Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/11038
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dc.contributor.authorSevinç, A.-
dc.contributor.authorÖzkan, M.-
dc.contributor.authorÖzet, A.-
dc.contributor.authorDane, F.-
dc.contributor.authorÖksüzoğlu, B.-
dc.contributor.authorIşikdoğan, A.-
dc.contributor.authorÖzdemir, F.-
dc.date.accessioned2019-08-16T13:34:39Z
dc.date.available2019-08-16T13:34:39Z
dc.date.issued2018-
dc.identifier.issn1178-6930-
dc.identifier.urihttps://hdl.handle.net/11499/11038-
dc.identifier.urihttps://doi.org/10.2147/OTT.S106342-
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®) or biosimilar filgrastim 30 MIU (Leucostim®). 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. © 2018 Sevinç et al.en_US
dc.language.isoenen_US
dc.publisherDove Medical Press Ltd.en_US
dc.relation.ispartofOncoTargets and Therapyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectANC recoveryen_US
dc.subjectChemotherapyen_US
dc.subjectFebrile neutropeniaen_US
dc.subjectMyelosuppressiveen_US
dc.subjectNeutrophilen_US
dc.subjectSupportive careen_US
dc.subjectbiosimilar agenten_US
dc.subjectbiosimilar filgrastimen_US
dc.subjectbleomycinen_US
dc.subjectcapecitabineen_US
dc.subjectcarboplatinen_US
dc.subjectcisplatinen_US
dc.subjectcyclophosphamideen_US
dc.subjectcytarabineen_US
dc.subjectdacarbazineen_US
dc.subjectdexamethasoneen_US
dc.subjectdocetaxelen_US
dc.subjectdoxorubicinen_US
dc.subjectepirubicinen_US
dc.subjectetoposideen_US
dc.subjectfilgrastimen_US
dc.subjectfluorouracilen_US
dc.subjectfolinic aciden_US
dc.subjectgemcitabineen_US
dc.subjectifosfamideen_US
dc.subjectirinotecanen_US
dc.subjectleucostimen_US
dc.subjectmethotrexateen_US
dc.subjectoxaliplatinen_US
dc.subjectpaclitaxelen_US
dc.subjectpemetrexeden_US
dc.subjecttamoxifenen_US
dc.subjecttemozolomideen_US
dc.subjecttopotecanen_US
dc.subjecttrastuzumaben_US
dc.subjectUFTen_US
dc.subjectunclassified drugen_US
dc.subjectunindexed drugen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectArticleen_US
dc.subjectbioequivalenceen_US
dc.subjectchemotherapy induced neutropeniaen_US
dc.subjectcomparative effectivenessen_US
dc.subjectdrug efficacyen_US
dc.subjectdrug induced diseaseen_US
dc.subjecthospital patienten_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmulticenter studyen_US
dc.subjectneutropeniaen_US
dc.subjectneutrophil counten_US
dc.subjectobservational studyen_US
dc.subjectoutpatienten_US
dc.titleBiosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropeniaen_US
dc.typeArticleen_US
dc.identifier.volume11en_US
dc.identifier.startpage419
dc.identifier.startpage419en_US
dc.identifier.endpage426en_US
dc.identifier.doi10.2147/OTT.S106342-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid29403286en_US
dc.identifier.scopus2-s2.0-85040948324en_US
dc.identifier.wosWOS:000422656100001en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
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Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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