Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/11038
Title: Biosimilar filgrastim vs filgrastim: A multicenter nationwide observational bioequivalence study in patients with chemotherapy-induced neutropenia
Authors: Sevinç, A.
Özkan, M.
Özet, A.
Dane, F.
Öksüzoğlu, B.
Işikdoğan, A.
Özdemir, F.
Keywords: ANC recovery
Chemotherapy
Febrile neutropenia
Myelosuppressive
Neutrophil
Supportive care
biosimilar agent
biosimilar filgrastim
bleomycin
capecitabine
carboplatin
cisplatin
cyclophosphamide
cytarabine
dacarbazine
dexamethasone
docetaxel
doxorubicin
epirubicin
etoposide
filgrastim
fluorouracil
folinic acid
gemcitabine
ifosfamide
irinotecan
leucostim
methotrexate
oxaliplatin
paclitaxel
pemetrexed
tamoxifen
temozolomide
topotecan
trastuzumab
UFT
unclassified drug
unindexed drug
adult
aged
Article
bioequivalence
chemotherapy induced neutropenia
comparative effectiveness
drug efficacy
drug induced disease
hospital patient
human
major clinical study
multicenter study
neutropenia
neutrophil count
observational study
outpatient
Publisher: Dove Medical Press Ltd.
Abstract: Background: 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.
URI: https://hdl.handle.net/11499/11038
https://doi.org/10.2147/OTT.S106342
ISSN: 1178-6930
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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