Literature DB >> 23444969

Pegfilgrastim prophylaxis in patients at different levels of risk for chemotherapy-associated febrile neutropenia: an observational study.

Michael Fiegl1, Günther G Steger, Michael Studnicka, Wolfgang Eisterer, Christine Jaeger, Wolfgang Willenbacher.   

Abstract

BACKGROUND: Guidelines for using granulocyte colony-stimulating factor (G-CSF) in patients receiving chemotherapies with 10-20% (intermediate) risk for febrile neutropenia (FN) recommend additional assessment of patient-related FN risk factors.
OBJECTIVE: The current study evaluated adherence to guideline recommendations and analysed modalities of pegfilgrastim use.
METHODS: Adult cancer patients scheduled to receive a chemotherapy regimen assessed by the investigators as intermediate FN risk and who received pegfilgrastim were prospectively enrolled in this observational study from 2007-2010. Risk factors at study entry, treatment modalities and FN assessment were documented by investigators, whereas guideline adherence was centrally checked in a post-hoc analysis, according to guideline categorizations.
RESULTS: Thirty-seven centres enrolled 335 evaluable patients with solid and hematologic neoplasias. Although physicians initially rated the FN risk of all chemotherapies as intermediate, after central re-assessment this applied only to 63.9% of regimens; 21.2% were reassessed as low risk and 14.9% as high risk. Pegfilgrastim was used as primary prophylaxis in 80.3% of all patients. The most frequent FN risk factors considered by physicians when deciding to use pegfilgrastim were female gender, advanced disease, age ≥ 65 years, and anaemia. FN incidence was higher in patients with ≥ 4 FN risk factors than those with <4 risk factors (10% vs. 4.3%; p = 0.055) and in patients with severe comorbidity than those without (13.6% vs. 4.5%; p = 0.014). Overall FN rate was 5.7%. LIMITATIONS: Due to the observational design of the study, findings are descriptive in nature. Post-hoc assessment of chemotherapy FN risk was determined by author's opinion in some cases.
CONCLUSIONS: Overall, there was good adherence of Austrian physicians to guideline recommendations; however, there are chemotherapy regimens and clinical settings in which FN risk assignment is unclear in the literature. FN incidence with pegfilgrastim prophylaxis was similar to that reported in other observational and randomized studies.

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Year:  2013        PMID: 23444969     DOI: 10.1185/03007995.2013.781018

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  8 in total

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Authors:  Ken Sasaki; Kensuke Matsuda; Masashi Miyauchi; Akira Honda; Arika Shimura; Yosuke Masamoto; Mineo Kurokawa
Journal:  Ann Hematol       Date:  2021-03-30       Impact factor: 3.673

2.  Pegteograstim prophylaxis for chemotherapy-induced neutropenia and febrile neutropenia: a prospective, observational, postmarketing surveillance study in Korea.

Authors:  Jaekyung Cheon; Hyeon-Su Im; Ho-Jin Shin; Inho Kim; Won Sik Lee; Kyung-Hun Lee; Seong Kyu Park; Min Kyoung Kim; Un Jong Choi; Jung Han Kim; IlKyun Lee; Jae-Cheol Jo
Journal:  Support Care Cancer       Date:  2021-03-08       Impact factor: 3.603

3.  Evaluating the safety and effectiveness of PegaGen® (pegfilgrastim) for the prevention of chemotherapy-induced febrile neutropenia: a post-marketing surveillance study.

Authors:  Arash Jenabian; Ali Ehsanpour; Seyed Mohammad Reza Mortazavizadeh; Jahangir Raafat; Mohsen Razavi; Adnan Khosravi; Sharareh Seifi; Babak Salimi; Nassim Anjidani; Hamidreza Kafi
Journal:  Support Care Cancer       Date:  2022-07-06       Impact factor: 3.359

4.  Febrile neutropenia (FN) and pegfilgrastim prophylaxis in breast cancer and non-Hodgkin's lymphoma patients receiving high (> 20%) FN-risk chemotherapy: results from a prospective observational study.

Authors:  Jean Paul Salmon; Martin Smakal; Charisios Karanikiotis; Marek Z Wojtukiewicz; Yohann Omnes; Lucy DeCosta; Sally Wetten; James O'Kelly
Journal:  Support Care Cancer       Date:  2018-09-26       Impact factor: 3.603

5.  Overuse and underuse of pegfilgrastim for primary prophylaxis of febrile neutropenia.

Authors:  Andrew R Zullo; Uvette Lou; Sarah E Cabral; Justin Huynh; Christine M Berard-Collins
Journal:  J Oncol Pharm Pract       Date:  2018-08-19       Impact factor: 1.809

6.  Safety and tolerability of Peg-grafeel, a pegfilgrastim, for the prophylactic treatment of chemotherapy-induced neutropenia and febrile neutropenia: A prospective, observational, postmarketing surveillance study in India.

Authors:  Vineet Talwar; Sharanabasappa S Nirni; Krishna Mohan Mallavarapu; Anupama Ramkumar; Nitu Sinha
Journal:  South Asian J Cancer       Date:  2017 Jan-Mar

7.  Results of a prospective dose intensity and neutropenia prophylaxis evaluation programme (DIEPP) in cancer patients at risk of febrile neutropenia due to myelosuppressive chemotherapy.

Authors:  Radosław Mądry; Lidia Popławska; Ferdinand Haslbauer; Martin Šafanda; Doru Ghizdavescu; Jana Benkovicova; Tibor Csőszi; Georgi Mihaylov; Daniela Niepel; Christine Jaeger; Iveta Frkanova; Alina Macovei; Christine Staudigl
Journal:  Wien Klin Wochenschr       Date:  2016-01-08       Impact factor: 1.704

8.  Multicentre, Prospective Observational Study of Pegfilgrastim Primary Prophylaxis in Patients at High Risk of Febrile Neutropenia in Poland: PROFIL Study.

Authors:  Wojciech Jurczak; Ewa Kalinka-Warzocha; Ewa Chmielowska; Renata Duchnowska; Elzbieta Wojciechowska-Lampka; Karolina Wieruszewska
Journal:  Contemp Oncol (Pozn)       Date:  2015-07-08
  8 in total

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