Publication:
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.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Onkoloji Ana Bilim Dalı
dc.contributor.orcid0000-0002-9732-5340
dc.contributor.researcheridAAJ-1027-2021
dc.contributor.scopusid6603942124
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.
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.
dc.identifier.endpage426
dc.identifier.issn1178-6930
dc.identifier.pubmed29403286
dc.identifier.scopus2-s2.0-85040948324
dc.identifier.startpage419
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.volume11
dc.identifier.wos000422656100001
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherDove Medical Press
dc.relation.collaborationYurt içi
dc.relation.journalOncoTargets and Therapy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBiotechnology & applied microbiology
dc.subjectOncology
dc.subjectChemotherapy
dc.subjectFebrile neutropenia
dc.subjectNeutrophil
dc.subjectANC recovery
dc.subjectSupportive care
dc.subjectMyelosuppressive
dc.subjectColony-stimulating factor
dc.subjectNon-hodgkins-lymphoma
dc.subjectFebrile neutropenia
dc.subjectG-csf
dc.subjectReceiving chemotherapy
dc.subjectCancer-chemotherapy
dc.subjectBreast-cancer
dc.subjectLung-cancerrisk
dc.subjectChop
dc.subject.emtreeBiosimilar agent
dc.subject.emtreeBiosimilar filgrastim
dc.subject.emtreeBleomycin
dc.subject.emtreeCapecitabine
dc.subject.emtreeCarboplatin
dc.subject.emtreeCisplatin
dc.subject.emtreeCyclophosphamide
dc.subject.emtreeCytarabine
dc.subject.emtreeDacarbazine
dc.subject.emtreeDexamethasone
dc.subject.emtreeDocetaxel
dc.subject.emtreeDoxorubicin
dc.subject.emtreeEpirubicin
dc.subject.emtreeEtoposide
dc.subject.emtreeFilgrastim
dc.subject.emtreeFluorouracil
dc.subject.emtreeFolinic acid
dc.subject.emtreeGemcitabine
dc.subject.emtreeIosfamide
dc.subject.emtreeIrinotecan
dc.subject.emtreeLeucostim
dc.subject.emtreeMethotrexate
dc.subject.emtreeOxaliplatin
dc.subject.emtreePaclitaxel
dc.subject.emtreePemetrexed
dc.subject.emtreeTamoxifen
dc.subject.emtreeTemozolomide
dc.subject.emtreeTopotecan
dc.subject.emtreeTrastuzumab
dc.subject.emtreeUFT
dc.subject.emtreeUnclassified drug
dc.subject.emtreeUnindexed drug
dc.subject.emtreeAdult
dc.subject.emtreeAged
dc.subject.emtreeArticle
dc.subject.emtreeBioequivalence
dc.subject.emtreeChemotherapy induced neutropenia
dc.subject.emtreeDrug efficacy
dc.subject.emtreeComparative effectiveness
dc.subject.emtreeDrug induced disease
dc.subject.emtreeHospital patient
dc.subject.emtreeHuman
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMulticenter study
dc.subject.emtreeNeutropenia
dc.subject.emtreeNeutrophil count
dc.subject.emtreeObservational study
dc.subject.emtreeOutpatient
dc.subject.scopusPegfilgrastim; Febrile Neutropenia; Chemotherapy
dc.subject.wosBiotechnology & applied microbiology
dc.subject.wosOncology
dc.titleBiosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropenia
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Onkoloji Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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