» Articles » PMID: 26858523

Lipegfilgrastim in the Management of Chemotherapy-induced Neutropenia of Cancer Patients

Overview
Journal Biologics
Date 2016 Feb 10
PMID 26858523
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Neutropenia and febrile neutropenia (FN) are frequent and potentially fatal toxicities of myelosuppressive anticancer treatments. The introduction of granulocyte colony-stimulating factors (G-CSFs) in clinical practice has remarkably reduced the duration and severity of neutropenia, as well as the incidence of FN, thus allowing the administration of chemotherapeutic agents at the optimal dose and time with lower risk. The current scenario of G-CSFs in Europe includes filgrastim, lenograstim, some G-CSF biosimilars, and pegfilgrastim. Recently, a novel long-acting G-CSF, lipegfilgrastim, became available. Lipegfilgrastim is a glycopegylated G-CSF, alternative to pegfilgrastim, and has shown in randomized trials, to be equivalent to pegfilgrastim in reducing the incidence of severe neutropenia and FN in patients with breast cancer receiving chemotherapy, with a similar safety profile. Furthermore, lipegfilgrastim was more effective than the placebo in reducing the incidence of severe neutropenia, its duration, and time to absolute neutrophil count recovery, in patients with non-small cell lung cancer receiving myelosuppressive therapy. Although the number of studies currently published is still limited, lipegfilgrastim seems to be a promising drug in the management of chemotherapy-induced neutropenia.

Citing Articles

Improving the Therapeutic Potential of G-CSF through Compact Circular PEGylation Based on Orthogonal Conjugations.

Grigoletto A, Marotti V, Tedeschini T, Campara B, Marigo I, Ingangi V Biomacromolecules. 2023; 24(9):4229-4239.

PMID: 37638739 PMC: 10498445. DOI: 10.1021/acs.biomac.3c00543.


Semimechanistic pharmacokinetic-pharmacodynamic model of tripegfilgrastim for pediatric patients after chemotherapy.

Lee S, Hong K, Jang I, Yu K, Kang H, Oh J CPT Pharmacometrics Syst Pharmacol. 2023; 12(9):1319-1334.

PMID: 37559343 PMC: 10508573. DOI: 10.1002/psp4.13012.


An observational study of dose dense chemotherapy with lipegfilgrastim support in early breast cancer.

Rashed A, Fitzpatrick O, Easty D, Coyne Z, Collins D, Mallet V BMC Cancer. 2023; 23(1):171.

PMID: 36803350 PMC: 9942277. DOI: 10.1186/s12885-023-10603-0.


New insight into strategies used to develop long-acting G-CSF biologics for neutropenia therapy.

Theyab A, Alsharif K, Alzahrani K, Oyouni A, Hawsawi Y, Algahtani M Front Oncol. 2023; 12:1026377.

PMID: 36686781 PMC: 9850083. DOI: 10.3389/fonc.2022.1026377.


Pooled Analysis on the Effectiveness and Safety of Lipegfilgrastim in Patients With Urological Malignancies in the Real-World Setting.

Merseburger A, Geiges G, Klier J, Wiesholzer M, Pichler P Front Oncol. 2021; 11:655355.

PMID: 34123810 PMC: 8195268. DOI: 10.3389/fonc.2021.655355.


References
1.
Radosavljevic D, Golubicic I, Gavrilovic D, Kezic I, Jelic S . Do the time to chemotherapy response and the dose intensity have an impact on patient outcome in advanced non-small cell lung cancer?. J BUON. 2009; 14(2):203-9. View

2.
Ratti M, Tomasello G . Lipegfilgrastim for the prophylaxis and treatment of chemotherapy-induced neutropenia. Expert Rev Clin Pharmacol. 2014; 8(1):15-24. DOI: 10.1586/17512433.2015.984688. View

3.
Gregory S, Trumper L . Chemotherapy dose intensity in non-Hodgkin's lymphoma: is dose intensity an emerging paradigm for better outcomes?. Ann Oncol. 2005; 16(9):1413-24. DOI: 10.1093/annonc/mdi264. View

4.
Hoggatt J, Pelus L . New G-CSF agonists for neutropenia therapy. Expert Opin Investig Drugs. 2013; 23(1):21-35. DOI: 10.1517/13543784.2013.838558. View

5.
Trillet-Lenoir V, Green J, Manegold C, von Pawel J, Gatzemeier U, Lebeau B . Recombinant granulocyte colony stimulating factor reduces the infectious complications of cytotoxic chemotherapy. Eur J Cancer. 1993; 29A(3):319-24. DOI: 10.1016/0959-8049(93)90376-q. View