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.author | Ekin, Ali | |
| dc.contributor.author | Mısırcı, Salim | |
| dc.contributor.author | Coşkun, Belkıs Nihan | |
| dc.contributor.author | Yağız, Burcu | |
| dc.contributor.author | Dalkiliç, Ediz | |
| dc.contributor.author | Pehlivan, Yavuz | |
| dc.contributor.buuauthor | EKİN, ALİ | |
| dc.contributor.buuauthor | MISIRCI, SALİM | |
| dc.contributor.buuauthor | COŞKUN, BELKIS NİHAN | |
| dc.contributor.buuauthor | YAĞIZ, BURCU | |
| dc.contributor.buuauthor | DALKILIÇ, HÜSEYİN EDİZ | |
| dc.contributor.buuauthor | PEHLİVAN, YAVUZ | |
| dc.contributor.department | Tıp Fakültesi | |
| dc.contributor.department | Romatoloji Bilim Dalı | |
| dc.contributor.orcid | 0000-0003-3692-1293 | |
| dc.contributor.scopusid | 57933090600 | |
| dc.contributor.scopusid | 57226710075 | |
| dc.contributor.scopusid | 55646165400 | |
| dc.contributor.scopusid | 13205593600 | |
| dc.contributor.scopusid | 6506739457 | |
| dc.contributor.scopusid | 57203458191 | |
| dc.date.accessioned | 2025-05-12T22:34:08Z | |
| dc.date.issued | 2024-01-01 | |
| dc.description.abstract | OBJECTIVE: 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.doi | 10.26355/eurrev_202405_36286 | |
| dc.identifier.endpage | 3522 | |
| dc.identifier.issn | 1128-3602 | |
| dc.identifier.issue | 10 | |
| dc.identifier.scopus | 2-s2.0-85195083597 | |
| dc.identifier.startpage | 3513 | |
| dc.identifier.uri | https://hdl.handle.net/11452/51369 | |
| dc.identifier.volume | 28 | |
| dc.indexed.scopus | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Verduci Editore s.r.l | |
| dc.relation.journal | European Review for Medical and Pharmacological Sciences | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Systemic lupus erythematosus | |
| dc.subject | Switching | |
| dc.subject | SLEDAI-2K | |
| dc.subject | Rituximab | |
| dc.subject | Biosimilar | |
| dc.subject.scopus | Innovative Therapies for Systemic Lupus Erythematosus | |
| dc.title | 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.type | Article | |
| dspace.entity.type | Publication | |
| local.contributor.department | Tıp Fakültesi/Romatoloji Bilim Dalı | |
| local.indexed.at | Scopus | |
| relation.isAuthorOfPublication | ee3ea25a-1fdc-4876-b08e-2b6a76d20984 | |
| relation.isAuthorOfPublication | 37ca4e99-defa-49d6-b361-86c008db6da1 | |
| relation.isAuthorOfPublication | faabfe30-a620-4cbe-8b6d-3db71b10ce0e | |
| relation.isAuthorOfPublication | 02b3cfbb-e8e7-4a95-b025-294888ae9a91 | |
| relation.isAuthorOfPublication | 1613225c-2f43-4052-9f82-210c854edcf4 | |
| relation.isAuthorOfPublication | 0075f2ae-ae8a-4690-bd46-128775e8efac | |
| relation.isAuthorOfPublication.latestForDiscovery | ee3ea25a-1fdc-4876-b08e-2b6a76d20984 |
