Biosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropenia

dc.contributor.authorSevinç, Alper
dc.contributor.authorÖzkan, Metin
dc.contributor.authorÖzet, Ahmet
dc.contributor.authorDane, Faysal
dc.contributor.authorÖksüzoğlu, Berna
dc.contributor.authorIşıkdoğan, Abdurrahman
dc.contributor.authorÖzdemir, Feyyaz
dc.contributor.authorUncu, Doğan
dc.contributor.authorGümüş, Mahmut
dc.contributor.authorYaren, Arzu
dc.contributor.authorKara, Oğuz
dc.contributor.authorTekin, Salim Başol
dc.contributor.buuauthorEvrensel, Türkkan
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Onkoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-9732-5340tr_TR
dc.contributor.researcheridAAJ-1027-2021tr_TR
dc.contributor.scopusid6603942124tr_TR
dc.date.accessioned2023-10-20T05:57:23Z
dc.date.available2023-10-20T05:57:23Z
dc.date.issued2018
dc.description.abstractBackground: We studied the comparative effectiveness of biosimilar filgrastim vs original filgrastim in patients with chemotherapy-induced neutropenia. Patients and methods: This multicenter, observational study was conducted at 14 centers. The study included 337 patients experiencing neutropenia under chemotherapy. Patients were given either filgrastim 30 MIU or 48 MIU (Neupogen (R)) or biosimilar filgrastim 30 MIU (Leucostim (R)). Data regarding age, chemotherapeutic agents used, number of chemotherapy courses, previous diagnosis of neutropenia, neutrophil count of patients after treatment, medications used for the treatment of neutropenia, and duration of neutropenia were collected. Time to absolute neutrophil count (ANC) recovery was the primary efficacy measure. Results: Ambulatory and hospitalized patients comprised 11.3% and 45.1% of the enrolled patients, respectively, and a previous diagnosis of neutropenia was reported in 49.3% of the patients, as well. Neutropenia occurred in 13.7% (n=41), 45.5% (n=136), 27.4% (n=82), 11.4% (n=34), and 2.0% (n=6) of the patients during the first, second, third, fourth, and fifth cycles of chemotherapy, respectively. While the mean neutrophil count was 0.53 +/- 0.48 before treatment, a significant increase to 2.44 +/- 0.66 was observed after treatment (p=0.0001). While 90.3% of patients had a neutrophil count,1.49 before treatment, all patients had a neutrophil count >= 1.50 after treatment. Neutropenia resolved within <= 4 days of filgrastim therapy in 60.1%, 56.7%, and 52.6% of the patients receiving biosimilar filgrastim 30 MIU, original filgrastim 30 MIU, and original filgrastim 48 MIU, respectively. However, there was no significant difference between the three arms (p=0.468). Similarly, time to ANC recovery was comparable between the treatment arms (p=0.332). Conclusion: The results indicate that original filgrastim and biosimilar filgrastim have comparable efficacy in treating neutropenia. Biosimilar filgrastim provides a valuable alternative; however, there is need for further studies comparing the two products in different patient subpopulations.en_US
dc.identifier.citationSevinç, A. vd. (2018). ''Biosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropenia''. OncoTargets and Therapy, 11, 419-426.en_US
dc.identifier.endpage426tr_TR
dc.identifier.issn1178-6930
dc.identifier.pubmed29403286tr_TR
dc.identifier.scopus2-s2.0-85040948324tr_TR
dc.identifier.startpage419tr_TR
dc.identifier.urihttps://doi.org/10.2147/OTT.S106342
dc.identifier.urihttps://www.dovepress.com/biosimilar-filgrastim-vs-filgrastim-a-multicenter-nationwide-observati-peer-reviewed-fulltext-article-OTT
dc.identifier.urihttp://hdl.handle.net/11452/34472
dc.identifier.volume11tr_TR
dc.identifier.wos000422656100001
dc.indexed.pubmedPubMeden_US
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherDove Medical Pressen_US
dc.relation.collaborationYurt içitr_TR
dc.relation.journalOncoTargets and Therapyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBiotechnology & applied microbiologyen_US
dc.subjectOncologyen_US
dc.subjectChemotherapyen_US
dc.subjectFebrile neutropeniaen_US
dc.subjectNeutrophilen_US
dc.subjectANC recoveryen_US
dc.subjectSupportive careen_US
dc.subjectMyelosuppressiveen_US
dc.subjectColony-stimulating factoren_US
dc.subjectNon-hodgkins-lymphomaen_US
dc.subjectFebrile neutropeniaen_US
dc.subjectG-csfen_US
dc.subjectReceiving chemotherapyen_US
dc.subjectCancer-chemotherapyen_US
dc.subjectBreast-canceren_US
dc.subjectLung-cancerrisken_US
dc.subjectChopen_US
dc.subject.emtreeBiosimilar agenten_US
dc.subject.emtreeBiosimilar filgrastimen_US
dc.subject.emtreeBleomycinen_US
dc.subject.emtreeCapecitabineen_US
dc.subject.emtreeCarboplatinen_US
dc.subject.emtreeCisplatinen_US
dc.subject.emtreeCyclophosphamideen_US
dc.subject.emtreeCytarabineen_US
dc.subject.emtreeDacarbazineen_US
dc.subject.emtreeDexamethasoneen_US
dc.subject.emtreeDocetaxelen_US
dc.subject.emtreeDoxorubicinen_US
dc.subject.emtreeEpirubicinen_US
dc.subject.emtreeEtoposideen_US
dc.subject.emtreeFilgrastimen_US
dc.subject.emtreeFluorouracilen_US
dc.subject.emtreeFolinic aciden_US
dc.subject.emtreeGemcitabineen_US
dc.subject.emtreeIosfamideen_US
dc.subject.emtreeIrinotecanen_US
dc.subject.emtreeLeucostimen_US
dc.subject.emtreeMethotrexateen_US
dc.subject.emtreeOxaliplatinen_US
dc.subject.emtreePaclitaxelen_US
dc.subject.emtreePemetrexeden_US
dc.subject.emtreeTamoxifenen_US
dc.subject.emtreeTemozolomideen_US
dc.subject.emtreeTopotecanen_US
dc.subject.emtreeTrastuzumaben_US
dc.subject.emtreeUFTen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeUnindexed drugen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBioequivalenceen_US
dc.subject.emtreeChemotherapy induced neutropeniaen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeComparative effectivenessen_US
dc.subject.emtreeDrug induced diseaseen_US
dc.subject.emtreeHospital patienten_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMulticenter studyen_US
dc.subject.emtreeNeutropeniaen_US
dc.subject.emtreeNeutrophil counten_US
dc.subject.emtreeObservational studyen_US
dc.subject.emtreeOutpatienten_US
dc.subject.scopusPegfilgrastim; Febrile Neutropenia; Chemotherapyen_US
dc.subject.wosBiotechnology & applied microbiologyen_US
dc.subject.wosOncologyen_US
dc.titleBiosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropeniaen_US
dc.typeArticle
dc.wos.quartileQ2en_US

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