TY - JOUR
T1 - Comparison between a single dose of PEG G-CSF and multiple doses of non-PEG G-CSF
T2 - a systematic review and meta-analysis from Clinical Practice Guidelines for the use of G-CSF 2022
AU - Yoshinami, Tetsuhiro
AU - Nozawa, Kazuki
AU - Yokoe, Takamichi
AU - Ozaki, Yukinori
AU - Nishio, Hiroshi
AU - Tsuchihashi, Kenji
AU - Ichihara, Eiki
AU - Miura, Yuji
AU - Endo, Makoto
AU - Yano, Shingo
AU - Maruyama, Dai
AU - Susumu, Nobuyuki
AU - Takekuma, Munetaka
AU - Motohashi, Takashi
AU - Ito, Mamoru
AU - Baba, Eishi
AU - Ochi, Nobuaki
AU - Kubo, Toshio
AU - Uchino, Keita
AU - Kimura, Takahiro
AU - Kamiyama, Yutaro
AU - Nakao, Shinji
AU - Tamura, Shinobu
AU - Nishimoto, Hitomi
AU - Kato, Yasuhisa
AU - Sato, Atsushi
AU - Takano, Toshimi
N1 - Publisher Copyright:
© The Author(s) under exclusive licence to Japan Society of Clinical Oncology 2024.
PY - 2024/6
Y1 - 2024/6
N2 - Backgroud: Granulocyte colony-stimulating factor (G-CSF) is widely used for the primary prophylaxis of febrile neutropenia (FN). Two types of G-CSF are available in Japan, namely G-CSF chemically bound to polyethylene glycol (PEG G-CSF), which provides long-lasting effects with a single dose, and non-polyethylene glycol-bound G-CSF (non-PEG G-CSF), which must be sequentially administrated for several days. Methods: This current study investigated the utility of these treatments for the primary prophylaxis of FN through a systematic review of the literature. A detailed literature search for related studies was performed using PubMed, Ichushi-Web, and the Cochrane Library. Data were independently extracted and assessed by two reviewers. A qualitative analysis or meta-analysis was conducted to evaluate six outcomes. Results: Through the first and second screenings, 23 and 18 articles were extracted for qualitative synthesis and meta-analysis, respectively. The incidence of FN was significantly lower in the PEG G-CSF group than in the non-PEG G-CSF group with a strong quality/certainty of evidence. The differences in other outcomes, such as overall survival, infection-related mortality, the duration of neutropenia (less than 500/μL), quality of life, and pain, were not apparent. Conclusions: A single dose of PEG G-CSF is strongly recommended over multiple-dose non-PEG G-CSF therapy for the primary prophylaxis of FN.
AB - Backgroud: Granulocyte colony-stimulating factor (G-CSF) is widely used for the primary prophylaxis of febrile neutropenia (FN). Two types of G-CSF are available in Japan, namely G-CSF chemically bound to polyethylene glycol (PEG G-CSF), which provides long-lasting effects with a single dose, and non-polyethylene glycol-bound G-CSF (non-PEG G-CSF), which must be sequentially administrated for several days. Methods: This current study investigated the utility of these treatments for the primary prophylaxis of FN through a systematic review of the literature. A detailed literature search for related studies was performed using PubMed, Ichushi-Web, and the Cochrane Library. Data were independently extracted and assessed by two reviewers. A qualitative analysis or meta-analysis was conducted to evaluate six outcomes. Results: Through the first and second screenings, 23 and 18 articles were extracted for qualitative synthesis and meta-analysis, respectively. The incidence of FN was significantly lower in the PEG G-CSF group than in the non-PEG G-CSF group with a strong quality/certainty of evidence. The differences in other outcomes, such as overall survival, infection-related mortality, the duration of neutropenia (less than 500/μL), quality of life, and pain, were not apparent. Conclusions: A single dose of PEG G-CSF is strongly recommended over multiple-dose non-PEG G-CSF therapy for the primary prophylaxis of FN.
KW - Meta-analysis
KW - Multiple doses
KW - Non-PEG G-CSF
KW - PEG G-CSF
KW - Single dose
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U2 - 10.1007/s10147-024-02504-4
DO - 10.1007/s10147-024-02504-4
M3 - Article
C2 - 38649648
AN - SCOPUS:85191032810
SN - 1341-9625
VL - 29
SP - 681
EP - 688
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 6
ER -