintenance therapy, interferon alfa-2a controlled uveitis in 35 patients (95%). In 15 patients (41%), a maintenance dosage of 3.0 MIU 3 times per week controlled uveitis without any relapse. The rate of uveitis relapses decreased from 3.52 per patient-year before to 0.75 per patient-year after initiating interferon alfa-2a therapy. Seventeen patients were receiving systemic corticosteroids at the time of initiation of interferon therapy. During the maintenance stage, 9 patients were able to discontinue and 8 to taper systemic corticosteroid therapy. Survival analysis estimated that the rate of remission after discontinuation of interferon alfa-2a therapy was 76% by 3 months. The rate of remission remained stable thereafter. Conclusion: A treatment protocol using a low-dose and dose-escalating therapy with interferon alfa-2a was able to control and achieve remission of uveitis in most patients with refractory ocular Behcet disease.
dc.identifier.doi10.1001/archophthalmol.2011.3
dc.identifier.issn0003-9950
dc.identifier.pubmed21402983
dc.identifier.urihttps://hdl.handle.net/11424/242881
dc.identifier.wosWOS:000288326900006
dc.language.isoeng
dc.publisherAMER MEDICAL ASSOC
dc.relation.ispartofARCHIVES OF OPHTHALMOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDISEASE
dc.subjectPANUVEITIS
dc.subjectPOSTERIOR
dc.titleLong-term Efficacy and Safety of Low-Dose and Dose-Escalating Interferon Alfa-2a Therapy in Refractory Behcet Uveitis
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage294
oaire.citation.issue3
oaire.citation.startPage288
oaire.citation.titleARCHIVES OF OPHTHALMOLOGY
oaire.citation.volume129

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