Publication:
Certolizumab pegol in the treatment of Takayasu arteritis

dc.contributor.authorALİBAZ ÖNER, FATMA
dc.contributor.authorDİRESKENELİ, RAFİ HANER
dc.contributor.authorsNovikov, Pavel I.; Smitienko, Ilya O.; Sokolova, Maria V.; Alibaz-Oner, Fatma; Kaymaz-Tahra, Sema; Direskeneli, Haner; Moiseev, Sergey V.
dc.date.accessioned2022-03-14T08:41:31Z
dc.date.accessioned2026-01-11T13:14:28Z
dc.date.available2022-03-14T08:41:31Z
dc.date.issued2018-12-01
dc.description.abstractObjectives. Certolizumab pegol (CZP) is a PEGylated antigen-binding fragment-fragment of a humanized mAb neutralizing TNF. It lacks Fc-fragment and has a very low potential to cross the placenta. We aimed to report the efficacy and safety of CZP in a case series of patients with refractory Takayasu arteritis (TA). Methods. Ten females of reproductive age (18-35 years) with TA were treated with CZP (at a dose of 400 mg at weeks 0, 2 and 4 and at 200 mg every 2 weeks thereafter) for a median of 10 months (range 3-28). Prior to CZP administration all patients received glucocorticoids and +/- MTX, CYC, AZA, HCQ, LEF or MMF. Six patients were previously treated with other biological anti-cytokine drugs. The National Institutes of Health criteria and the Indian Takayasu Clinical Activity Score 2010 were used to define disease activity. Results. All patients rapidly responded to treatment with CZP and were able to taper prednisone and MTX doses. Treatment with CZP resulted in a significant decrease in median serum CRP levels and normalization of Indian Takayasu Clinical Activity Score 2010 score in 9 of 10 patients. Remission of systemic vasculitis was achieved in all patients. Seven patients maintained remission for at least 4 months, while one patient developed relapse after 2 years of CZP treatment. Side effects included mild infections (n = 5). Conclusion. Our case series suggests that CZP may be an effective and steroid-sparing treatment option in patients with active TA even if they did not previously respond to other TNF inhibitors or tocilizumab.
dc.identifier.doi10.1093/rheumatology/key197
dc.identifier.eissn1462-0332
dc.identifier.issn1462-0324
dc.identifier.pubmed30010945
dc.identifier.urihttps://hdl.handle.net/11424/242138
dc.identifier.wosWOS:000456557500009
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS
dc.relation.ispartofRHEUMATOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTNF inhibitors
dc.subjectcertolizumab pegol
dc.subjectTakayasu arteritis
dc.subjectANTIRHEUMATIC DRUGS
dc.subjectCASES SERIES
dc.subjectMULTICENTER
dc.subjectPREGNANCY
dc.subjectINHIBITORS
dc.subjectINFLIXIMAB
dc.subjectEFFICACY
dc.subjectCRITERIA
dc.subjectSTANDARD
dc.subjectALPHA
dc.titleCertolizumab pegol in the treatment of Takayasu arteritis
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage2105
oaire.citation.issue12
oaire.citation.startPage2101
oaire.citation.titleRHEUMATOLOGY
oaire.citation.volume57

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