Yayın:
The retrospective evaluation of efficacy and safety data after switching from originator rituximab to biosimilar rituximab (CT-P10) in patients diagnosed with systemic lupus erythematosus: A single-center experience

dc.contributor.authorEkin, Ali
dc.contributor.authorMısırcı, Salim
dc.contributor.authorCoşkun, Belkıs Nihan
dc.contributor.authorYağız, Burcu
dc.contributor.authorDalkiliç, Ediz
dc.contributor.authorPehlivan, Yavuz
dc.contributor.buuauthorEKİN, ALİ
dc.contributor.buuauthorMISIRCI, SALİM
dc.contributor.buuauthorCOŞKUN, BELKIS NİHAN
dc.contributor.buuauthorYAĞIZ, BURCU
dc.contributor.buuauthorDALKILIÇ, HÜSEYİN EDİZ
dc.contributor.buuauthorPEHLİVAN, YAVUZ
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentRomatoloji Bilim Dalı
dc.contributor.orcid0000-0003-3692-1293
dc.contributor.scopusid57933090600
dc.contributor.scopusid57226710075
dc.contributor.scopusid55646165400
dc.contributor.scopusid13205593600
dc.contributor.scopusid6506739457
dc.contributor.scopusid57203458191
dc.date.accessioned2025-05-12T22:34:08Z
dc.date.issued2024-01-01
dc.description.abstractOBJECTIVE: In our study, we analyzed the efficacy and safety data of patients with systemic lupus erythematosus (SLE) after switching to biosimilar rituximab (RTX). PATIENTS AND METHODS: Twenty-two patients who switched to RTX were included in the study. Efficacy data were analyzed using the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score, and safety data were analyzed using the frequency of side effects. RESULTS: The mean treatment duration of originator RTX was 35.6 ± 23.0 months, and the median treatment duration of biosimilar RTX was 17 months. The SLEDAI-2K score, approximately three months after the first dose of biosimilar RTX, was significantly lower (p = 0.027). A statistically significant difference was found between the SLEDAI-2K score assessed at the follow-up visit three months after the last dose of originator RTX and the SLEDAI-2K score obtained approximately three months after the first dose of biosimilar RTX (p = 0.011) and the calculated median SLEDAI-2K score was significantly lower than the SLEDAI-2K score assessed after administration of originator RTX. The side effect frequency that developed during the treatment of originator RTX was 15.3 per 100 patient-years. The most common side effect was infection, which was 15.3 per 100 patient-years. The most frequent infection was urinary tract infection. The side effect frequency during treatment of biosimilar RTX was 39 per 100 patient-years, and the most frequent infection was pneumonia. CONCLUSIONS: In our study, SLEDAI-2K scores demonstrated that no efficacy loss was experienced after switching to CT-P10 molecule, which is a biosimilar RTX. It was observed that switching to biosimilar RTX did not decrease treatment efficacy in the patient group diagnosed with SLE and biosimilar RTX was found to be safe.
dc.identifier.doi10.26355/eurrev_202405_36286
dc.identifier.endpage3522
dc.identifier.issn1128-3602
dc.identifier.issue10
dc.identifier.scopus2-s2.0-85195083597
dc.identifier.startpage3513
dc.identifier.urihttps://hdl.handle.net/11452/51369
dc.identifier.volume28
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherVerduci Editore s.r.l
dc.relation.journalEuropean Review for Medical and Pharmacological Sciences
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSystemic lupus erythematosus
dc.subjectSwitching
dc.subjectSLEDAI-2K
dc.subjectRituximab
dc.subjectBiosimilar
dc.subject.scopusInnovative Therapies for Systemic Lupus Erythematosus
dc.titleThe retrospective evaluation of efficacy and safety data after switching from originator rituximab to biosimilar rituximab (CT-P10) in patients diagnosed with systemic lupus erythematosus: A single-center experience
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Romatoloji Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublicationee3ea25a-1fdc-4876-b08e-2b6a76d20984
relation.isAuthorOfPublication37ca4e99-defa-49d6-b361-86c008db6da1
relation.isAuthorOfPublicationfaabfe30-a620-4cbe-8b6d-3db71b10ce0e
relation.isAuthorOfPublication02b3cfbb-e8e7-4a95-b025-294888ae9a91
relation.isAuthorOfPublication1613225c-2f43-4052-9f82-210c854edcf4
relation.isAuthorOfPublication0075f2ae-ae8a-4690-bd46-128775e8efac
relation.isAuthorOfPublication.latestForDiscoveryee3ea25a-1fdc-4876-b08e-2b6a76d20984

Dosyalar